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Median Neuropathy clinical trials

View clinical trials related to Median Neuropathy.

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NCT ID: NCT06012630 Completed - Clinical trials for Median Nerve Entrapment

Carpal Tunnel Syndrome Evaluation With Ultrasound in Rheumatoid Arthritis Patients

Start date: January 15, 2023
Phase:
Study type: Observational [Patient Registry]

In rheumatoid arthritis (RA) patients, the diagnosis of Carpal tunnel syndrome (CTS) was made based on clinical findings and physical examinations. Then, the cross-sectional areas of the participants' median nerves from different levels were measured. Meidolateral and anteroposterior diameter were measured at the level of the carpal tunnel inlet. Flattening ratio was calculated. wrist to forearm ratio and wrist to forearm difference were calculated. The obtained data were compared between RA with CTS, RA without CTS and healthy control.

NCT ID: NCT05838807 Completed - Clinical trials for Carpal Tunnel Syndrome

Thermal and Pulsed Ultrasound for Carpal Tunnel Syndrome

Start date: May 28, 2023
Phase: N/A
Study type: Interventional

This study will be a Randomized controlled trial with a sample size of at least 100 individuals with carpal tunnel syndrome. Participants will be randomized to receive either thermal ultrasound, pulsed ultrasound, a combination of both, or a placebo treatment for 10 minutes, three times per week, for 4 weeks. Outcome measures will include pain intensity, functional status, and nerve conduction studies. Outcome measures will be assessed at baseline, 4 weeks, and 8 weeks.

NCT ID: NCT05222126 Completed - Clinical trials for Carpal Tunnel Syndrome

Efficacy of Ultrasound-Guided Hydrodissection in Carpal Tunnel Syndrome

Start date: September 20, 2022
Phase: N/A
Study type: Interventional

The aim of our study is to determine the effectiveness of US-guided hydrodissection of the median nerve in different contents and volumes in patients diagnosed with mild to moderate carpal tunnel syndrome.

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: NCT04324281 Completed - Clinical trials for Cervical Radiculopathy

Myth of Double Crush Syndrome in Median Nerve

cadaveric
Start date: January 5, 2020
Phase:
Study type: Observational

There is relation between the cervical radiculopathy and carpal tunnel syndrome and why the referred pain is fall at carpal tunnel not at elbow.

NCT ID: NCT04218175 Completed - Clinical trials for Median Nerve Disease

Effects of Neuromobilization on Median Nerve Elasticity

Start date: November 10, 2019
Phase: N/A
Study type: Interventional

Purpose: The aim of this study was to investigate the effect of median nerve neuromobilization on median nerve elasticity using shear wave elastography. Methods: The study included 36 healthy volunteers (72 upper extremities) aged 18-30 years. Inclusion criteria; no known systemic neuromuscular and metabolic diseases, no nerve impingement syndrome, and no upper extremity bone-tendon-muscle surgery in the last six months. Sociodemographic data of the participants were recorded. Wrist flexion and extension bilaterally with universal goniometer and finger grip strength bilaterally were measured with pinchmeter. Median Nerve Stress Test was performed. Median nerve elasticity was measured by Shear Wave Ultrasound Elastography. The extremity of the dominant side as a study group and the non-dominant side as a control group were measured bilaterally. Median nerve neuromobilization (stretching (n = 18) and shifting (n = 18)) was applied to the upper extremities of the dominant side. The application was carried out as 3 sets in one session. Evaluations were repeated after application.

NCT ID: NCT02553811 Completed - Clinical trials for Carpal Tunnel Syndrome

Diagnosis of Carpal Tunnel Syndrome: Effectiveness of Diagnostic Tests. Clinical Trial of Accuracy

DCTS
Start date: October 2015
Phase: N/A
Study type: Interventional

There is no golden universal standard for the diagnosis of Carpal Tunnel Syndrome (CTS). In this scenario, for a comparison of the effectiveness of the principal diagnostic tests CTS should determine how they affect the likelihood of disease through a clinical accuracy trial of good methodological quality in order to get answers to what is the best diagnostic strategy in clinical CTS practice. The paresthesia in nerve distribution territory median hands is the most common symptom in patients with CTS. The nuisance caused by paresthesia directly affects the quality of life of patients and impairs daily manual activities and sleep quality. To evaluate the remission of paresthesia is a major clinical criterion for improved STC being an expected relevant outcome for the patient. This study evaluated and compared the diagnostic accuracy of the ultrasonography (US) and electromyography (EMG), considering the postoperative status of remission of paresthesia as the reference standard in the diagnosis of CTS.

NCT ID: NCT01895621 Completed - Clinical trials for Median Neuropathy, Carpal Tunnel

Postoperative Alpha Lipoic Acid in the Carpal Tunnel Syndrome: a Randomized Controlled Trial.

Start date: March 2013
Phase: Phase 4
Study type: Interventional

The postoperative course of the decompression of the median nerve in the carpal tunnel syndrome can sometimes be complicated by pain, paresthesias and other unpleasant symptoms, or may be characterized by a slow recovery of nerve function. Lipoic acid is considered to be a powerful and effective antioxidant with neuroprotective and neurotrophic properties. Dietary supplementation with lipoic acid helps reduce the damage to the nervous structure. Its action as a dietary supplement may positively modulate and accelerate healing after decompression of the median nerve. The aim of the study is to explore any possible effects of this molecule in the postoperative period after decompression of the median nerve at the wrist. Patients will be enrolled with proven carpal tunnel syndrome. By means of randomization, patients will be placed into one of two groups: Group A: surgical decompression of the median nerve followed by alpha lipoic acid, 800 mg daily for 40 days. Group B: surgical decompression of the median nerve followed by treatment with placebo The primary endpoint of the study will be Nerve conduction velocity at 3 months after surgery after 50 days of discontinuing treatment with alpha lipoic acid (TIOBEC) / PLACEBO.

NCT ID: NCT01394822 Completed - Clinical trials for Carpal Tunnel Syndrome

Neuromuscular Ultrasound for Focal Neuropathies

Start date: September 2011
Phase: N/A
Study type: Observational

The purpose of this study is to determine if a new diagnostic technique, called neuromuscular ultrasound, can improve our ability to diagnose focal nerve disease.