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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT01562860
Other study ID # 10.0039
Secondary ID
Status Recruiting
Phase Phase 2
First received August 8, 2011
Last updated January 23, 2018
Start date July 2010
Est. completion date July 2019

Study information

Verified date January 2018
Source Christine M. Kleinert Institute for Hand and Microsurgery
Contact Tuna Ozyurekoglu, MD
Phone 502-561-4263
Email tozyurekoglu@cmki.org
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The investigators are comparing two standard of care procedures which can be performed at the same time, or sequentially. The hypothesis being tested is whether simultaneous release of both the carpal Tunnel and the Pronator Teres results in a better outcome in terms of symptom relief and recurrence than Carpal Tunnel Release alone when signs and symptoms of both carpal tunnel and pronator Teres syndromes are present.


Recruitment information / eligibility

Status Recruiting
Enrollment 100
Est. completion date July 2019
Est. primary completion date July 2019
Accepts healthy volunteers No
Gender All
Age group 18 Years to 65 Years
Eligibility - Inclusion Criteria: Positive Tinnels signs over the median nerve at the Carpal Tunnel and Pronator Teres

- Normal two point discrimination

- Over the age of 18 and under the age of 65

Exclusion Criteria:

- Peripheral neuropathy of the median nerve secondary to trauma

- Presence of thoracic outlet syndrome

- Presence of cervical disk disease

- Under the age of 18 and over the age of 65

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Pronator Teres Release
Surgical release of median nerve compression
dual compression release
Both the carpal tunnel compression and the pronator teres compression will be released on the same day.
dual compression release
both procedures will be done on the same day
median nerve release only
only the carpal tunnel compression is released

Locations

Country Name City State
United States Christine M. Kleinert Institute for Hand and Microsurgery Louisville Kentucky

Sponsors (1)

Lead Sponsor Collaborator
Christine M. Kleinert Institute for Hand and Microsurgery

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Symptom severity and functional status score (Brigham and Women's Carpal Tunnel Questionnaire) The primary outcome measure will be the difference between the pre and post operative assessments of the questionnaire, which will represent the degree of improvement as result of the surgical intervention. 12 months