Skip to main content
OpenTrials
Completed

NCT Number: NCT00803257

Effect of Lumbrical Stretching on Carpal Tunnel Syndrome

Symptoms of CTS occur when any condition decreases the size of the carpal canal or increases the volume of the structures within the carpal canal, compressing the median nerve. One cause of the symptoms of CTS is the incursion of the lumbrical muscles of the hand into the carpal canal. Individuals with CTS tend to have tight lumbrical muscles which increase this incursion, thereby increasing CTS symptoms. An intervention designed to reduce the incursion of the lumbrical muscles should have an effect on the symptoms of CTS.

The purpose of this study is to systematically examine the effect of an intensive lumbrical muscle intervention, splinting to prevent lumbrical muscle incursion and lumbrical muscle exercises, on the symptoms of CTS. This project will be a randomized clinical trial to evaluate the effectiveness of a home program targeting the lumbrical muscles. One hundred and twenty subjects will be assigned to one of 4 groups: Group 1 will receive a home program of lumbrical muscle stretches combined with a lumbrical positioning splint; Group 2 will receive a home program of lumbrical muscle stretches combined with a night wrist cock-up splint; Group 3 will receive a home program of general stretches combined with a lumbrical positioning splint; and Group 4 will receive a home program of general stretches combined with a night wrist cock-up splint. After 1 month, 3 months, and 6 months the groups will be compared to determine if there is a significant reduction in symptoms between the groups.

Completed

Looking for future studies?

Notify Me

Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

University of Pittsburgh

Pittsburgh, Pennsylvania, 15260, United States

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • At least 18 yo
  • Clinical symptoms of Carpal tunnel syndrome (CTS)
  • Positive Tinel's, Phalen's, or Durkin's test
  • Absence of thenar atrophy
  • 2 pt discrimination of 5mm or less

Exclusion criteria

  • Persons needing immediate CTS surgery
  • Pregnancy
  • Compressive neuropathy in the ipsilateral arm
  • Diabetes
  • prior CTS release
  • Non-English speaking

Treatment and study plan

Lumbrical splint and Lumbrical exercises

Other

Subjects receive one of four possible interventions - Dose and Frequency are the same for each

Primary outcomes

  1. Carpal Tunnel Syndrome Symptom Severity and Functional Status Scale (CTS-SSFS)

    Time frame: 1 month

Sponsors and collaborators

Lead sponsor

University of Pittsburgh

Other

Collaborators

  • Arthritis Foundation

Registry information

Important dates

Study start
2008
Primary completion
2011
Study completion
2011
First posted
Dec 5, 2008
Registry last updated
Jun 13, 2012

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.