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Carpal Tunnel Syndrome clinical trials

View clinical trials related to Carpal Tunnel Syndrome.

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NCT ID: NCT04993703 Completed - Clinical trials for Carpal Tunnel Syndrome

Effect of Kinesiotaping and Night Splinting in Patients With Carpal Tunnel Syndome

Start date: August 10, 2021
Phase: N/A
Study type: Interventional

Carpal tunnel syndrome (CTS) which is defined as a symptomatic compression neuropathy of the median nerve at the level of the wrist. Different types of splints are used for improving the function and decreasing the pain intensity and symptoms in the rehabilitation of patients with CTS. However effectiveness of treatment by taping has never been investigated in physiotherapy and rehabilitation. The aim of this study was to compare the short-term effect of conventional physiotherapy only, and also kinesio taping and night splinting in patients with CTS.

NCT ID: NCT04976998 Recruiting - Clinical trials for Carpal Tunnel Syndrome

Role of Ultrasonography in the Diagnosis of Carpal Tunnel Syndrome

Start date: August 29, 2021
Phase:
Study type: Observational

This prospective study aims to evaluate the median nerve in Carpal Tunnel Syndrome by high-frequency ultrasound and color Doppler in comparison with clinical and Nerve conduction studies.

NCT ID: NCT04969393 Completed - Pregnancy Related Clinical Trials

Effects of High Intensity Laser on Mechanical and Physiological Findings in Pregnant Women With Carpal Tunnel Syndrome

Start date: April 30, 2021
Phase: N/A
Study type: Interventional

This study will propose a novel approach to treat pregnant women with mild to moderate carpal tunnel syndrome (CTS) using the recently introduced High intensity laser therapy with its deep penetration and high-power characteristics. It's hopeful that the results of this study can fill the gap of knowledge surrounding the conservative treatment options for CTS in order to help patients restore their nerve function properly and promote new ways of addressing CTS.

NCT ID: NCT04967144 Completed - Clinical trials for Carpal Tunnel Syndrome

Carpal Tunnel Syndrome, Right/Left Judgement

Start date: July 19, 2021
Phase:
Study type: Observational

The discrimination of the right/left side of the body is related to the integrity of the motor and somatosensory areas at the cortical and subcortical levels. Although some studies have shown that there may be an effect on the right/left representation at the cortical and subcortical levels in cases that cause severe neuropathy and neuropathic pain, this effect has not been proven in milder neuropathies. In this study, the effect on right/left side discrimination will be investigated even in cases with carpal tunnel syndrome. Additionally, the investigators aimed to assess the relationship between right/left discrimination and symptom severity.

NCT ID: NCT04961281 Completed - Chronic Pain Clinical Trials

Dexmedetomidine Versus Triamcinolone Treatment of Carpal Tunnel Syndrome

Start date: July 22, 2021
Phase: N/A
Study type: Interventional

Carpal tunnel syndrome (CTS) is a common mononeuropathy due to entrapment of the median nerve in the carpal tunnel. a lot of modaleties are available for treatment of mild to moderate CTS.

NCT ID: NCT04949373 Completed - Clinical trials for Carpal Tunnel Syndrome

High Intensity Laser Therapy in Carpal Tunnel Syndrome

Start date: June 1, 2021
Phase: N/A
Study type: Interventional

This research aims to investigate the effect of high-intensity laser therapy on pain, function, nerve conduction studies and grip strength in patients with idiopathic carpal tunnel syndrome.

NCT ID: NCT04924348 Completed - Anesthesia, Local Clinical Trials

WALANT Procedure in Carpal Tunnel Release

Start date: December 2, 2020
Phase: N/A
Study type: Interventional

The possible benefits expected from the use of the WALANT procedure are a decrease in intraoperative pain at the surgical site, a decrease in hospitalization time, and a decrease in the time required to lift the anesthesia postoperatively. The risks identified are those inherent to each type of anesthesia (WALANT or traditional ALR), as encountered in current practice, and are therefore not specific to the study: risks related to the local anesthetic agent or risks related to the puncture procedure. The main objective is to determine whether the patient's intraoperative pain at the surgical site is less after a WALANT procedure compared to a traditional ALR procedure (axillary or trunk).

NCT ID: NCT04921891 Completed - Clinical trials for Carpal Tunnel Syndrome

Is Perfusion Index an Indicator of Block Success in Ultrasound-guided Infraclavicular Brachial Plexus Block

Start date: April 15, 2014
Phase: N/A
Study type: Interventional

The infraclavicular nerve block, which is frequently preferred in upper extremity surgeries, provides additional advantages such as reduction in opioid consumption by providing analgesic effect in the postoperative period as welll. The success of peripheral nerve blocks is usually assessed by subjective feedback from the patient, and patient cooperation is needed. The aim of this study is to assess whether the perfusion index level, which can be measured noninvasively, can be a predictor of the infraclavicular block success.

NCT ID: NCT04896398 Completed - Clinical trials for Carpal Tunnel Syndrome

The Effect of ESWT in Carpal Tunnel Syndrome

ESWT
Start date: June 1, 2021
Phase: N/A
Study type: Interventional

50 patients who meet the inclusion criteria will be included in this prospective, randomized and controlled study. Demographic information of the patients will be taken and recorded. After the patients are numbered according to the order of application, they will be divided into 2 groups as study and control groups according to randomization with the computer program. A total of 5 sessions of ESWT (1000 shock, 1.6 bar, 5 Hz) will be applied to the study group (1st group) for 2 weeks. Patients will be taught median nerve and tendon shifting exercises and will be asked to do it regularly. Patients in the control group (Group 2) will be asked to perform median nerve and tendon shifting exercises only for the wrist. Patients will be evaluated before treatment, at 4 and 12 weeks after treatment. In the evaluation, Boston Carpal Tunnel Inquiry Form, pain severity assessment with VAS (visual analog scale), neuropathic pain intensity with LANSS scale and median nerve conduction velocity with EMG will be evaluated.

NCT ID: NCT04890119 Recruiting - Clinical trials for Carpal Tunnel Syndrome Bilateral

Prevalence Study of Amyloidosis in Patients With Surgery of Suspect Bilateral Carpal Tunnel (AMYLYONCARP)

AMYLYONCARP
Start date: May 17, 2021
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate the prevalence of amyloidosis in population of patient affected by suspect bilateral carpal tunnel with indication of surgery