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Clinical Validation of a Decompression Prototype Splint for Patients With Carpal Tunel Syndrome

NCT04043780 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 60

Last updated 2020-11-04

No results posted yet for this study

Summary

A multicentric randomized controlled trial has been designed to study the effects of a decompression prototype splint on symptoms, functional capacity and nerve conduction studies in patients with carpal tunnel syndrome.

Conditions

  • Carpal Tunnel Syndrome

Interventions

DEVICE

Decompression prototype splint for carpal tunnel syndrome

This group will wear during 6 weeks a decompression prototype splint. They we be informed to wear it as long as possible during the 6 weeks.

DEVICE

Standard splint for carpal tunnel syndrome

This group will wear during 6 weeks a standard splint. They we be informed to wear it as long as possible during the 6 weeks.

Sponsors & Collaborators

  • Salud Aragon

    collaborator UNKNOWN

  • Universitat de Catalunya

    collaborator UNKNOWN

  • Institut Català de la Salut

    collaborator OTHER

  • Universidad de Zaragoza

    lead OTHER

Principal Investigators

  • Elena Estébanez-de-Miguel, PhD · Universidad de Zaragoza

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
TRIPLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2019-09-24
Primary Completion
2020-03-01
Completion
2020-09-01

Countries

  • Spain

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 NCT04043780 on ClinicalTrials.gov