[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"wrist-injuries\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:wrist-injuries":28},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,6,0,[8,45,70,116,137,166],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":15,"eligibilityCriteria":16,"healthyVolunteers":17,"sex":18,"minAge":19,"maxAge":20,"enrollmentInfo":21,"targetDuration":4,"studyType":23,"phases":24,"briefSummary":26,"conditions":27,"keywords":30,"overallStatus":33,"whyStopped":4,"lastUpdateSubmitDate":34,"lastUpdatePostDateStruct":35,"startDateStruct":38,"completionDateStruct":40,"leadSponsor":42,"locationsCount":4},"100643286","clap--compare-the-quality-of-3d-modeling-of-the-wrist-based-on-the-cone-beam-to-the-gold-standard-100643286",false,"NCT07632521","CLAP : Compare the Quality of 3D Modeling of the Wrist Based on the Cone Beam to the Gold Standard","CLAP: Single Center Prospective Study to Compare the Quality of 3D Modeling of the Wrist Based on the Cone Beam to the Gold Standard of CT SCAN in 6 Healthy Volunteers.","CLAP","Inclusion Criteria:\n\n* no clinical symptoms suggestive of a wrist ligament injury (e.g., pain, instability)\n* no contraindications to undergoing a CBCT scan (e.g., pregnancy, history of hypersensitivity to radiation).\n* Enrolled in or eligible for a French social security plan.\n* Signing of an informed consent form indicating that the subject understands the purpose and procedures required by the study and agrees to participate in the study and comply with the requirements and restrictions inherent to this study\n\nExclusion Criteria:\n\n* Pregnant women and breastfeeding mothers\n* Persons deprived of their liberty by a judicial or administrative decision; persons undergoing involuntary psychiatric treatment; persons admitted to a health or social care facility for purposes other than research\n* Adults subject to a legal protection measure (judicial protection, guardianship, or conservatorship) or who are unable to give consent",true,"ALL","18 Years","65 Years",{"count":5,"type":22},"ESTIMATED","INTERVENTIONAL",[25],"NA","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 is to compare the quality of 3D hand modeling based on cone-beam CT with the gold standard of computed tomography.\n\nThis prospective, single-center, interventional study will include 6 healthy volunteers.",[28,29],"Wrist Injuries","Ligament Injury",[31,32],"CT scan","cone-beam scan","NOT_YET_RECRUITING","2026-06-02",{"date":36,"type":37},"2026-06-08","ACTUAL",{"date":39,"type":22},"2026-06-01",{"date":41,"type":22},"2026-10-30",{"name":43,"class":44},"Centre Hospitalier Universitaire de Besancon","OTHER",{"id":46,"slug":47,"hasResults":11,"nctId":48,"briefTitle":49,"officialTitle":50,"acronym":4,"eligibilityCriteria":51,"healthyVolunteers":11,"sex":18,"minAge":19,"maxAge":4,"enrollmentInfo":52,"targetDuration":4,"studyType":23,"phases":54,"briefSummary":55,"conditions":56,"keywords":4,"overallStatus":59,"whyStopped":4,"lastUpdateSubmitDate":60,"lastUpdatePostDateStruct":61,"startDateStruct":63,"completionDateStruct":65,"leadSponsor":67,"locationsCount":69},"100635462","splinted-wrist-study-100635462","NCT07553000","Splinted Wrist Study","The Additional Pain Relieving Benefit of Using a Splint in Suspected Wrist Fractures in Adult Patients at an Emergency Department - a Randomized Controlled Trial.","Inclusion Criteria:\n\n* NRS 5-10\n* Suspected distal fracture of radius\n\nExclusion Criteria:\n\n* No X-ray veriefied fracture.",{"count":53,"type":22},120,[25],"Randomized clinical trial comparing SAM aluminium splint vs pain relief as usual in patients seeking emergency department care for suspected wrist fractures.",[28,57,58],"Wrist