Clinical Trials Directory

Trials / Terminated

TerminatedNCT03757416

Flexor Tenosynovectomy to Treat Recurrent Carpal Tunnel Syndrome

Outcomes After Flexor Tenosynovectomy to Treat Recurrent Carpal Tunnel Syndrome: A Prospective Study

Status
Terminated
Phase
Study type
Observational
Enrollment
2 (actual)
Sponsor
University of Tennessee · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

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.

Detailed description

Primary carpal tunnel release (CTR) is the most common surgical procedure of the hand, but reported rates of symptom recurrence are not uncommon. Many surgical techniques have been proposed and reported for management of carpal tunnel syndrome (CTS) symptom recurrence, however there is a paucity of data on flexor tenosynovectomy for management of recurrent CTS. This study will evaluate clinical and functional outcomes using information from pre- and post-operative physical exams, surgery data, patient-reported satisfaction and symptoms, and scores on functional measures, such as the Disabilities of the Arm, Shoulder, and Hand (DASH) questionnaire.

Conditions

Interventions

TypeNameDescription
OTHERData collectionIf it has been determined that the patient will be undergoing flexor tenosynovectomy for the treatment of recurrent carpal tunnel syndrome, the patient will be asked to participate in this data collection study.

Timeline

Start date
2016-02-01
Primary completion
2018-11-01
Completion
2018-11-01
First posted
2018-11-28
Last updated
2018-11-28

Source: ClinicalTrials.gov record NCT03757416. Inclusion in this directory is not an endorsement.