Source: ClinicalTrials.gov — U.S. National Library of Medicine — A database of privately and publicly funded clinical studies conducted around the world (U.S. National Library of Medicine, public domain).
This page lists clinical trials related to Spine Injuries and Disorders from the ClinicalTrials.gov database.
Trial Summary
- Total studies: 50
- Recruiting: 17
- Active, not recruiting: 10
- Completed: 13
- Other: 10
Results are refreshed periodically and may not reflect the most current information available from ClinicalTrials.gov.
Recruiting Trials
NCT04937868 — Developing a Decision Instrument to Guide Abdominal-pelvic CT Imaging of Blunt Trauma Patients
| Status | Recruiting |
| Phase | N/A |
| Sponsor | University of California, Los Angeles |
| Enrollment | 12000 |
| Study Type | OBSERVATIONAL |
| Conditions | Abdominal Injury; Pelvic Fracture; Genital Hemorrhage; Lumbar Spine Injury; Hip Injuries |
| Interventions |
Unrecognized abdominal and pelvic injuries can result in catastrophic disability and death. Sporadic reports of “occult” injuries have generated concern, and physicians, fearing that they may miss such an injury, have adopted the practice of obtaining computed tomography on virtually all patients with significant blunt trauma. This practice exposes large numbers patients to dangerous radiation …
NCT04639297 — NeuroVision vs Standard Neuromonitoring
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Rush University Medical Center |
| Enrollment | 148 |
| Study Type | INTERVENTIONAL |
| Conditions | Neurologic Deficits |
| Interventions | ; |
The purpose of this study is to perform a prospective, randomized, controlled clinical trial to assess the utility of IONM in patients undergoing primary, single or multilevel lateral spinal procedures. Subjects will be randomized to undergo a lateral spine surgery with the use of NeuroVision® IONM or conventional hospital based IONM to assess incidence of new-onset neurological injury.
NCT05296889 — Post-Market Clinical Follow-Up Study on the Safety and Performance of Ennovate® Cervical
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Aesculap AG |
| Enrollment | 200 |
| Study Type | OBSERVATIONAL |
| Conditions | Spine Fracture; Degenerative Disc Disease; Spinal Instability; Spinal Tumor; Degenerative Myelopathy |
| Interventions |
Multicenter Post market clinical follow-up Study on the Safety and Performance of Ennovate® Cervical - Prospective, pure data collection of all Ennovate Cervical patients in Total Indications
NCT05023772 — Laser Interstitial Thermal Ablation and Stereotactic Radiosurgery for Patients With Spine Metastases
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Henry Ford Health System |
| Enrollment | 60 |
| Study Type | INTERVENTIONAL |
| Conditions | Neoplasm Metastasis; Spinal Cord Diseases; Spinal Cord Compression; Spinal Cord Tumor; Spine Metastases |
| Interventions | ; ; |
The purpose of this research is to combine two complementary modes of treatment, spinal interstitial laser ablation and stereotactic spine radiosurgery (SSRS) for the treatment for spinal tumors near the spinal cord with an objective to improve tumor control, improve pain control, preserve function, and improve quality of life. We will also assess how effective these combined modes of treatment…
NCT05170815 — Clariance ErYs Registry
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Clariance |
| Enrollment | 760 |
| Study Type | OBSERVATIONAL |
| Conditions | Spine Degeneration; Spine Spondylosis Thoracic; Spinal Deformity; Spinal Tumor; Spinal Fracture |
| Interventions |
International, prospective, single arm, multicenter and observational Post-Market Clinical Follow-up (PMCF).
The overall objective of this study is to collect preoperative, intraoperative and postoperative (at 9 weeks, 6 months, 1 year and 2 years) data on the clinical complications and functional outcomes of the study devices to demonstrate safety and performance in a real-world setting.
The…
NCT05856370 — The Ailliance Post-Market Clinical Study
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Medtronic Spinal and Biologics |
| Enrollment | 1000 |
| Study Type | INTERVENTIONAL |
| Conditions | Spinal Deformity; Spinal Degenerative Disorder; Spinal Fusion Failure; Spinal Trauma; Spinal Tumor Case |
| Interventions |
The purpose of this clinical study is to collect performance and safety data for post-market Medtronic devices indicated for cranial and/or spinal indication(s).
Subjects are enrolled and followed postoperatively to 24 months. The Ailliance clinical study is intended to collect data congruous with routine clinical care practices.