Fracture","Pain, Acute","RECRUITING","2026-04-24",{"date":62,"type":37},"2026-04-27",{"date":64,"type":37},"2022-12-14",{"date":66,"type":22},"2027-12-30",{"name":68,"class":44},"Region Skane",1,{"id":71,"slug":72,"hasResults":11,"nctId":73,"briefTitle":74,"officialTitle":75,"acronym":76,"eligibilityCriteria":77,"healthyVolunteers":11,"sex":18,"minAge":19,"maxAge":4,"enrollmentInfo":78,"targetDuration":4,"studyType":80,"phases":4,"briefSummary":81,"conditions":82,"keywords":101,"overallStatus":33,"whyStopped":4,"lastUpdateSubmitDate":107,"lastUpdatePostDateStruct":108,"startDateStruct":110,"completionDateStruct":112,"leadSponsor":114,"locationsCount":69},"100633082","early-functional-response-as-a-predictor-of-clinical-outcomes-in-hand-rehabilitation-a-prospective-feasibility-study-using-a-digital-monitoring-system-100633082","NCT07522060","Early Functional Response as a Predictor of Clinical Outcomes in Hand Rehabilitation: A Prospective Feasibility Study Using a Digital Monitoring System","Early Functional Response as a Predictor of Clinical Outcomes in Hand Rehabilitation: A Prospective Feasibility Study Using a Clinician-Developed Digital Monitoring System","HANDREHPREDICT","Inclusion Criteria:\n\n* Adults aged 18 years or older\n* Hand or upper extremity pathology requiring rehabilitation, including but not limited to: flexor or extensor tendon injuries, peripheral nerve injuries or compression syndromes (including carpal tunnel syndrome, cubital tunnel syndrome), distal radius fractures, metacarpal or phalangeal fractures, joint injuries and instabilities, arthropathy (osteoarthritis, rheumatoid arthritis), trapeziometacarpal osteoarthritis, trigger finger, Dupuytren's disease, DeQuervain tenosynovitis, lateral epicondylitis and post-surgical upper extremity conditions\n* Under clinical responsibility of the principal investigator at the Faculty of Physical Therapy and Rehabilitation, Hacettepe University\n* Expected to attend minimum 8 rehabilitation sessions\n* Able to provide written informed consent\n\nExclusion Criteria:\n\n* • Active psychiatric illness precluding participation or completion of assessment tools\n\n  * Severe cognitive impairment precluding understanding of patient-reported outcome measures\n  * Literacy difficulties preventing self-completion of questionnaires\n  * Concurrent enrollment in another interventional clinical study\n  * Refusal to provide written informed consent",{"count":79,"type":22},60,"OBSERVATIONAL","This study investigates whether early changes observed during the first weeks of hand and upper extremity rehabilitation can predict patient outcomes months later. In rehabilitation practice, clinicians make numerous decisions each session regarding exercise type, frequency, duration, and treatment approach. Most of these decisions are currently made without systematic longitudinal data. This study addresses three fundamental questions using data collected during routine clinical care: (1) Can the rate of improvement in the first weeks of treatment predict functional status months later, across both session-based and milestone-based time points? (2) Are there meaningfully different recovery profiles among hand rehabilitation patients? (3) Is there measurable variation in clinical decision-making among patients with similar profiles, and does this variation relate to outcomes? A digital patient monitoring platform developed by the principal investigator, a physiotherapist and academic researcher specializing in hand rehabilitation serves as the data collection infrastructure. The platform records standard clinical assessment measures in a structured format and has been in active clinical use at Hacettepe University prior to this study. For research purposes, the system has been expanded to include structured capture of patient-reported outcomes, patient global impression of change, treatment protocol coding, home exercise adherence, and automated calculation of early response metrics.