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Cubital Tunnel Syndrome clinical trials

View clinical trials related to Cubital Tunnel Syndrome.

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NCT ID: NCT02566616 Withdrawn - Clinical trials for Cubital Tunnel Syndrome

Electrical Nerve Stimulation of the Ulnar Nerve

ESTIM
Start date: November 2015
Phase: N/A
Study type: Interventional

Cubital tunnel syndrome is caused by compression of the ulnar nerve at the elbow. This leads to symptoms such as chronic hand weakness, numbness and pain. This is usually treated with a surgical procedure where the nerve is decompressed. Research has shown that nerve simulators speed up the recovery of nerves following injury. The purpose of our research is to examine the difference in patient outcomes after the nerve decompression surgery with and without nerve stimulation. Our research questions is: What are the differences in long term functional outcomes of patients that have ulnar nerve decompression surgery with and without nerve stimulation?

NCT ID: NCT02466841 Withdrawn - Clinical trials for Cubital Tunnel Syndrome

Prospective Comparison of Techniques for Cubital Tunnel Release

Start date: August 2015
Phase:
Study type: Observational

Compression of the ulnar nerve at the elbow (cubital tunnel syndrome) is the second most common compressive neuropathy of the upper extremity (carpal tunnel is the most common). Patients who fail conservative treatment (activity modification, splinting, medications) are offered cubital tunnel release. There are multiple techniques to decompress the ulnar nerve at the elbow, but the ideal release has not been determined. These techniques vary from simple decompression of the nerve (in-situ release, endoscopic release), to decompressing the nerve and moving it anteriorly to take tension off the nerve (subcutaneous transposition, sub-fascial transposition, sub muscular transposition), and removing part of the medial epicondyle (medial epicondylectomy). Each procedure has purported benefits and also potential complications. Simple in-situ release has the benefit of shorter operative times and less surgical dissection, however, the nerve may subluxate post-operatively and cause persistent pain. Procedures to move the nerve (subcutaneous transposition, sub-fascial transposition, sub muscular transposition) prevent subluxation and take tension off the nerve, however, they require more dissection, larger incisions, and also partially devascularize the nerve. Medial epicondylectomy prevents subluxation and decompresses the nerve, but some patients may have a prolonged recovery and persistent pain from removing part of the bone. The purpose of this study is to prospective evaluate patients undergoing cubital tunnel release according to the standard practice and preference of their surgeon. The investigators plan to compare the different techniques at standard post-operative intervals.

NCT ID: NCT01893164 Recruiting - Clinical trials for Cubital Tunnel Syndrome

Comparison of Different Surgical Treatments for Different Scales of Cubital Tunnel Syndrome

Start date: July 2013
Phase: N/A
Study type: Interventional

The purpose of this study is to determine which is the best surgery to treat different severity scales of cubital tunnel syndrome.

NCT ID: NCT01781494 Withdrawn - Clinical trials for Cubital Tunnel Syndrome

Immobilization Versus Immediate Motion After Anterior Submuscular Ulnar Nerve Transposition

Start date: January 2014
Phase: N/A
Study type: Interventional

The goal of this study is to test the hypothesis that immediate elbow motion is safe after anterior submuscular ulnar nerve transposition, and will not result in disruption of the repaired flexor pronator origin, under which the nerve is placed. The advantages of immediate elbow motion after submuscular ulnar nerve transposition for performing activities of daily living and self-care are evident, however theoretical advantages include early "gliding" of the transposed ulnar nerve with a lower risk of nerve adhesions and subsequent traction neuritis, as well as improved blood flow and quicker, more complete, recovery of nerve function. A group of 44 consecutive patients that are determined to be candidates for anterior submuscular ulnar nerve transposition based on history, positive findings on physical examination, and confirmatory electrodiagnostic testing will be prospectively randomized to either immediate motion or long arm cast immobilization after surgery. All patients will be counseled about the two postoperative treatment options (immobilization followed by protected range of motion versus immediate range of motion), risks involved with each treatment protocol, postoperative follow-up and need for radiographs. If they choose not to participate, they will be treated by the same postoperative protocol currently used by the principal investigator: arm sling at rest for six weeks with intermittent active assisted range of motion exercises.

NCT ID: NCT01693094 Suspended - Clinical trials for Carpal Tunnel Syndrome

A Randomized Trial Measuring the Effect of Decision Aids on Patients' Satisfaction, Conflict of Decision-making and Clinical Outcome

Start date: June 10, 2014
Phase: N/A
Study type: Interventional

The investigators plan a prospective randomized controlled study that compares the treatment decisions made by patients who receive decision aids, as compared to patients treated with usual care and the American Society for Surgery of the Hand brochures. The investigators expect to enroll 126 patients.

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.

NCT ID: NCT01109901 Completed - Clinical trials for Cubital Tunnel Syndrome

Comparison of Effect of Anterior Subcutaneous and Submuscular Transposition on Cubital Tunnel Syndrome

Start date: October 2008
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine which surgical method is better for cubital tunnel syndrome in outcomes.

NCT ID: NCT00184158 Completed - Clinical trials for Cubital Tunnel Syndrome

Treatment for Cubital Tunnel Syndrome

Start date: January 2005
Phase: N/A
Study type: Interventional

The researchers want to find out the best treatment for cubital tunnel. The researchers establish the degree of nerve compression and then the patients are randomised to different treatment alternatives, ranging from conservative to operative treatments. The study is performed at 5 different hospitals in Norway.