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Carpal Tunnel Syndrome clinical trials

View clinical trials related to Carpal Tunnel Syndrome.

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NCT ID: NCT03792945 Completed - Clinical trials for Carpal Tunnel Syndrome

Comparison of the Efficacy of Corticosteroid Injection and ESWT in Patients With CTS

Start date: January 20, 2019
Phase: Phase 4
Study type: Interventional

In this study, the investigators aimed to demonstrate the efficacy of ESWT (extracorporeal shock wave therapy) and local corticosteroid injection in patients with carpal tunnel syndrome(CTS) compared to participants receiving only splint and exercise therapy. And the investigators wanted to show that ESWT, a noninvasive treatment modality, is as effective and reliable as local corticosteroid injection, which is the least invasive treatment. Mild and moderate CTS patients will be determined according to American Association of Electrodiagnostic Medicine (AAEM) criteria. 90 idiopathic moderate and mild CTS patients will be included in the study. The participants will be informed about their participation in a study and written informed consent will be obtained.The demographic characteristics and disease duration of the participants will be recorded.The participants will be randomly divided into 3 groups.40 mg of local methylprednisolone (depomedrol) injection will be applied to Group 1 once. And group 1 will also be given a hand wrist rest splint to use for 3 months, especially at night, when not using the hand. ESWT will be applied to Group 2 once a week for a total of 3 weeks and hand wrist rest splints will be given for 3 months especially at night when it is not in use. Group 3 (control group) will be given a hand wrist rest splint to use for 3 months, especially at night, when not using the hand. The evaluations will be repeated before treatment, after the first week after treatment (first ESWT application) and at the 3rd month. Hand grip strength measurement will be performed using Boston carpal tunnel syndrome questionnaire, visual analog scale and dynamometer. Electromyogram (EMG) data will be recorded before and 3 months after treatment. During the trial, the routine will not be excluded.

NCT ID: NCT03782558 Completed - Clinical trials for Carpal Tunnel Syndrome

Validation of the Polish Version of the Boston Carpal Tunnel Syndrome Questionnaire

Start date: January 22, 2019
Phase:
Study type: Observational

Carpal tunnel syndrome is the most common compression neuropathy. The compression of the median nerve occurs in the carpal tunnel and results in pain and other unpleasant sensations in hand and wrist. In more advanced stage, weakness and wasting of the thenar and other muscles innervated by median nerve occurs, which may lead to permanent impairment of manual performance. The Boston carpal tunnel questionnaire (BCTQ) is one of the most commonly used tools for monitoring of the disease progression and of the effect of therapy. Originally created in English, it has been translated into many languages and subsequently validated. Recently the Polish version has been created and the purpose of this study is to validate it.

NCT ID: NCT03781141 Recruiting - Clinical trials for Carpal Tunnel Syndrome

Wound Closure Study in Carpal Tunnel and Trigger Finger Surgery

Start date: December 1, 2019
Phase: N/A
Study type: Interventional

Does a difference in patient satisfaction and cosmetic outcome exist between wound closure with absorbable or non-absorbable sutures.

NCT ID: NCT03779958 Withdrawn - Clinical trials for Carpal Tunnel Syndrome

Alternatives to Hand Therapy for Hand Surgery Patients

Start date: January 12, 2019
Phase:
Study type: Observational

Patients will be asked to use a mobile phone app to conduct their hand therapy after having hand surgery.

NCT ID: NCT03757416 Terminated - Clinical trials for Carpal Tunnel Syndrome

Flexor Tenosynovectomy to Treat Recurrent Carpal Tunnel Syndrome

Start date: February 2016
Phase:
Study type: Observational

The purpose of this study is to collect data on the clinical and functional outcomes of surgical management for recurrent carpal tunnel syndrome (CTS) using flexor tenosynovectomy. It is hypothesized that the outcomes of patients undergoing flexor tenosynovectomy for recurrent CTS will compare favorably to published data regarding alternative types of surgeries for the same condition.

NCT ID: NCT03747510 Completed - Clinical trials for Carpal Tunnel Syndrome

PAVmed CarpX Device Clinical Study

Start date: January 5, 2019
Phase: N/A
Study type: Interventional

To study the safety and feasibility of the CarpX device to divide and release the transverse carpal ligament in order to provide relief for Carpal Tunnel Syndrome (CTS).

NCT ID: NCT03742466 Completed - Chronic Pain Clinical Trials

Local Injection of Ozone Versus Methylprednisolone Acetate in Carpal Tunnel Syndrome of Scleroderma Patients

Start date: November 10, 2018
Phase: N/A
Study type: Interventional

Carpal tunnel syndrome is a common peripheral entrapment neuropathy, this study aims to investigate if, and to what extent local ozone therapy could offer symptom improvement in scleroderma patients with Carpal tunnel syndrome

NCT ID: NCT03730376 Completed - Clinical trials for Carpal Tunnel Syndrome

Decision Making in Hypothetical Carpal Tunnel Syndrome

Start date: October 1, 2018
Phase: N/A
Study type: Interventional

Participants will be presented with a hypothetical scenario of carpal tunnel and asked to make a decision for that case.

NCT ID: NCT03729375 Completed - Pain, Postoperative Clinical Trials

The Effect Of An Anesthetic Procedure On Post Operative Pain Management In Carpal Tunnel Release

CTR
Start date: October 4, 2018
Phase: Phase 1
Study type: Interventional

Carpal Tunnel Syndrome patients undergoing carpal tunnel release surgery performed by the PI will receive intra-operative injections of bupivacaine (Marcaine). Two groups of patients will be randomly selected and will receive either 10cc or 20cc of injection. Their post-operative pain scores and usage of post-operative pain medication will be recorded and analyzed.

NCT ID: NCT03722303 Recruiting - Clinical trials for Carpal Tunnel Syndrome

Lipografting Versus Steroid Injections for Treatment of Carpal Tunnel Syndrome

Start date: December 19, 2016
Phase: Early Phase 1
Study type: Interventional

This study applies the regenerative properties of autologous fat transfer to treat mild to moderate carpal tunnel syndrome in comparison to the current standard of care, corticosteroid treatment. The investigators hypothesize the fat transfer would prevent scar formation and aid in nerve excursion along the canal (while the neoangiogenic and regenerative growth factors could stimulate nerve regeneration) better than the standard of care treatment.