\n\nThis is a 12-month prospective observational cohort study enrolling a minimum of 60 patients. Data are stored securely on the university's institutional network. Patients are anonymized using identification codes. The study is subject to Hacettepe University Ethics Committee approval and participant informed consent. Findings are expected to generate evidence supporting data-driven clinical decision-making in rehabilitation and to provide a feasibility foundation for a larger multi-center study.",[83,84,85,86,87,88,89,90,91,92,93,94,28,95,96,97,98,99,100],"Hand","Hand Therapy","Upper Extremity","Prediction Models","Hand Injuries","Hand Injuries and Disorders","Hand Arthritis","Tendon Injuries","Wrist Fractures","Carpal Tunnel Syndrome (CTS)","Peripheral Nerve Injuries","Upper Extremity Injuries","Finger Injuries","Trigger Finger","Trapeziometacarpal (TMC) Arthrosis","DeQuervain's Tenosynovitis","Cubital Tunnel Syndrome","Postoperative Rehabilitation",[102,103,104,105,106],"digital health monitoring","real-world evidence","clinical decision support","upper extremity rehabilitation","early response prediction","2026-04-03",{"date":109,"type":37},"2026-04-13",{"date":111,"type":22},"2026-06-15",{"date":113,"type":22},"2027-06-01",{"name":115,"class":44},"Hacettepe University",{"id":117,"slug":118,"hasResults":11,"nctId":119,"briefTitle":120,"officialTitle":121,"acronym":4,"eligibilityCriteria":122,"healthyVolunteers":17,"sex":18,"minAge":19,"maxAge":123,"enrollmentInfo":124,"targetDuration":4,"studyType":80,"phases":4,"briefSummary":126,"conditions":127,"keywords":4,"overallStatus":59,"whyStopped":4,"lastUpdateSubmitDate":128,"lastUpdatePostDateStruct":129,"startDateStruct":131,"completionDateStruct":133,"leadSponsor":135,"locationsCount":69},"100591284","hand-held-dynamometer-assessment-e-sports-grip-asymmetry-index-as-a-predictor-of-wrist-pain-100591284","NCT06978426","Hand-Held Dynamometer Assessment: E-Sports Grip-Asymmetry Index as a Predictor of Wrist Pain","Evaluation of Grip Strength Asymmetry Index in Professional E-Sports Athletes as a Predictive Measure for Wrist Pain","Inclusion Criteria:\n\n* Professional e-sports athletes (receiving compensation for gaming activities)\n* Age between 18 and 30 years\n* Gaming for at least 35 hours per week\n* For Pain Group: Reports wrist pain rated ≥3\u002F10 on VAS during gaming activities\n* For No-Pain Group: Reports minimal to no wrist pain (\\\u003C3\u002F10 on VAS) during gaming activities\n\nExclusion Criteria:\n\n* History of neurologic disease\n* History of rheumatic disease\n* Previous wrist surgery\n* Recent wrist trauma (within 3 months)\n* Use of pain medication within 24 hours of assessment\n* Inability to perform grip strength testing","30 Years",{"count":125,"type":22},56,"This cross-sectional study investigates whether a simple Grip-Asymmetry Index (GAI) can predict self-reported wrist pain in professional e-sports athletes. Professional gamers (aged 18-30) who play at least 35 hours per week will be assessed using a Jamar dynamometer to measure maximal grip force in both hands. The study will compare GAI between two groups: those with wrist pain (≥3\u002F10 on Visual Analog Scale during play) and those without pain. A GAI cutoff value for predicting wrist pain risk will be established through ROC analysis, with additional factors such as gaming hours, BMI, and sex incorporated into a multivariable logistic regression model.",[28],"2025-05-10",{"date":130,"type":37},"2025-05-18",{"date":132,"type":22},"2025-06-01",{"date":134,"type":22},"2025-12-01",{"name":136,"class":44},"Ahram Canadian