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 Arm Injuries and Disorders from the ClinicalTrials.gov database.
Trial Summary
- Total studies: 50
- Recruiting: 19
- Active, not recruiting: 5
- Completed: 11
- Other: 15
Results are refreshed periodically and may not reflect the most current information available from ClinicalTrials.gov.
Recruiting Trials
NCT03253263 — A Clinical Efficacy and Safety Study of OHB-607 in Preventing Bronchopulmonary Dysplasia in Extremely Premature Infants
| Status | Recruiting |
| Phase | Phase 2 |
| Sponsor | OHB Neonatology Ltd. |
| Enrollment | 338 |
| Study Type | INTERVENTIONAL |
| Conditions | Bronchopulmonary Dysplasia; Chronic Lung Disease of Prematurity; Intraventricular Hemorrhage; Retinopathy of Prematurity (ROP) |
| Interventions |
The purpose of this study is to determine if an investigational drug can prevent Bronchopulmonary Dysplasia, reducing the burden of chronic lung disease in extremely premature infants, as compared to extremely premature infants receiving standard neonatal care alone.
NCT05163639 — Spinal Cord Associative Plasticity Study
| Status | Recruiting |
| Phase | Early Phase 1 |
| Sponsor | Columbia University |
| Enrollment | 92 |
| Study Type | INTERVENTIONAL |
| Conditions | Cervical Spinal Cord Injury; Tetraplegia/Tetraparesis; Cervical Myelopathy |
| Interventions | ; ; |
Spinal cord associative plasticity (SCAP) is a combined cortical and spinal electrical stimulation technique developed to induce recovery of arm and hand function in spinal cord injury.
The proposed study will advance understanding of SCAP, which is critical to its effective translation to human therapy. The purpose of the study is to:
- Determine whether signaling through the spinal cord to…
NCT05321017 — Wrist Extensor MEP Up-conditioning for Individuals With Incomplete Spinal Cord Injury
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Medical University of South Carolina |
| Enrollment | 5 |
| Study Type | INTERVENTIONAL |
| Conditions | Spinal Cord Injuries; Quadriplegia |
| Interventions |
The purpose of this study is to examine the relationship between common clinical assessments and measurements of the function of brain-spinal cord-muscle connections, and to examine the effects of training a brain-spinal cord-muscle response in individuals with incomplete spinal cord injury. A transcranial magnetic stimulator (TMS) is used for examining brain-to-muscle pathways. This stimulator…
NCT05142943 — Effectiveness of Virtual Bodily Illusion Intervention in Upper Limb Motor Function in People With Incomplete Spinal Cord Injury.
| Status | Recruiting |
| Phase | N/A |
| Sponsor | University of Valencia |
| Enrollment | 80 |
| Study Type | INTERVENTIONAL |
| Conditions | Incomplete Spinal Cord Injury; Spinal Cord Injury |
| Interventions | ; ; |
Previous studies have shown that the neuroplasticity of the residual corticospinal fibers, the motor cortex and the spinal neurons plays an important role in the spontaneous functional recovery of people with neurological or musculoskeletal pathology. However, it is also possible to stimulate the neuroplasticity mechanisms of these structures through techniques aimed at rehabilitating different…
NCT05131672 — Cast or Operation for Medial Epicondyle Fracture Treatment in Children
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Joseph Janicki |
| Enrollment | 334 |
| Study Type | INTERVENTIONAL |
| Conditions | Fracture Elbow |
| Interventions | ; |
This protocol describes a multicenter, prospective randomized and patient preference cohort superiority trial of medial epicondyle fracture treatments comparing functional outcomes between children treated with operative reduction and fixation or non-operative immobilization.
NCT05131685 — Distal Radius Interventions for Fracture Treatment
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Ann & Robert H Lurie Children’s Hospital of Chicago |
| Enrollment | 334 |
| Study Type | INTERVENTIONAL |
| Conditions | Fracture Distal Radius |
| Interventions | ; |
This protocol describes a multicenter, prospective randomized superiority trial with a patient preference cohort comparing functional outcomes between children treated with sedated reduction versus no formal reduction.
NCT06089915 — Effectiveness of Robot-assisted Upper-limb Exercise in Cervical SCI
| Status | Recruiting |
| Phase | N/A |
| Sponsor | University Rehabilitation Institute, Republic of Slovenia |
| Enrollment | 30 |
| Study Type | INTERVENTIONAL |
| Conditions | Cervical Vertebrae Injury |
| Interventions | ; |
The aim of the project is to test the effectiveness of robot-assisted upper-limb exercise in persons after cervical spinal cord injury. In a randomised controlled two-arm trial, the effect of adding two types of robot-assisted upper-limb exercise to standard occupational therapy will be tested. Three primary and two secondary outcomes will be assessed using well-established measures.
