CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 333 enrolled
Drug / intervention
Web-based surveyother
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT02788734
NCT02788734N/ACompleted

Patient Reported Outcomes Measures (PROM) in Carpal Tunnel Therapies in Patients With Inherited Neuropathies

University of South Florida·observational·Posted Jun 2, 2016·Updated Mar 15, 2018

In Brief

An observational study evaluating Web-based survey for Carpal Tunnel Syndrome and 2 related conditions. Completed, enrolled 333 participants across 1 site.

Detailed Summary

The purpose of this study is to learn about focal compressive median neuropathy at the wrist (Carpal Tunnel Syndrome) and outcomes of therapies (e.g. conservative and surgery) in the upper extremities of patients diagnosed with an inherited neuropathy. All patients enrolled in the Rare Diseases Clinical Research Network (RDCRN) Inherited Neuropathies Consortium (INC) Contact Registry who have marked one of the following disorders: CMT1A, CMT1B, CMT2A, CMT4, CMTX, other known CMT peripheral neuropathy, other unknown CMT peripheral neuropathy, or Hereditary Neuropathy with liability to Pressure Palsies (HNPP), will be invited via email to participate in this online study.

Study Details

Timeline

N/ACompletedFinished
2017201820192020202120222023202420252026
First PostedJun 2, 2016
Enrollment StartJun 1, 2016
Primary CompletionNov 19, 2016
TodayJul 2, 2026
Enrollment to primary: 6 monthsPosted 10.1 years ago

Interventions

Web-based surveyother

This study protocol consists of one anonymous survey. Each participant can complete only one survey. The survey will take approximately 25 minutes to complete. The survey is designed to identify items that best reflect the symptom severity and functional status in patients with CTS and CMT. A unique link to the survey will be included in an email invitation distributed to all adult CMT or HNPP patients self-registered in the RDCRN INC Contact Registry. Upon clicking the link, the participant will be directed to the IRB-approved online consent form. Upon providing consent, the participant will be directed to the online survey.