University",{"id":138,"slug":139,"hasResults":11,"nctId":140,"briefTitle":141,"officialTitle":141,"acronym":4,"eligibilityCriteria":142,"healthyVolunteers":11,"sex":143,"minAge":144,"maxAge":145,"enrollmentInfo":146,"targetDuration":4,"studyType":23,"phases":148,"briefSummary":149,"conditions":150,"keywords":152,"overallStatus":59,"whyStopped":4,"lastUpdateSubmitDate":157,"lastUpdatePostDateStruct":158,"startDateStruct":160,"completionDateStruct":162,"leadSponsor":164,"locationsCount":69},"100555249","effects-of-pain-neuroscience-education-and-standard-rehabilitation-regime-in-patients-of-carpal-tunnel-syndrome-100555249","NCT06509633","Effects of Pain Neuroscience Education and Standard Rehabilitation Regime in Patients of Carpal Tunnel Syndrome","Inclusion Criteria:\n\n* age between 20\\_40 years old.\n* Medical diagnosis of moderate to severe CTS.\n* Symptoms of CTS since 1month\n* Unilateral or bilateral symptoms\n* Availability and access to the hospital.\n\nExclusion Criteria:\n\n* Inability to understand instructions, neurological conditions of the central nervous system (e.g. stroke, spinal cord injury)\n* Patients on treatment with alternative therapies\n* Previous participation in a research program\n* Previous surgery on the affected upper limb","FEMALE","20 Years","50 Years",{"count":147,"type":22},30,[25],"The aim of this study is to check the effects of Pain Neuroscience education and standard rehabilitation regime in patients of carpal tunnel syndrome.",[28,151],"Carpal Tunnel Syndrome",[153,154,155,156],"Carpal tunnel syndrome","Compression","Pain neuroscience education","Median nerve","2024-07-18",{"date":159,"type":37},"2024-07-19",{"date":161,"type":37},"2024-02-01",{"date":163,"type":22},"2024-11-10",{"name":165,"class":44},"Riphah International University",{"id":167,"slug":168,"hasResults":11,"nctId":169,"briefTitle":170,"officialTitle":171,"acronym":172,"eligibilityCriteria":173,"healthyVolunteers":11,"sex":18,"minAge":174,"maxAge":175,"enrollmentInfo":176,"targetDuration":178,"studyType":80,"phases":4,"briefSummary":179,"conditions":180,"keywords":4,"overallStatus":59,"whyStopped":4,"lastUpdateSubmitDate":184,"lastUpdatePostDateStruct":185,"startDateStruct":187,"completionDateStruct":189,"leadSponsor":191,"locationsCount":69},"100390951","the-canadian-prospective-pragmatic-perilunate-outcomes-trial-100390951","NCT04370626","The Canadian Prospective Pragmatic Perilunate Outcomes Trial","The Canadian Prospective Pragmatic Perilunate Outcomes Trial (The C3PO Trial)","C3PO","Inclusion Criteria:\n\n* The subject is 14 years of age or older\n* The subject has been clinically diagnosed with a perilunate injury\n* The subject is willing to adhere to the study protocol including required post-operative therapy, all scheduled follow-up visits, evaluations, and questionnaires (if applicable).\n\nExclusion Criteria:\n\nThere will be no limiting exclusion criteria.","14 Years","120 Years",{"count":177,"type":22},450,"10 Years","This is a unique three-fold prospective and retrospective study. With this approach, all previous and current PLIs presented at participating study sites will have the potential to be included in the study. Our goal is to collect all relevant injury and surgical parameters of the Perilunate spectrum. The investigators plan to identify each hospital within Canada that normally treats PLIs and to record injury and demographic information on each PLI that occurs in this country over a two to three-year period. Our protocol includes scheduled two, five, and 10-year follow-up intervals.",[28,181,182,183],"Carpal Bone Fracture","Dislocation of Wrist","Trauma","2022-11-18",{"date":186,"type":37},"2022-11-23",{"date":188,"type":37},"2020-09-01",{"date":190,"type":22},"2026-12-31",{"name":192,"class":44},"University of Calgary"]