NCT05856539 — ESP Block in MIS Lumbar Spine Surgery
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Hospital for Special Surgery, New York |
| Enrollment | 48 |
| Study Type | INTERVENTIONAL |
| Conditions | Patients With Spinal Stenosis Indicated for MIS TLIF |
| Interventions |
This is a prospective, randomized controlled trial of patients undergoing minimally invasive transforaminal lumbar interbody fusion. This study will randomize patients into one of two groups: erector spinae plane (ESP) block and no ESP block.
NCT05665998 — Brain Controlled Spinal Cord Stimulation in Participants With Cervical Spinal Cord Injury for Upper Limb Rehabilitation
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Ecole Polytechnique Fédérale de Lausanne |
| Enrollment | 3 |
| Study Type | INTERVENTIONAL |
| Conditions | Cervical Spinal Cord Injury; Tetraplegia |
| Interventions |
Cervical spinal cord stimulation can elicit arm and hand movements through recruitment of proprioceptive neurons in the dorsal roots. In participants with cervical spinal cord injury, the spare roots bellow the lesion can be used to reactivate motor function. Decoding of motor intentions can be achieved through implantable electrocorticography (ECoG) devices.
In this study, the investigators w…
NCT07627282 — Evaluation of the Evolution of Patient Care Within the Spinal Pathology Department
| Status | Recruiting |
| Phase | N/A |
| Sponsor | University Hospital, Bordeaux |
| Enrollment | 15000 |
| Study Type | INTERVENTIONAL |
| Conditions | Spinal Stenosis; SPINAL Fracture; Vertebral Osteomyelitis; Vertebral Metastasis |
| Interventions |
Spinal conditions are a major public health issue. Their management by surgical treatment is constantly improving and surgical procedures or implantable medical devices are experiencing significant progress. These innovations have not yet all been precisely evaluated but have already led to significant changes in care practices. The primary objective of our study is to describe, via an exhausti…
NCT06293157 — Carbon Fiber Transpedicular Screws in Treatment of Spinal Metastatic Disease
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Copernicus Memorial Hospital |
| Enrollment | 226 |
| Study Type | INTERVENTIONAL |
| Conditions | Metastatic Spinal Cord Compression; Metastasis Spine |
| Interventions | ; ; |
Background: Spinal metastatic disease constitute a serious clinical problem in oncology. Bones are the third most common organ where metastases are located, and the spine is the place where they are most often located. Due to the complexity of the clinical problem, metastatic spine disease remains of interest to many medical specialties: neurosurgery, orthopedics, clinical oncology, radiotherap…
NCT06502951 — Manipulation and Dry Needling in Patients With Cervicogenic Headache and WAD II
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Alabama Physical Therapy & Acupuncture |
| Enrollment | 120 |
| Study Type | INTERVENTIONAL |
| Conditions | Cervicogenic Headache; Whiplash Injuries |
| Interventions | ; |
The purpose of this research is to compare two different approaches for treating patients with cervicogenic headaches associated with type II whiplash associated disorder: non-thrust mobilization and exercise versus thrust manipulation and dry needling. Physical therapists commonly use all of these techniques to treat cervicogenic headaches. This study is attempting to find out if one treatment…
NCT06736106 — Which Markers of Musculoskeletal Health Can Explain Complications in Spinal Surgery?
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Istituto Ortopedico Rizzoli |
| Enrollment | 200 |
| Study Type | INTERVENTIONAL |
| Conditions | Spine Injuries and Disorders |
| Interventions |
The present study is related to the project “ORTHOSPINE FITNESS: WHICH MARKERS OF MUSCULOSKELETAL HEALTH CAN EXPLAIN COMPLICATIONS IN SPINE SURGERY?”, winner of the Ministry of Health Call, financed by the European Union, “M6/C2_CALL 2023”, Project Code " PNRR- MCNT2-2023-12378098", Call section “Non-chronic chronic diseases transmissible diseases (MCnT2) with a high impact on health systems”….
