Clinical Trials for Spine Injuries and Disorders

Currently registered clinical trials for Spine Injuries and Disorders from ClinicalTrials.gov. 17 recruiting, 50 total studies.

This content is for informational purposes only. Always consult a healthcare professional.

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

StatusRecruiting
PhaseN/A
SponsorUniversity of California, Los Angeles
Enrollment12000
Study TypeOBSERVATIONAL
ConditionsAbdominal 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

StatusRecruiting
PhaseN/A
SponsorRush University Medical Center
Enrollment148
Study TypeINTERVENTIONAL
ConditionsNeurologic 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

StatusRecruiting
PhaseN/A
SponsorAesculap AG
Enrollment200
Study TypeOBSERVATIONAL
ConditionsSpine 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

StatusRecruiting
PhaseN/A
SponsorHenry Ford Health System
Enrollment60
Study TypeINTERVENTIONAL
ConditionsNeoplasm 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

StatusRecruiting
PhaseN/A
SponsorClariance
Enrollment760
Study TypeOBSERVATIONAL
ConditionsSpine 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

StatusRecruiting
PhaseN/A
SponsorMedtronic Spinal and Biologics
Enrollment1000
Study TypeINTERVENTIONAL
ConditionsSpinal 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

StatusRecruiting
PhaseN/A
SponsorHospital for Special Surgery, New York
Enrollment48
Study TypeINTERVENTIONAL
ConditionsPatients 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

StatusRecruiting
PhaseN/A
SponsorEcole Polytechnique Fédérale de Lausanne
Enrollment3
Study TypeINTERVENTIONAL
ConditionsCervical 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

StatusRecruiting
PhaseN/A
SponsorUniversity Hospital, Bordeaux
Enrollment15000
Study TypeINTERVENTIONAL
ConditionsSpinal 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

StatusRecruiting
PhaseN/A
SponsorCopernicus Memorial Hospital
Enrollment226
Study TypeINTERVENTIONAL
ConditionsMetastatic 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

StatusRecruiting
PhaseN/A
SponsorAlabama Physical Therapy & Acupuncture
Enrollment120
Study TypeINTERVENTIONAL
ConditionsCervicogenic 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?

StatusRecruiting
PhaseN/A
SponsorIstituto Ortopedico Rizzoli
Enrollment200
Study TypeINTERVENTIONAL
ConditionsSpine 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

StatusRecruiting
PhaseN/A
SponsorNitin Agarwal
Enrollment100
Study TypeOBSERVATIONAL
ConditionsSpondylolisthesis, 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

StatusRecruiting
PhaseN/A
SponsorYale University
Enrollment100
Study TypeINTERVENTIONAL
ConditionsSpine 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

StatusRecruiting
PhaseN/A
SponsorWashington University School of Medicine
Enrollment160
Study TypeINTERVENTIONAL
ConditionsAcute 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

StatusRecruiting
PhasePhase 4
SponsorUniversity of Michigan
Enrollment160
Study TypeINTERVENTIONAL
ConditionsWound 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

StatusRecruiting
PhaseN/A
SponsorJason Carmel
Enrollment20
Study TypeINTERVENTIONAL
ConditionsSpinal 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

StatusActive, not recruiting
PhaseN/A
SponsorUniversity of Utah
Enrollment60
Study TypeOBSERVATIONAL
ConditionsPseudarthrosis 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

StatusActive, not recruiting
PhasePhase 2
SponsorM.D. Anderson Cancer Center
Enrollment60
Study TypeINTERVENTIONAL
ConditionsMalignant 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

StatusActive, not recruiting
PhasePhase 1
SponsorUniversity of Texas Rio Grande Valley
Enrollment30
Study TypeINTERVENTIONAL
ConditionsSpinal 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

StatusActive, not recruiting
PhaseN/A
SponsorNeo Medical SA
Enrollment150
Study TypeOBSERVATIONAL
ConditionsDegenerative 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)

StatusActive, not recruiting
PhaseN/A
SponsorRhode Island Hospital
Enrollment3
Study TypeINTERVENTIONAL
ConditionsSpinal 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

StatusActive, not recruiting
PhaseN/A
SponsorOrthofix Inc.
Enrollment2000
Study TypeOBSERVATIONAL
ConditionsSpinal 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

StatusActive, not recruiting
PhaseN/A
SponsorEcole Polytechnique Fédérale de Lausanne
Enrollment3
Study TypeINTERVENTIONAL
ConditionsSpinal 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

StatusActive, not recruiting
PhaseN/A
SponsorUniversity of South Florida
Enrollment42
Study TypeINTERVENTIONAL
ConditionsLow 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

StatusActive, not recruiting
PhaseN/A
SponsorSandra Jiménez-del-Barrio
Enrollment40
Study TypeINTERVENTIONAL
ConditionsSubacromial 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

StatusActive, not recruiting
PhaseN/A
SponsorCabinet d’ostéopathie Michel Boeuf
Enrollment50
Study TypeINTERVENTIONAL
ConditionsSpine 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

StatusNot yet recruiting
PhaseN/A
SponsorChang Gung Memorial Hospital
Enrollment104
Study TypeINTERVENTIONAL
ConditionsSpine 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.

