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Safety and Efficacy of a Device for the Relief of Pain Due to Carpal Tunnel Syndrome

NCT03810326 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 40

Last updated 2019-01-18

No results posted yet for this study

Summary

Interventional study to evaluate efficacy and safety of an active splint.

Conditions

  • Carpal Tunnel Syndrome

Interventions

DEVICE

CTR device (tradename named Xtend)

Non invasive active splint

Sponsors & Collaborators

  • Yuinvent Innovations Ltd.

    lead INDUSTRY

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
40 Years
Max Age
80 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2019-01-12
Primary Completion
2020-01-01
Completion
2020-01-01

Countries

  • Israel

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03810326 on ClinicalTrials.gov