NCT06616025 — This Study Will Evaluate the Effectiveness of NTX-001, a Surgical Nerve Repair Product When Used in People With Upper Extremity Nerve Lacerations.
| Status | Recruiting |
| Phase | Phase 3 |
| Sponsor | Neuraptive Therapeutics Inc. |
| Enrollment | 98 |
| Study Type | INTERVENTIONAL |
| Conditions | Peripheral Nerve Injury Upper Limb; Peripheral Nerve Injury (PNI) |
| Interventions |
NTX-001 is a single use surgical product intended for use in conjunction with standard suture neurorrhaphy of severed nerves in patients between 18 and 80.
NCT06869343 — Early Versus Delayed Rehabilitation After Reverse Total Shoulder Arthroplasty for Proximal Humerus Fracture
| Status | Recruiting |
| Phase | N/A |
| Sponsor | University of Virginia |
| Enrollment | 10 |
| Study Type | INTERVENTIONAL |
| Conditions | Orthopedic Disorder; Humerus Fracture; Shoulder Arthroplasty; Reverse Shoulder Replacement |
| Interventions |
Proximal humerus fractures can be a debilitating injury in the elderly, impacting the ability to function independently or complete activities of daily living due to pain and restricted shoulder motion. Evidence has shown that reverse total shoulder arthroplasty (rTSA) is an effective option to improve pain and function for patients with acute displaced proximal humerus fractures. Given that pa…
NCT07178288 — Assessment of Pressure Pain Threshold (PPT) and Conditioned Pain Modulation (CPM) After Effect in Patients With and Without Tennis Elbow (TE)
| Status | Recruiting |
| Phase | N/A |
| Sponsor | The Hashemite University |
| Enrollment | 38 |
| Study Type | INTERVENTIONAL |
| Conditions | Tennis Elbow; Health Adult Subjects; Lateral Elbow Tendinopathy (Tennis Elbow); Pressure Pain Threshold (PPT); Conditioned Pain Modulation (CPM) |
| Interventions |
This study at Hashemite University looks at how people with and without tennis elbow (AKA lateral elbow tendinopathy) feel pressure pain and how their bodies briefly “turn down” pain after a cold stimulus. Participants complete brief questionnaires (basic demographics without names, a tennis-elbow symptom form, and a physical-activity form) and then have their pressure-pain threshold (PPT) test…
NCT07153536 — Spinal Cord Stimulation Combined With Physical Therapy in Post-Stroke Upper-Limb Motor Hemiparesis
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Marco Capogrosso |
| Enrollment | 20 |
| Study Type | INTERVENTIONAL |
| Conditions | Stroke; Spinal Cord Injuries and Disorders; Hemiparesis After Stroke |
| Interventions | ; |
This study plans to use systems that have been developed by Medtronic to investigate the use of cervical spinal cord stimulation to treat adults with upper limb hemiparesis resulting from a stroke. The spinal cord stimulation (SCS) will be combined with physical training to improve arm and hand motor control. The study is divided into three phases. In the first phase, after baseline assessments…
NCT07633769 — Virtual Reality-based Rehabilitation for Traumatic Hand and Wrist Injuries
| Status | Recruiting |
| Phase | N/A |
| Sponsor | University of Malaga |
| Enrollment | 40 |
| Study Type | INTERVENTIONAL |
| Conditions | Wrist Injury; Hand and Upper Limb Trauma; Hand and Forearm Trauma; Muskuloskeletal Diseases |
| Interventions | ; |
This randomized controlled trial aims to evaluate the effectiveness of immersive virtual reality (VR)-based Action Observation Therapy (AOT) as an adjunct to conventional rehabilitation in patients with traumatic wrist and hand injuries. Participants will receive standard rehabilitation treatment, and the intervention group will additionally undergo a six-week VR program involving observation a…
NCT07143019 — The Use of p48/64 MW HPC Flow Modulation Device in the Treatment of Wide-necked Intracranial Aneurysms
| Status | Recruiting |
| Phase | N/A |
| Sponsor | phenox Inc. |
| Enrollment | 214 |
| Study Type | INTERVENTIONAL |
| Conditions | Hemorrhagic Stroke; Aneurysm, Intracranial; Saccular Aneurysm; Fusiform Aneurysm; Brain Aneurysm |
| Interventions |
To determine safety and effectiveness of the p48 MW HPC and p64 MW HPC Flow Modulation Device in the treatment of wide-necked intracranial aneurysms.