NCT06704906 — Adult Patient Outcomes After Spine Surgery With Fibergraft BG Putty/Viper Prime
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Nitin Agarwal |
| Enrollment | 100 |
| Study Type | OBSERVATIONAL |
| Conditions | Spondylolisthesis, Lumbar Region; Spinal Trauma With Neurological Deficit; Degeneration of Lumbar Intervertebral Disc |
| Interventions |
The Viper Prime/Expedium spine systems are intended to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of acute and chronic instabilities or deformities of the thoracolumbar and sacral spine. The Fibergraft Bioactive Glass (BG) is engineered to mimic the body’s natural bone healing process. While previous studies…
NCT06407427 — Evaluating the Efficacy of a Mobile Application in Postoperative Rehabilitation
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Yale University |
| Enrollment | 100 |
| Study Type | INTERVENTIONAL |
| Conditions | Spine Degeneration; Hip Arthritis; Knee Osteoarthritis; Hip Fractures |
| Interventions | ; |
This study aims to evaluate the effectiveness of a mobile application in improving postoperative rehabilitation outcomes among patients undergoing orthopedic surgery.
NCT07219108 — Transcutaneous Auricular Vagus Enhanced Recovery in the NeuroICU
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Washington University School of Medicine |
| Enrollment | 160 |
| Study Type | INTERVENTIONAL |
| Conditions | Acute Neurological Injury; Acute Medical Conditions |
| Interventions | ; |
This study will demonstrate the impact of taVNS on reducing adverse events in NeuroICU patients, determine if taVNS reduces length of stay, and quantify the economic benefits of taVNS implementation in a broader neurocritical care population.
NCT07225101 — Evaluation of the Efficacy of STRATAFIX for Neurosurgical Cranial and Spine Procedures
| Status | Recruiting |
| Phase | Phase 4 |
| Sponsor | University of Michigan |
| Enrollment | 160 |
| Study Type | INTERVENTIONAL |
| Conditions | Wound Closure; Brain Tumor Adult; Spine; Neurovascular; Hemorrhagic Stroke, Intracerebral |
| Interventions |
This research is studying a device already approved by the Food and Drug Administration (FDA) to treat wound closures. Researchers are studying a large group of people to continue to learn information about the safety of the STRATAFIX suture and how people’s bodies react to using it over a long period of time. This research will provide additional information about using STRATAFIX sutures to cl…
NCT06867809 — Spine and Brain Stimulation for Movement Recovery After Cervical Spinal Cord Injury
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Jason Carmel |
| Enrollment | 20 |
| Study Type | INTERVENTIONAL |
| Conditions | Spinal Cord Injury; Spinal Cord Injury Cervical |
| Interventions |
Stimulation of the spinal cord and brain represents a new experimental therapy that may have potential to restore movement after spinal cord injury. While some scientists have begun to study the effect of electrical stimulation on patient’s ability to walk and move their legs after lower spinal cord injury, the use of stimulation of the upper (cervical) spine to restore arm and hand function af…
Active, Not Recruiting
NCT01409954 — Collecting Bone Graft During Spinal Decompression and Posterolateral Lumbar Fusion to Better Define Bone Making Cells
| Status | Active, not recruiting |
| Phase | N/A |
| Sponsor | University of Utah |
| Enrollment | 60 |
| Study Type | OBSERVATIONAL |
| Conditions | Pseudarthrosis After Fusion or Arthrodesis |
The purpose of this study is to improve fusion (bony healing) techniques and improve patient recovery by identifying cells in your body that make bone. Patients with spine problems often need surgeries that include fusion (bony healing) of vertebrae (bones in your back) together in order to hold the bones steady allowing them to heal together (fusion). If the vertebrae (back bones) fail to heal…
NCT02713269 — Thermal Ablation and Spine Stereotactic Radiosurgery in Treating Patients With Spine Metastases at Risk for Compressing the Spinal Cord
| Status | Active, not recruiting |
| Phase | Phase 2 |
| Sponsor | M.D. Anderson Cancer Center |
| Enrollment | 60 |
| Study Type | INTERVENTIONAL |
| Conditions | Malignant Digestive System Neoplasm; Metastatic Head and Neck Carcinoma; Metastatic Kidney Carcinoma; Metastatic Malignant Neoplasm in the Spine; Metastatic Malignant Neoplasm of Unknown Primary |
| Interventions | ; ; |
This phase II clinical trial studies how well thermal ablation and spine stereotactic radiosurgery work in treating patients with cancer that has spread to the spine (spine metastases) and is at risk for compressing the spinal cord. Thermal ablation uses a laser to heat tumor tissue and helps to shrink the tumor by destroying tumor cells. Stereotactic radiosurgery delivers a large dose of radia…
NCT05589402 — Temporary Inactivation of Strong Muscle Sensation to Improve Rehabilitation Interventions in SCI
| Status | Active, not recruiting |
| Phase | Phase 1 |
| Sponsor | University of Texas Rio Grande Valley |
| Enrollment | 30 |
| Study Type | INTERVENTIONAL |
| Conditions | Spinal Cord Injuries; Spine Disease; Stroke |
| Interventions | ; |
The investigators are conducting a research study to try to improve rehabilitation interventions for individuals with spinal cord injury (SCI). In this study, the aim is to determine if temporarily numbing non-paralyzed arm muscles with an over-the-counter numbing cream while exercising paralyzed muscles, can improve the strength, function, and sensation of paralyzed muscles after a spinal cord…
NCT03956537 — PMCF Neo Pedicle Screw and Cage Systems
| Status | Active, not recruiting |
| Phase | N/A |
| Sponsor | Neo Medical SA |
| Enrollment | 150 |
| Study Type | OBSERVATIONAL |
| Conditions | Degenerative Disc Disease; Spondylolisthesis; Spinal Stenosis; Spinal Tumor; Trauma |
| Interventions | ; |
The objectives of this clinical observational study is to evaluate the safety and efficacy (performance) of the Neo Pedicle Screw System™ and the Neo Cage System™ interbody fusion device. To demonstrate non-inferiority of safety and function to an historical control from the published medical literature on competitive devices.