StatusNot yet recruiting
PhaseN/A
SponsorThe University of Queensland
Enrollment120
Study TypeINTERVENTIONAL
ConditionsPersistent 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

StatusNot yet recruiting
PhasePhase 1
SponsorSport Injury Prevention Research Centre
Enrollment34
Study TypeINTERVENTIONAL
ConditionsMild 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

StatusNot yet recruiting
PhaseN/A
SponsorUniversity of Texas Southwestern Medical Center
Enrollment300
Study TypeOBSERVATIONAL
ConditionsPostoperative 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

StatusNot yet recruiting
PhaseN/A
SponsorMilwaukee VA Medical Center
Enrollment112
Study TypeINTERVENTIONAL
ConditionsSpine 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

StatusEnrolling by invitation
PhaseN/A
SponsorUniversity of California, San Francisco
Enrollment726
Study TypeOBSERVATIONAL
ConditionsSpinal 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

StatusEnrolling by invitation
PhaseN/A
SponsorNuVasive
Enrollment150
Study TypeOBSERVATIONAL
ConditionsDegenerative 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

StatusCompleted
PhasePhase 3
SponsorUniversity Hospital, Bordeaux
Enrollment50
Study TypeINTERVENTIONAL
ConditionsHyperalgesia
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

StatusCompleted
PhaseN/A
SponsorCentre Hospitalier Universitaire de Nīmes
Enrollment193
Study TypeOBSERVATIONAL
ConditionsQuality of Life; Spinal Injuries; Spinal Diseases

This study aims to:

  1. describe the monitoring of patients treated for spinal disorders.
  2. 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.
  3. obtain a cohort of …

NCT06873074 — A Retrospective Cohort Study About Surgical Efficacy for Lower Cervical Fractures in Ankylosing Spondylitis

StatusCompleted
PhaseN/A
SponsorZhou Fang
Enrollment162
Study TypeOBSERVATIONAL
ConditionsAnkylosing 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

StatusCompleted
PhaseN/A
SponsorNational Yang Ming Chiao Tung University
Enrollment37
Study TypeOBSERVATIONAL
ConditionsShoulder 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

StatusCompleted
PhaseN/A
SponsorMedical University of South Carolina
Enrollment20
Study TypeINTERVENTIONAL
ConditionsSpine 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

StatusCompleted
PhaseN/A
SponsorHacettepe University
Enrollment44
Study TypeOBSERVATIONAL
ConditionsBreast 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

StatusCompleted
PhaseN/A
SponsorUniversity Hospital, Montpellier
Enrollment50
Study TypeINTERVENTIONAL
ConditionsRugby; 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

StatusCompleted
PhaseN/A
SponsorRadiRad Co., Ltd.
Enrollment150
Study TypeOBSERVATIONAL
ConditionsSpinal 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

StatusCompleted
PhaseN/A
SponsorCairo University
Enrollment57
Study TypeOBSERVATIONAL
ConditionsFlexible 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

StatusCompleted
PhaseN/A
SponsorUniversity of Waterloo
Enrollment34
Study TypeINTERVENTIONAL
ConditionsOsteoporosis; 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

StatusCompleted
PhaseN/A
SponsorEge University
Enrollment72
Study TypeINTERVENTIONAL
ConditionsThorax 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

StatusCompleted
PhasePhase 4
SponsorFayoum University
Enrollment102
Study TypeINTERVENTIONAL
ConditionsAnalgesia
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

StatusCompleted
PhaseN/A
SponsorAnkara City Hospital Bilkent
Enrollment72
Study TypeINTERVENTIONAL
ConditionsLumbar 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

StatusTerminated
PhaseN/A
SponsorBarts & The London NHS Trust
Enrollment242
Study TypeINTERVENTIONAL
ConditionsSurgery; 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.

StatusTerminated
PhaseN/A
SponsorSilony Medical GmbH
Enrollment4
Study TypeOBSERVATIONAL
ConditionsDegenerative 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

StatusTerminated
PhaseN/A
SponsorUniversity of Pittsburgh
Enrollment2
Study TypeINTERVENTIONAL
ConditionsBrain 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…