NCT07564713 — Comparison of Extracorporeal Shock Wave Therapy and Low-Level Laser Therapy in Patients With Lateral Epicondylitis
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Hitit University |
| Enrollment | 50 |
| Study Type | INTERVENTIONAL |
| Conditions | Lateral Epicondylitis (Tennis Elbow) |
| Interventions | ; |
Background:
Lateral epicondylitis is a common musculoskeletal condition characterized by pain and functional impairment of the elbow, often associated with degenerative changes in the common extensor tendon. Extracorporeal shock wave therapy (ESWT) and low-level laser therapy (LLLT) are widely used noninvasive treatment modalities; however, comparative evidence regarding their clinical and str…
NCT07634224 — Evaluation of the Effectiveness of Capacitive and Resistive Energy Transfer Therapy for Lateral Epicondylitis
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Gaziantep City Hospital |
| Enrollment | 62 |
| Study Type | INTERVENTIONAL |
| Conditions | Lateral Epicondylitis; Capacitive and Resistive Electric Transfer Therapy; Exercise |
| Interventions | ; |
This prospective, randomized, double-blind, sham-controlled clinical trial aims to evaluate the efficacy of Capacitive and Resistive Energy Transfer (TECAR) therapy in patients with lateral epicondylitis. Participants will be randomly assigned to either a TECAR plus exercise group or a sham TECAR plus exercise group.
Both groups will receive a standardized home exercise program including elbow…
NCT07538323 — Wrist Injury Strengthening Exercise (WISE) Versus Usual Care Advice for Improving Pain and Function
| Status | Recruiting |
| Phase | N/A |
| Sponsor | University of Aarhus |
| Enrollment | 588 |
| Study Type | INTERVENTIONAL |
| Conditions | Distal Radius Fracture; Colles Fracture; Wrist Fracture; Wrist Fractures; Fracture Arm |
| Interventions | ; |
The goal of this clinical trial is to find out whether a therapist-guided exercise program helps people aged 50 and older recover better, in terms of pain and function, after a wrist fracture, compared to the usual care advice they would normally receive. The main question it aims to answer is:
• Will participants who receive a therapist-supervised exercise program have better improvement in p…
NCT07657182 — A Prospective, Randomized, Assessor-Blinded, Multicenter Study Comparing Avance Nerve Graft and Autograft for Functional Recovery Following Mixed and Motor Peripheral Nerve Reconstruction
| Status | Recruiting |
| Phase | Phase 4 |
| Sponsor | Axogen Corporation |
| Enrollment | 178 |
| Study Type | INTERVENTIONAL |
| Conditions | Peripheral Nerve Injury; Peripheral Nerve Discontinuity; Mixed Peripheral Nerve Injury; Motor Peripheral Nerve Injury; Upper Extremity Nerve Injury |
| Interventions | ; |
This is a multicenter, 1:1 randomized, prospective, comparative study in participants requiring reconstruction of a mixed or motor nerve in the upper extremity. This study will consist of a screening visit, an operative visit, and 9 post-operative follow-up visits at Week 4, and Months 3, 6, 9, 12, 15, 18, 21, and 24.
NCT06998134 — Toward Ubiquitous Lower Limb Exoskeleton Use in Children and Young Adults
| Status | Recruiting |
| Phase | N/A |
| Sponsor | National Institutes of Health Clinical Center (CC) |
| Enrollment | 23 |
| Study Type | OBSERVATIONAL |
| Conditions | Muscle Weakness; Problems Moving Their Arms and Legs |
| Interventions |
People with cerebral palsy (CP), muscular dystrophy (MD), spina bifida, or spinal cord injury often have muscle weakness, and problems moving their arms and legs. The NIH designed a new brace device, called an exoskeleton, that is worn on the legs and helps people walk. This study is investigating new ways the exoskeleton can be used in multiple settings while performing different walking or mo…
NCT07552766 — A Clinical Trial on the Use of Lidocaine Infusion During Surgery for Pediatric Upper Extremity Fractures and Its Impact on Total Perioperative Opioid Requirements
| Status | Recruiting |
| Phase | Phase 4 |
| Sponsor | Nemours Children’s Clinic |
| Enrollment | 90 |
| Study Type | INTERVENTIONAL |
| Conditions | Fracture Arm; Fracture Closed of Lower End of Forearm, Unspecified; Fracture Elbow; Fracture Fixation; Fracture Fixation, Internal |
| Interventions | ; |
