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Cubital Tunnel Syndrome clinical trials

View clinical trials related to Cubital Tunnel Syndrome.

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NCT ID: NCT04658511 Not yet recruiting - Clinical trials for Cubital Tunnel Syndrome

Presence of the Arcade of Struthers on Preoperative Ultrasound

Start date: March 31, 2021
Phase: N/A
Study type: Interventional

To determine the correlation between the presence of the arcade of Struthers on preoperative ultrasound and during endoscopic surgery for cubital tunnel syndrome, and to determine the reliability of a portable ultrasound probe to detect the arcade of Struthers in the arm.

NCT ID: NCT04647058 Withdrawn - Clinical trials for Cubital Tunnel Syndrome

Randomized Trial of Supercharged End-to-Side Anterior Interosseous Nerve Transfer for Severe Cubital Tunnel Syndrome

Start date: April 5, 2021
Phase: N/A
Study type: Interventional

Functional motor recovery distal to a peripheral nerve lesion is predicated upon time to reinnervation of the motor end plate and the number of regenerate axons that reach the target. Supercharged end-to-side (SETS) transfer of the anterior interosseous nerve to the motor fascicle of the ulnar nerve at the level of the distal forearm has been proposed as an adjunct procedure in severe cubital tunnel syndrome to augment motor recovery of the ulnar-innervated intrinsic muscles. Multiple Level IV Therapeutic studies and a systematic review of Level IV Therapeutic studies have reported favorable clinical and electrodiagnostic outcomes following SETS for cubital tunnel syndrome, with low rates of complications. However, in the absence of controls, it remains unclear what proportion of the observed intrinsic motor recovery is attributable to the SETS procedure. The objective of this randomized trial is to compare the results of ulnar nerve decompression with or without SETS for severe cubital tunnel syndrome.

NCT ID: NCT04470245 Recruiting - Clinical trials for Cubital Tunnel Syndrome

Cubital Tunnel Syndrome and Diffusion MRI: A Proof of Concept Study

Start date: July 8, 2019
Phase: N/A
Study type: Interventional

Cubital Tunnel Syndrome (CTS) results from compression of the ulnar nerve at the elbow (colloquially termed the "funny bone"). CTS affects up to 6% of the population and 6000 patients undergo surgery annually in the UK. Surgery is the only proven treatment for CTS, although up to 30% of patients do not improve. Therefore, there is a pressing need to develop a reliable test to diagnose CTS to improve the selection of patients for surgery. New techniques in the field of magnetic resonance imaging (MRI) allow the visualisation of nerve structure and function. Diffusion tensor MRI, also known as diffusion tensor imaging (DTI), can diagnose CTS with superior diagnostic accuracy and could enable the reliable diagnostic of CTS, improving the selection of patients for surgery. The study will include healthy volunteers (to refine the scanning sequence) and patients undergoing surgery for CTS. Patients will be scanned preoperatively and postoperatively using cutting-edge diffusion MRI techniques. The primary outcome will be change in the MRI-derived diffusion metrics following surgery. Secondary outcomes will consider how MRI relates to patient-reported outcomes and conventional clinical tests (ultrasound and nerve conduction studies). Leeds is the ideal location for this research because a) Leeds institutions are the most highly cited organisations in musculoskeletal research, b) Leeds houses the National Centre for Hyperpolarized MRI and a state-of-the-art MRI scanner, and c) Leeds is an internationally recognised centre of excellence for complex upper limb surgery.

NCT ID: NCT04322448 Completed - Clinical trials for Cubital Tunnel Syndrome

Mechanomyography for Predictor of Prognosis in CuTS and PND Patients

Start date: August 3, 2020
Phase:
Study type: Observational

The study will be a non-blinded two cohort design consisting only of symptomatic patients with CuTS or compressive peroneal neuropathy or in need of peroneal nerve decompression. The first cohort will be - patients with CuTS. Evaluation of each CuTS patient will include assessment by the treating surgeon and a certified hand therapist. Patients who have clinical examination and history consistent with a diagnosis of CuTS based on subjective and functional assessment outlined below will be consented to this study. The second cohort will be patients in need PND for compressive neuropathy of peroneal nerve. PND patients will be evaluated by clinical exam and have imaging with high resolution ultrasound or MRI negative for mass lesion.

NCT ID: NCT03651609 Recruiting - Clinical trials for Peripheral Nervous System Diseases

Treatment for Ulnar Neuropathy at the Elbow

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

The purpose of the study is to investigate utility and appropriateness of treatment interventions taking into account the presumed mechanisms of two main varieties of ulnar neuropathy at the elbow (UNE). The investigators hypothesize that in patients with UNE under the humeroulnar aponeurosis (HUA) surgical HUA release (simple decompression) is superior to conservative treatment. By contrast, in patients with UNE at the retroepicondylar (RTC) groove surgical HUA release (simple decompression) should not be superior to conservative treatment.

NCT ID: NCT03629470 Completed - Clinical trials for Cubital Tunnel Syndrome

Effectiveness of Nerve Glide Exercises on Cubital Tunnel Syndrome

Start date: November 9, 2020
Phase: N/A
Study type: Interventional

The objective of this study is to determine if nerve glide exercises in patients with cubital tunnel syndrome can improve pain, paraesthesias and reduce the need for future surgery. Cubital tunnel syndrome is a common form of peripheral neuropathy caused by compression of the ulnar nerve at the elbow. Surgical intervention is typically reserved for those with severe symptoms, but many cases can be treated with non-operative measures. This study will look at the efficacy of nerve glide exercises in the management of cubital tunnel syndrome. 70 subjects with cubital tunnel syndrome will be enrolled and randomized into groups receiving either standard conservative measures or standard measures in addition to nerve glide exercises. Outcomes will be measured 6 months after initiation of treatment with questionnaires on clinical symptoms and function to see if there is a difference between the two groups.

NCT ID: NCT02995382 Withdrawn - Clinical trials for Cubital Tunnel Syndrome

Health-Related Quality of Life in Cases of Cubital Tunnel Syndrome

Start date: April 2023
Phase: N/A
Study type: Interventional

This study aims to determine the Health Related Quality of life (HRQOL) (the physical, mental, emotional and social functioning) of patients with cubital tunnel syndrome following anterior intramuscular transposition, after one year.

NCT ID: NCT02801461 Completed - Clinical trials for Cubital Tunnel Syndrome

The Effect of ESWT for Cubital Tunnel Syndrome

Start date: October 2016
Phase: N/A
Study type: Interventional

The shock wave is a new and potential intervention for the reinnervation of peripheral nerve. The purpose of this study was to assess the effect of extracorporeal shock wave therapy on cubital tunnel syndrome.

NCT ID: NCT02739945 Completed - Clinical trials for Ulnar Nerve Compression, Cubital Tunnel

Sonographic Examination Cubital Tunnel Release

SPECTRE
Start date: May 2011
Phase: Phase 3
Study type: Interventional

The investigators want to compare changes in cross-sectional area (CSA) of the ulnar nerve at the elbow after open release or endoscopic release.

NCT ID: NCT02677506 Completed - Clinical trials for Cubital Tunnel Syndrome

Infraclavicular or Supraclavicular Brachial Plexus Blocks for Elbow Surgery

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

This study compares the infraclavicular approach to supraclavicular approach of brachial plexus block for elbow surgery.