NCT04302259 — Intelligent Spine Interface, Clinical (ISI-C)
| Status | Active, not recruiting |
| Phase | N/A |
| Sponsor | Rhode Island Hospital |
| Enrollment | 3 |
| Study Type | INTERVENTIONAL |
| Conditions | Spinal Cord Injury |
| Interventions |
This research study is being done to test a new device developed for spinal cord injury (SCI) patients. The purpose of this study is to collect data on how the nervous system signals travel within the spinal cord of SCI patients. Once the investigators understand that, they hope to develop a device that may help rehabilitation of SCI patients so that they can regain function in their lower limb…
NCT05082090 — A Multi-Center Post-Market Data Collection Protocol to Evaluate the Performance of Orthofix Spine Devices
| Status | Active, not recruiting |
| Phase | N/A |
| Sponsor | Orthofix Inc. |
| Enrollment | 2000 |
| Study Type | OBSERVATIONAL |
| Conditions | Spinal Disorders/Injuries |
| Interventions |
This protocol is designed to study Orthofix regulatory approved and commercially available spine devices to generate Real World Evidence (RWE) of device safety and performance in the treatment of patients with spine injuries and/or disorders following the local medical standard of care. The clinical data generated from this study will support compliance to global regulatory requirements includi…
NCT06243952 — Brain Controlled Spinal Cord Stimulation In Participants With Spinal Cord Injury For Lower Limb Rehabilitation
| Status | Active, not recruiting |
| Phase | N/A |
| Sponsor | Ecole Polytechnique Fédérale de Lausanne |
| Enrollment | 3 |
| Study Type | INTERVENTIONAL |
| Conditions | Spinal Cord Injuries; Paraplegia |
| Interventions |
The purpose of this clinical study is to evaluate the preliminary safety and effectiveness of using a cortical recording device (ECoG) combined with lumbar targeted epidural electrical stimulation (EES) of the spinal cord to restore voluntary motor functions of lower limbs in participants with chronic spinal cord injury suffering from mobility impairment.