This study is a prospective, randomized, double-blind clinical trial evaluating whether intraoperative intravenous lidocaine infusion (IVLI) reduces opioid requirements and improves postoperative pain control in children undergoing surgical fixation of upper extremity long bone fractures under general anesthesia. Ninety pediatric patients, ages 3-18 will be enrolled and randomized 1:1 to receiv…
Active, Not Recruiting
NCT03992404 — Study to Compare the Efficacy and Safety of NT 201 (Botulinum Toxin) With Placebo for the Treatment of Lower Limb Spasticity Caused by Stroke or Traumatic Brain Injury
| Status | Active, not recruiting |
| Phase | Phase 3 |
| Sponsor | Merz Pharmaceuticals GmbH |
| Enrollment | 603 |
| Study Type | INTERVENTIONAL |
| Conditions | Lower Limb or Combined Lower Limb and Upper Limb Spasticity Due to Stroke or Traumatic Brain Injury |
| Interventions | ; |
The purpose of this study is to determine whether a single treatment with administration of 400 Units NT 201 (botulinum toxin) is superior to placebo (no medicine) for the treatment of lower limb spasticity caused by stroke or traumatic brain injury (Main Period). Participants will be assigned to the treatment groups by chance and neither the participants nor the research staff who interact wit…
NCT04023591 — Nerve Transfer After Spinal Cord Injury- Multi-center
| Status | Active, not recruiting |
| Phase | N/A |
| Sponsor | Washington University School of Medicine |
| Enrollment | 70 |
| Study Type | OBSERVATIONAL |
| Conditions | Tetraplegia; Spinal Cord Injuries; Quadriplegia Flaccid |
| Interventions |
Current treatment strategies of acute cervical spinal cord injuries remain limited. Treatment options that provide meaningful improvements in patient quality of like and long-term functional independence will provide a significant public health impact. Specific aim: Measure the efficacy of nerve transfer surgery in the treatment of patients with complete spinal cord injuries with no hand functi…
NCT04928261 — Evaluating 6-months of HER2-targeted Therapy in Patients With HER2 Positive Early-stage Breast Cancer That Achieve a Pathological Complete Response to Neoadjuvant Systemic Therapy
| Status | Active, not recruiting |
| Phase | Phase 4 |
| Sponsor | Ottawa Hospital Research Institute |
| Enrollment | 52 |
| Study Type | INTERVENTIONAL |
| Conditions | Breast Cancer |
| Interventions |
The activity of trastuzumab in early-stage, HER2-positive breast cancer, has been demonstrated in many studies, with meta-analyses showing that in combination with a variety of chemotherapy backbones, trastuzumab reduces the risk of recurrence by nearly half, and death by a third. However, treatment with trastuzumab can result in cardiotoxicity, including heart failure, as well as the significa…
NCT05325242 — Elbow Artery Embolization for Tennis Elbow
| Status | Active, not recruiting |
| Phase | N/A |
| Sponsor | Siddharth Padia, MD |
| Enrollment | 13 |
| Study Type | INTERVENTIONAL |
| Conditions | Lateral Epicondylitis, Unspecified Elbow |
| Interventions |
The purpose of this clinical research study is to examine whether embolization treatment of an elbow artery is a safe and effective way to treat elbow pain, specifically pain from tennis elbow. Embozene is a medical device made by Varian marketed in the United States for the treatment of hypervascular tumors and arteriovenous malformations. It consists of thousands of microscopic spheres that a…
NCT07645768 — Is Anterior Reversed Proximal Humeral Locking Plate System (PHILOS) a Safe Alternative to Conventional Posterior Double Plating in Extra-Articular Distal Shaft Humeral Fractures
| Status | Active, not recruiting |
| Phase | N/A |
| Sponsor | Cairo University |
| Enrollment | 68 |
| Study Type | INTERVENTIONAL |
| Conditions | Humeral Fracture |
| Interventions | ; |
Extra-articular distal-third humeral shaft fractures are difficult to treat because stable fixation must be achieved while minimizing soft-tissue injury and the risk of nerve damage. Posterior double plating is a commonly used technique but requires extensive surgical exposure and routine handling of the radial and ulnar nerves. Anterior reversed proximal humeral locking plate system (PHILOS) f…
Not Yet Recruiting
NCT07626983 — Botulinum Toxin Type A Versus Local Anesthetic Injection for Chronic Neuroma Pain After Combat-Related Amputation
| Status | Not yet recruiting |
| Phase | N/A |
| Sponsor | Ukrainian Society of Regional Anesthesia and Pain Therapy |
| Enrollment | 100 |
| Study Type | INTERVENTIONAL |
| Conditions | Chronic Pain Due to Injury; Neuroma of Lower Limb; Neural Injury; Neuroma of Upper Limb; Combat Related Symptoms |
| Interventions | ; |
Patients with combat-related amputations frequently experience persistent neuroma pain that may interfere with rehabilitation, prosthesis use, sleep, mobility, and quality of life. Current treatment options often provide only temporary relief. This study aims to compare two ultrasound-guided injection approaches for chronic neuroma pain after combat-related amputation: botulinum toxin type A an…
NCT07632521 — CLAP : Compare the Quality of 3D Modeling of the Wrist Based on the Cone Beam to the Gold Standard
| Status | Not yet recruiting |
| Phase | N/A |
| Sponsor | Centre Hospitalier Universitaire de Besancon |
| Enrollment | 6 |
| Study Type | INTERVENTIONAL |
| Conditions | Wrist Injuries; Ligament Injury |
| Interventions | ; |
Recent advances in personalized 3D modeling make it possible to consider personalized hand modeling based on cone-beam CT. The goal is to develop a personalized 3D modeling tool for use in routine clinical practice that reduces both the radiation dose to which patients are currently exposed during CT scans and the time required to process CT data (segmentation). the main, objective of the study…
NCT07648849 — Arthroscopic Versus Open Management of Lateral Epicondylitis Elbow (Randomized Control Trial)
| Status | Not yet recruiting |
| Phase | N/A |
| Sponsor | Assiut University |
| Enrollment | 50 |
| Study Type | INTERVENTIONAL |
| Conditions | Tennis Elbow |
| Interventions | ; |
Arthroscopic Versus Open management of lateral epicondylitis elbow (Randomized Control Trial)
NCT07682207 — Accelerated iTBS for PTSD and Depression
| Status | Not yet recruiting |
| Phase | N/A |
| Sponsor | Lawson Research Institute of St. Joseph’s |
| Enrollment | 16 |
| Study Type | INTERVENTIONAL |
| Conditions | Post Traumatic Stress Disorder PTSD; Major Depressive Disorder (MDD) |
| Interventions |
The goal of this pilot clinical trial is to learn if a faster brain stimulation schedule is practical, safe, tolerable, and acceptable. This study looks at accelerated intermittent theta burst stimulation, or accelerated iTBS. This is a non-invasive type of magnetic brain stimulation. This study is for adults with post-traumatic stress disorder (PTSD) and major depressive disorder (MDD).
The m…
NCT07654621 — Combined Manual Therapy and Percutaneous Neuromodulation for Moderate Carpal Tunnel Syndrome
| Status | Not yet recruiting |
| Phase | N/A |
| Sponsor | Universidad Europea de Valencia |
| Enrollment | 150 |
| Study Type | INTERVENTIONAL |
| Conditions | Carpal Tunnel Syndrome |
| Interventions | ; |
Carpal tunnel syndrome (CTS) is the most common peripheral entrapment neuropathy and can cause pain, numbness, tingling, and functional impairment of the hand. Although surgical decompression is considered an effective treatment for moderate CTS, there is increasing interest in conservative therapeutic strategies that may improve symptoms and function while avoiding surgery.
The aim of this mu…
NCT07688096 — Regenerative Medicine for Joint Hypermobility and Instability
| Status | Not yet recruiting |
| Phase | Phase 1 / Phase 2 |
| Sponsor | Manhattan Pain Medicine, PLLC |
| Enrollment | 100 |
| Study Type | INTERVENTIONAL |
| Conditions | Ehlers-Danlos Syndrome Hypermobility Type (hEDS); Ehlers-Danlos Syndrome (EDS); Joint Hypermobility; Joint Instability; Hypermobility Spectrum Disorder |
| Interventions | ; ; |
This clinical trial is designed to evaluate whether a stepwise injection-based treatment approach can reduce pain and improve function in adults with joint hypermobility, connective tissue laxity, and joint instability.
Joint hypermobility occurs when joints move beyond their normal range, often because of looser connective tissue. For some patients, this can contribute to chronic pain, recurr…
NCT07668531 — Kinesiophobia and Functional Outcomes in Distal Radius Fractures
| Status | Not yet recruiting |
| Phase | N/A |
| Sponsor | Ebru Aloğlu Çiftçi |
| Enrollment | 100 |
| Study Type | INTERVENTIONAL |
| Conditions | Distal Radius Fracture |
| Interventions |
Distal radius fractures are among the most common fractures in adults and are frequently treated with closed reduction and cast immobilization. Although fracture healing is generally successful, some patients may develop fear of movement (kinesiophobia) after cast removal because of pain, reinjury concerns, or reduced confidence in using the injured wrist.