The goal is to establish a direct brid…
NCT06525896 — Non-surgical Spinal Decompression Therapy and Outcomes
| Status | Active, not recruiting |
| Phase | N/A |
| Sponsor | University of South Florida |
| Enrollment | 42 |
| Study Type | INTERVENTIONAL |
| Conditions | Low Back Pain; Herniation, Disc; Sciatic Radiculopathy; Intervertebral Disc Stenosis of Neural Canal; Intervertebral Disc Injury |
| Interventions | ; |
This project will determine the clinical utility of non-surgical spine decompression for chronic low back pain (LBP). LBP is one of the highest incidence medical conditions that contributes to disability, decreased activities of daily living, decreased quality of life, and inability to work. LBP affects ≈70-85% of people during their lifetime, with ≈20% becoming chronic by age 20-59 years. Many…
NCT06778551 — Shoulder School: A Multicenter Prospective Randomized Controlled Study
| Status | Active, not recruiting |
| Phase | N/A |
| Sponsor | Sandra Jiménez-del-Barrio |
| Enrollment | 40 |
| Study Type | INTERVENTIONAL |
| Conditions | Subacromial Impingement Syndrome |
| Interventions | ; |
Subacromial impingement syndrome (SIS) is the most common cause of shoulder pain. Patients with SIS present with localized shoulder pain, sometimes nocturnal, which leads to a decrease in shoulder strength and function, significantly affecting their quality of life. Several authors have proposed that reduced scapular movement could be a direct causal mechanism for the symptoms associated with S…
NCT07667426 — Evaluation of Osteopathic Protocol on Rachialgia, Bis
| Status | Active, not recruiting |
| Phase | N/A |
| Sponsor | Cabinet d’ostéopathie Michel Boeuf |
| Enrollment | 50 |
| Study Type | INTERVENTIONAL |
| Conditions | Spine Injuries and Disorders |
| Interventions |
Rachialgia are among the most common reasons for consultation with the general practitioner in Europe. Most of the guidelines recommend spinal manipulation. This study attempts to propose a solution with 2 parts: tests of induced pain that have a greater sensitivity than palpatory tests of movements and a comprehensive musculoskeletal treatment protocol. The objective of this bicentric study is…
Not Yet Recruiting
NCT06552507 — The Outcome of Injured Cervical Spinal Cord with Uncontrolled Swelling Under Duraplasty
| Status | Not yet recruiting |
| Phase | N/A |
| Sponsor | Chang Gung Memorial Hospital |
| Enrollment | 104 |
| Study Type | INTERVENTIONAL |
| Conditions | Spine Injury; Cord Injury, Spinal; Cord Infarction Spinal; Incomplete Spinal Cord Injury; Complete Spinal Cord Injury |
| Interventions |
Overall Objective: To assess whether incorporating duraplasty alongside bony decompression enhances motor function outcomes in individuals following Traumatic Spinal Cord Injury (TSCI).
Rationale for Research:
In a systematic review, individuals suffering from cervical Traumatic Spinal Cord Injuries (TSCIs) identified specific priorities for improvement in their quality of life. These priorit…
NCT06882239 — SPINEPASS: SPINE Self-management Techniques for Persistent Headache After Concussion: Physical Therapy Targeting Autonomic and Dura Mater Function.
| Status | Not yet recruiting |
| Phase | N/A |
| Sponsor | The University of Queensland |
| Enrollment | 120 |
| Study Type | INTERVENTIONAL |
| Conditions | Persistent Post-concussive Symptoms; Post Traumatic Headache |
| Interventions | ; |
This is a prospective randomized controlled trial comparing two different physical therapy approaches to the treatment of posttraumatic headache with autonomic symptoms. AIM 1: To establish the efficacy of SPINEPASS against Standard Physical Therapy to reduce headache disability and impact amongst patients with persistent post-concussion headache. AIM 2: Demonstrate the superiority of SPINEPASS…
NCT07402733 — Psychologically Informed Cervicovestibular Rehabilitation (PIC Rehab) for Mild Traumatic Brain Injury: A Feasibility Trial
| Status | Not yet recruiting |
| Phase | Phase 1 |
| Sponsor | Sport Injury Prevention Research Centre |
| Enrollment | 34 |
| Study Type | INTERVENTIONAL |
| Conditions | Mild Traumatic Brain Injury, Concussion |
| Interventions | ; |
Mild traumatic brain injuries (“mTBIs”) affect over 480,000 Canadians each year. While many individuals recover in the initial 4 weeks following mTBI, in up to 30% of individuals symptoms and functional impairments often persist leading to significant disability, decreased quality of life and participation in education, physical and occupational related activities. An assessment that evaluates …
NCT07577726 — Prospective Observational Multimodal Neuromonitoring During High-Risk Adult Surgery
| Status | Not yet recruiting |
| Phase | N/A |
| Sponsor | University of Texas Southwestern Medical Center |
| Enrollment | 300 |
| Study Type | OBSERVATIONAL |