The purpose of this study is to evalu…
NCT07240649 — Emerging Indications for Hyperbaric Oxygen Treatment
| Status | Not yet recruiting |
| Phase | Phase 4 |
| Sponsor | Jay C. Buckey Jr. |
| Enrollment | 100 |
| Study Type | INTERVENTIONAL |
| Conditions | Post-COVID-19 Condition; Ulcerative Colitis; Crohn Disease; Calciphylaxis; Frostbite |
| Interventions | ; |
This study will evaluate the effectiveness of hyperbaric oxygen therapy (HBOT) on treating emerging indications (i.e., conditions that have shown to potentially benefit from HBOT) using the Multicenter Registry for Hyperbaric Oxygen Treatment. The study team aims to collect ongoing data on how well HBOT treats these emerging indications, and to add these data to the growing HBO Registry. The re…
NCT07361627 — Upper Limb Rehabilitation Using Non-invasive Spinal Cord Stimulation
| Status | Not yet recruiting |
| Phase | N/A |
| Sponsor | Centre for Interdisciplinary Research in Rehabilitation of Greater Montreal |
| Enrollment | 40 |
| Study Type | INTERVENTIONAL |
| Conditions | Spinal Cord Injury Cervical; Spinal Cord Injury, Acute; Spinal Cord Injury (Quadraplegia) |
| Interventions | ; |
The goal of this RCT study is to evaluate if combining activity-based therapy (ABT) with transcutaneous spinal cord stimulation (tSCS) can improve recovery of arm and hand movement in people with cervical spinal cord injury (SCI). As secondary aims, the study will also investigate at how this combination approach affects the cortical changes in the somatosensory and motor areas of the brain, as…
Enrolling by Invitation
NCT07653165 — Use of Hydroprep Wound Therapy With Motion Negative Pressure Therapy for Treatment of Chronic Lower Extremity Wounds
| Status | Enrolling by invitation |
| Phase | N/A |
| Sponsor | West Boca Center for Wound Healing |
| Enrollment | 50 |
| Study Type | INTERVENTIONAL |
| Conditions | Chronic Lower Leg Ulcer; Diabetic Lower Extremity Ulcers; Pressure Injuries; Traumatic Wounds and Injuries; Surgical Wounds |
| Interventions |
Use of a motorized waterjet to debride wounds to improve healing outcomes.
NCT07577960 — Effect of Pulmonary Rehabilitation on Respiratory Parameters in Upper Extremity Burns
| Status | Enrolling by invitation |
| Phase | N/A |
| Sponsor | Fenerbahce University |
| Enrollment | 64 |
| Study Type | INTERVENTIONAL |
| Conditions | Burn Injury; Pulmonary Rehabilitation |
| Interventions | ; |
This study will evaluate the effects of a pulmonary rehabilitation program on breathing function, respiratory muscle activity, respiratory muscle thickness, and functional capacity in adults with upper extremity burns. Participants will be randomly assigned to either a pulmonary rehabilitation group or a control group. The pulmonary rehabilitation group will receive respiratory muscle training …
Completed Trials
NCT07627932 — Comparison of the Effectiveness of Blood Flow Restriction Exercise and Eccentric Exercise in Lateral Epicondylitis
| Status | Completed |
| Phase | N/A |
| Sponsor | Manisa Celal Bayar University |
| Enrollment | 27 |
| Study Type | INTERVENTIONAL |
| Conditions | Lateral Epicondylitis |
| Interventions | ; ; |
This study compared three different treatment approaches for lateral epicondylitis (tennis elbow), a common condition that causes pain on the outside of the elbow.Twenty-seven patients diagnosed with lateral epicondylitis were randomly assigned to one of three treatment groups for 6 weeks:Group 1 - Blood Flow Restriction Exercise (BFRE): Patients performed wrist strengthening exercises using li…
NCT07661615 — Arthroscopic or Open Evaluation of Posterolateral Instability Associated With Lateral Epicondylitis
| Status | Completed |
| Phase | N/A |
| Sponsor | Ramsay Générale de Santé |
| Enrollment | 30 |
| Study Type | OBSERVATIONAL |
| Conditions | Elbow Arthroscopy Surgery; Elbow Injury; Epicondylitis of the Elbow; Epicondylitis, Lateral |
| Interventions | ; |
The elbow is a complex joint made up of three bones, three joints, and three ligaments. Repeated microtraumas can lead to ligament injuries and instability, tendon damage, or degenerative processes affecting the bones, cartilage, and bursae. As a result, elbow pain is not uncommon, and diagnosing the underlying problem is not always easy. One reason for this is the complex anatomy packed into a…
NCT05328934 — SoftHand Comparison Study
| Status | Completed |
| Phase | N/A |
| Sponsor | Mayo Clinic |
| Enrollment | 36 |
| Study Type | INTERVENTIONAL |
| Conditions | Upper Extremity Injury; Upper Extremity Deformities, Congenital; Amputation, Traumatic; Amputation, Congenital |
| Interventions | ; |
A trial to compare the performance of the SoftHand Pro (SHP) and Ossur i-Limb in people with transradial limb loss over an 8-week period.
NCT07625787 — Efficacy and Safety of Hematoma Block Versus Brachial Plexus Block for Closed Reduction of Extra-Articular Distal Radius Fracture: A Prospective Study
| Status | Completed |
| Phase | N/A |
| Sponsor | Kathmandu University School of Medical Sciences |
| Enrollment | 90 |
| Study Type | INTERVENTIONAL |
| Conditions | Distal Radius Fracture; Brachial Plexus Block; Hematoma Block |
| Interventions | ; |
Distal radius fractures are one of the most common types of fractures, affecting mostly youngsters and the elderly. Safety, ease of use, affordability, and effectiveness all play a role in analgesia during reduction. This study’s goal is to assess how well the Hematoma Block (HB) reduces distal forearm fractures in a developing nation like Nepal. At a tertiary care hospital, a randomized compar…
NCT07637838 — Characterizing the Effects of Platelet-Rich Fibrin (PRF) as a Palatal Wound Dressing on Quality of Life and Sleep Following Mucogingival Surgery. Study Was Conducted at the Air Force Post Graduate Dental School. All HIPPA Consents and Research Informed Consents Are Located at JBSA-Lackland.
| Status | Completed |
| Phase | N/A |
| Sponsor | 59th Medical Wing |
| Enrollment | 78 |
| Study Type | INTERVENTIONAL |
| Conditions | Palatal Donor Site Wound Healing; Platelet Rich Fibrin; Sleep Quality; Pain; Analgesic Consumption |
| Interventions | ; |
The goal of this clinical trial (2-arm) is to determine if the application of platelet rich fibrin (PRF) to palatal donor sites influence patients quality of life, sleep efficiency, and healing following mucogingival surgery. All patients were enrolled in the Air Force Post Graduate Dental School periodontics program and each patient required mucogingival surgery. The main question[s] it aims…
NCT06211296 — The ShortCut™ Continued Access Study Protocol
| Status | Completed |
| Phase | N/A |
| Sponsor | Pi-cardia |
| Enrollment | 8 |
| Study Type | INTERVENTIONAL |
| Conditions | Valve-in-valve Procedures; Aortic Stenosis; Coronary; Obstruction |
| Interventions |
A Prospective, Multicenter, Non-Randomized, Single-Arm, Open-Label Continued Access Study of the ShortCut™ device (The ShortCut™ CAS).
NCT07638488 — Trigger Point Extracorporeal Shock Wave Therapy in Patients With Lateral Epicondylitis
| Status | Completed |
| Phase | N/A |
| Sponsor | Gazi University |
| Enrollment | 52 |
| Study Type | INTERVENTIONAL |
| Conditions | Lateral Epicondylitis (Tennis Elbow) |
| Interventions | ; |
This randomized controlled study evaluates the effect of extracorporeal shock wave therapy applied to the extensor carpi radialis brevis trigger point in patients with lateral epicondylitis. Participants receive active extracorporeal shock wave therapy to the lateral epicondyle region. In addition, one group receives active extracorporeal shock wave therapy to the extensor carpi radialis brevis…
NCT07643740 — COMPARATIVE EFFECTS OF DRY NEEDLING AND NEURAL MOBILIZATION ON PAIN, STRENGTH AND RANGE OF MOTION IN PATIENTS WITH GOLFER’S ELBOW
| Status | Completed |
| Phase | N/A |
| Sponsor | Green International University |
| Enrollment | 29 |
| Study Type | INTERVENTIONAL |
| Conditions | Golfer’s Elbow; Medial Epicondylitis |
| Interventions | ; |
This randomized clinical trial aims to compare the effectiveness of Dry Needling and Neural Mobilization in patients diagnosed with Golfer’s Elbow (Medial Epicondylitis). The study will evaluate the effects of both interventions on pain intensity, grip strength, and range of motion. Participants will be randomly allocated to either the Dry Needling group or the Neural Mobilization group and tre…
NCT06912217 — Comparison of the Effects of Robotic Rehabilitation, Functional Electrical Stimulation and Occupational Therapy on Upper Extremity and Hand Functions in Tetraplegic Patients With Spinal Cord Injury
| Status | Completed |
| Phase | N/A |
| Sponsor | Ankara City Hospital Bilkent |
| Enrollment | 30 |
| Study Type | INTERVENTIONAL |
| Conditions | Tetraplegia/Tetraparesis |
| Interventions | ; ; |
2. Purpose and Significance of the Study (Primary and Secondary Objectives, if any) Spinal cord injury (SCI) is a clinical condition characterized by partial or total loss of motor, sensory, and autonomic functions below the level of the lesion, depending on the severity and level of the injury, which may be caused by traumatic or non-traumatic factors.