| Conditions | Postoperative Cognitive Complications; Delirium; Perioperative/Postoperative Complications; Brain Injuries; Anesthesia |
This is a prospective observational cohort study of adult patients undergoing high-risk surgery at UT Southwestern Medical Center. The study acquires synchronized multimodal neuromonitoring data - including SedLine quantitative EEG (qEEG) extracted from standard-of-care clinical monitoring and, where deployed, Brain4Care (B4C) noninvasive intracranial dynamics data - and links these data to per…
NCT07367139 — Occupational Exposure to Whole Body Vibration Among U.S. Military Veterans: Acute and Chronic Contributions to Musculoskeletal Disorders and Spine-Area Pain
| Status | Not yet recruiting |
| Phase | N/A |
| Sponsor | Milwaukee VA Medical Center |
| Enrollment | 112 |
| Study Type | INTERVENTIONAL |
| Conditions | Spine Health; Spine Injuries and Disorders; Spine Degeneration; Whole Body Vibration |
| Interventions |
Significance to VA: There is a lack of prospective longitudinal studies investigating the relationship between risk factors to Veterans and development and progression of musculoskeletal (MSK) spine injury and pain. Military operational exposure to whole body vibration (WBV) is known to contribute to MSK disorders and pain. Our preliminary studies identified accelerated lumbar and cervical spin…
Enrolling by Invitation
NCT04565366 — Transforming Research and Clinical Knowledge in Spinal Cord Injury
| Status | Enrolling by invitation |
| Phase | N/A |
| Sponsor | University of California, San Francisco |
| Enrollment | 726 |
| Study Type | OBSERVATIONAL |
| Conditions | Spinal Cord Injuries |
The overall goal of Transforming Research and Clinical Knowledge in Spinal Cord Injury (TRACK-SCI) study is to determine the relationships among the clinical, neuroimaging, cognitive, genetic and proteomic biomarker characteristics of acute traumatic spinal cord injury (SCI). TRACK-SCI seeks to combine high quality care variables with high density physiology data collection to better understand…
NCT04770571 — Posterior Cervical Fixation Study
| Status | Enrolling by invitation |
| Phase | N/A |
| Sponsor | NuVasive |
| Enrollment | 150 |
| Study Type | OBSERVATIONAL |
| Conditions | Degenerative Disc Disease; Craniocervical Injuries; Cervical Radiculopathy; Cervical Disc Disease; Cervical Fusion |
| Interventions |
The objective of this study is to evaluate the safety and performance of occipito-cervico-thoracic spine surgery using posterior fixation as measured by reported complications, radiographic outcomes, and patients reported outcomes (PROs).This study is being undertaken to identify possible residual risks and to clarify mid-to long-term clinical performance that may affect the benefit/risk ratio …
Completed Trials
NCT00825422 — Local Anesthetic Infiltration to Prevent Postoperative Pain After Lumbar Surgery
| Status | Completed |
| Phase | Phase 3 |
| Sponsor | University Hospital, Bordeaux |
| Enrollment | 50 |
| Study Type | INTERVENTIONAL |
| Conditions | Hyperalgesia |
| Interventions |
Posterior lumbar arthrodesis causes severe postoperative pain, hampering patients’s postoperative reconvalescence especially functional rehabilitation. Efficient and safe methods for postoperative analgesia are, therefore, mandatory. The application of opioids are the most frequently used therapies for postoperative pain relief but it very often results side effects. Local anesthetic wound infi…
NCT02886260 — Establishing a Descriptive Cohort of Patients Cared for Operation on the Spine
| Status | Completed |
| Phase | N/A |
| Sponsor | Centre Hospitalier Universitaire de Nīmes |
| Enrollment | 193 |
| Study Type | OBSERVATIONAL |
| Conditions | Quality of Life; Spinal Injuries; Spinal Diseases |
This study aims to:
- describe the monitoring of patients treated for spinal disorders.
- create a comprehensive database of reliable and readily exploitable quickly to produce a library of cross publications between orthopedic surgery and neurosurgical services. This database will include clinical, functional , radiographic , educational, social and professional data.
- obtain a cohort of …
NCT06873074 — A Retrospective Cohort Study About Surgical Efficacy for Lower Cervical Fractures in Ankylosing Spondylitis
| Status | Completed |
| Phase | N/A |
| Sponsor | Zhou Fang |
| Enrollment | 162 |
| Study Type | OBSERVATIONAL |
| Conditions | Ankylosing Spondylitis (AS); Spine Fracture |
| Interventions | ; ; |
The purpose of this retrospective cohort study was to observe and compare the efficacy of anterior cervical long segment fixation, posterior long segment fixation, and combined anterior and posterior fixation for the treatment of cervical vertebral fracture-dislocations in the lower cervical spine in ankylosing spondylitis.
NCT05950360 — Thoracic Spine and Shoulder Kinematics and Muscle Activation in Rock Climbers With Shoulder Pain
| Status | Completed |
| Phase | N/A |
| Sponsor | National Yang Ming Chiao Tung University |
| Enrollment | 37 |
| Study Type | OBSERVATIONAL |
| Conditions | Shoulder Pain; Shoulder Impingement Syndrome |
| Interventions |
Background and Purpose: Rock climbing has been a popular sport in recent years. Rock climbing includes various open-chain and closed-chain arm movements. Overhead reaching and pull-up are the basic rock climbing elements heavily involving upper extremities. Different inclination of the wall and terrain also demand sufficient range of motion and strength of the trunk. Generally overhead reaching…
NCT05530798 — CEUS For Intraoperative Spinal Cord Injury
| Status | Completed |
| Phase | N/A |
| Sponsor | Medical University of South Carolina |
| Enrollment | 20 |
| Study Type | INTERVENTIONAL |
| Conditions | Spine Disease; Spinal Stenosis; Spinal Injury; Spinal Cord Diseases; Spinal Cord Injuries |
| Interventions |
Spinal cord injury following posterior decompression in patients suffering from chronic, cervicothoracic spinal cord compression is a known complication with multiple etiologies. Currently, intraoperative neuromonitoring (IONM) remains the gold standard for predicting and preventing post-operative deficits from these procedures. However, there is a paucity in the field of spine surgery for furt…
NCT06900842 — Chronic Pain in Post-Mastectomy Patients; The Difference Between Pectoral Nerve (PECS I-II) and Erector Spinal Plane (ESP) Blocks
| Status | Completed |
| Phase | N/A |
| Sponsor | Hacettepe University |
| Enrollment | 44 |
| Study Type | OBSERVATIONAL |
| Conditions | Breast Cancer Surgery; Postoperative Pain, Acute; Postoperative Pain, Chronic; Post-mastectomy Pain Syndrome; Regional Anesthesia |
This study looks at two types of injections (called PECS and ESP blocks) to see which one works better for reducing pain after breast cancer surgery (mastectomy).
The main question it asks is: Which block is better at reducing pain after surgery - PECS or ESP? Women who had this surgery and received one of the two blocks were followed for three months. We looked at how much pain they felt, how…
NCT06545006 — Effectiveness of a Quick Release Dynamic Muscle-strengthening Program on Dynamic Stabilization of the Cervical Spine
| Status | Completed |
| Phase | N/A |
| Sponsor | University Hospital, Montpellier |
| Enrollment | 50 |
| Study Type | INTERVENTIONAL |
| Conditions | Rugby; Craniocerebral Trauma; Cervical Spine Injury |
| Interventions | ; ; |
The goal of this clinical trial is to learn if Quick Release dynamic strengthening of the cervical spine extensor muscles’ reflex could improve dynamic stabilisation capacities of the cervical spine by reducing muscle activation delay in amateurs rugby players. The main questions it aims to answer are described as follows:
The primary outcome measure is the comparison between the intervention …
NCT06950411 — Validation of AI Lumbar Spine Anatomy Measureing Function
| Status | Completed |
| Phase | N/A |
| Sponsor | RadiRad Co., Ltd. |
| Enrollment | 150 |
| Study Type | OBSERVATIONAL |
| Conditions | Spinal Cord Compression |
Spinal degeneration and its associated clinical diseases are common ailments in aging societies. With the advent of a super-aging society, the importance of assistive technologies for spinal image interpretation is increasingly significant to enhance care efficiency and reduce medical personnel expenditure. Recently, due to the rapid development of artificial intelligence (AI) algorithm, AI-bas…
NCT06879756 — Relationship Between Flexible Flat Foot and Lumbar Proprioception
| Status | Completed |
| Phase | N/A |
| Sponsor | Cairo University |
| Enrollment | 57 |
| Study Type | OBSERVATIONAL |
| Conditions | Flexible Flatfoot; Lumbar Spine Injury; Proprioceptive Disorders |
The purpose of this study was to determine the relationship between flexible flatfoot and lumbar proprioception.