Globally, the incidence of SCI is estim…
NCT07667491 — Effects of 8 Weeks of Two Exercise Programs on Risk Factors Associated With Epicondylitis in Amateur Padel Players
| Status | Completed |
| Phase | N/A |
| Sponsor | School of Allied Health Sciences of Porto (ESTSP) - Polytechnic Institute of Porto (IPP) |
| Enrollment | 45 |
| Study Type | INTERVENTIONAL |
| Conditions | Lateral Epicondylitis; Prevention |
| Interventions |
Background: The physical demands of padel can increase the risk of injuries, particularly lateral epicondylitis in the elbow. Key risk factors include deficits in forearm muscle strength and rotator cuff weakness. Prevention programs focus on forearm strengthening, with no studies on rotator cuff strength. This study aims to compare two exercise programs designed to reduce risk factors for late…
NCT07424794 — Mobilization With Movement Verses Cyriax Techniques Among Athletes With Lateral Epicondylitis
| Status | Completed |
| Phase | N/A |
| Sponsor | Mohammad Affan |
| Enrollment | 56 |
| Study Type | INTERVENTIONAL |
| Conditions | Lateral Epicondylitis |
| Interventions | ; |
This randomized controlled trial aims to compare the effectiveness of Mobilization with Movement (MWM) and Cyriax techniques in athletes diagnosed with lateral epicondylitis (tennis elbow). Lateral epicondylitis commonly causes pain, reduced grip strength, and impaired proprioception, particularly in racquet and throwing sports players. A total of 56 participants aged 25-40 years with symptoms …
Other (Withdrawn)
NCT00909272 — Ultrasound Guided Diagnostic Lumbar Medial Branch Blocks
| Status | Withdrawn |
| Phase | N/A |
| Sponsor | McMaster University |
| Enrollment | N/A |
| Study Type | OBSERVATIONAL |
| Conditions | Back Pain |
| Interventions | ; |
Can an ultrasound machine be used to perform a diagnostic lumbar medial branch block?
Other (Suspended)
NCT05237869 — Blood Flow Restriction & Tennis Elbow Rehab
| Status | Suspended |
| Phase | N/A |
| Sponsor | Julie Nuelle |
| Enrollment | 250 |
| Study Type | INTERVENTIONAL |
| Conditions | Lateral Epicondylitis |
| Interventions | ; |
Lateral epicondylitis (LE), often referred to as “tennis elbow” is a common and debilitating overuse injury affecting 1-3% of adults annually. LE is most often defined as a syndrome of pain near the area of the lateral epicondyle of the elbow commonly effecting the origin of the extensor carpi radialis brevis with associated weakness; it most commonly effects the dominant arm. The best treatmen…
NCT05948540 — Department of Defense PTSD Adaptive Platform Trial - Intervention C - Daridorexant
| Status | Suspended |
| Phase | Phase 2 |
| Sponsor | Global Coalition for Adaptive Research |
| Enrollment | 200 |
| Study Type | INTERVENTIONAL |
| Conditions | Post Traumatic Stress Disorder |
| Interventions | ; |
This is a Phase 2 randomized, double-blinded, placebo-controlled study that will evaluate multiple potential pharmacotherapeutic interventions for PTSD utilizing an adaptive platform trial design.
Intervention C - Daridorexant will assess the safety and efficacy of daridorexant in participants with PTSD.
Please see NCT05422612 for information on the S-21-02 Master Protocol.
NCT05422612 — Department of Defense PTSD Adaptive Platform Trial - Master Protocol
| Status | Suspended |
| Phase | Phase 2 |
| Sponsor | Global Coalition for Adaptive Research |
| Enrollment | 800 |
| Study Type | INTERVENTIONAL |
| Conditions | Post Traumatic Stress Disorder |
| Interventions | ; ; |
This is a Phase 2 randomized, double-blinded, placebo-controlled study that will evaluate multiple potential pharmacotherapeutic interventions for PTSD utilizing an adaptive platform trial design. Participants are randomized among the available cohorts in the study and the resulting randomization enables sharing/pooling of control participants, where all interventions may be compared to a commo…