NCT06650410 — Virtual Intervention for Vertebral frActure: a Pilot, Feasibility Study for a Multicentre Randomized Controlled Trial
| Status | Completed |
| Phase | N/A |
| Sponsor | University of Waterloo |
| Enrollment | 34 |
| Study Type | INTERVENTIONAL |
| Conditions | Osteoporosis; Fractures, Spinal |
| Interventions |
Spine fractures are the most common fracture due to osteoporosis. They happen during falls or activities of daily life, like bending to tie shoes. Fractures of the spine can result in pain, which can sometimes last for a long time. Spine fractures can affect breathing, appetite, digestion, and mobility, and can restrict or modify people’s work or daily activities. There are no standard rehabili…
NCT07155863 — The Effect of Sensory Isolation on Anxiety in Magnetic Resonance Imaging
| Status | Completed |
| Phase | N/A |
| Sponsor | Ege University |
| Enrollment | 72 |
| Study Type | INTERVENTIONAL |
| Conditions | Thorax Injuries; Cervical Injury Spine; Brain Trauma; Joint Trauma |
| Interventions |
The aim of this study is to determine whether the use of earplugs and eye masks in adults reduces anxiety during Manyetic Resonance Imaging. In addition, in order to evaluate the effect of earplugs and eye masks on the physiological symptoms of anxiety, the pulse rate, blood pressure, respiratory rate, and saturation value of adults will be measured before and after imaging.
H0: Earplugs and e…
NCT07340801 — Inter-semispinal Fascial Plane Block (ISPB) Versus Erector Spinae Plane Block (ESPB) in Posterior Cervical Spine Surgery
| Status | Completed |
| Phase | Phase 4 |
| Sponsor | Fayoum University |
| Enrollment | 102 |
| Study Type | INTERVENTIONAL |
| Conditions | Analgesia |
| Interventions |
Recent advances in regional anesthesia techniques have aimed to provide more targeted and effective pain relief. Among these, the erector spinae plane (ESPB) block, the multifidus cervicis plane (MCP) block, and the paraspinal interfascial plane block (PIP) is rapidly expanding in cervical spine surgery. Of these, the inter-semispinal fascial plane block (ISPB) has gained popularity as an analg…
NCT07349719 — Dynamic Compliance-Guided Ventilation in Lumbar Surgery
| Status | Completed |
| Phase | N/A |
| Sponsor | Ankara City Hospital Bilkent |
| Enrollment | 72 |
| Study Type | INTERVENTIONAL |
| Conditions | Lumbar Spine Stenosis; Lumbar Disc Herniation; Ventilator-Induced Lung Injury; Postoperative Complications |
| Interventions | ; |
Postoperative pulmonary complications are a frequent cause of morbidity following lumbar stabilization surgery. Conventional ventilation strategies may not adequately reflect intraoperative changes in respiratory mechanics, potentially leading to impaired postoperative pulmonary function. Dynamic compliance-guided ventilation provides a real-time, individualized approach by adjusting ventilator…
Other (Terminated)
NCT03593330 — Neurosurgical Transitional Care Programme
| Status | Terminated |
| Phase | N/A |
| Sponsor | Barts & The London NHS Trust |
| Enrollment | 242 |
| Study Type | INTERVENTIONAL |
| Conditions | Surgery; Brain Tumor; Brain Tumor, Recurrent; Brain Pathology; Spinal Diseases |
| Interventions |
Readmissions increasingly serve as a metric of hospital performance, inviting quality improvement initiatives in both medicine and surgery. Recently, a readmission reduction program in the United States was associated with significantly shorter length of stay, earlier discharge, and reduced 30-day readmission after elective neurosurgery. These results underscore the importance of patient educat…
NCT05489822 — PMCF Study to Evaluate the VERTICALE® Cervical System in Spine Surgery According to Its Intended Use.
| Status | Terminated |
| Phase | N/A |
| Sponsor | Silony Medical GmbH |
| Enrollment | 4 |
| Study Type | OBSERVATIONAL |
| Conditions | Degenerative Disc Disease (DDD); Instabilities; Trauma; Deformity |
| Interventions |
In accordance with the European Medical Device Regulation MDR 2017/745/EU, the legal manufacturers of medical devices are obliged to evaluate medical devices with regard to their clinical performance and safety.
The VERTICALE® Cervical System is intended for immobilization and stabilization of spinal segments of the craniocervical junction (occipital-C2), subaxial cervical spine (C3-C7) and up…
NCT06616272 — Cervical Spine Focused Treatment for Patients With Persistent Concussion Symptoms and Neck Pain
| Status | Terminated |
| Phase | N/A |
| Sponsor | University of Pittsburgh |
| Enrollment | 2 |
| Study Type | INTERVENTIONAL |
| Conditions | Brain Concussion; Neck Pain |
| Interventions | ; |
Assess the feasibility of recruiting, enrolling and randomizing patients with concussion symptoms and neck pain to receive manual therapy and cervical rehabilitative exercises in addition to standard concussion treatment.
In the usual care workflow provided at the participating concussion clinic, cervical spine rehab is not typically introduced until after week 4. The rationale is that neck pa…