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Influence of Pronator Teres Release on Treatment of Median Nerve Compression Neuropathy

The Influence of Pronator Teres Release in the Treatment of Median Nerve Compression Neuropathy: A Randomized Prospective Study

Status
UNKNOWN
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01562860
Enrollment
100
Registered
2012-03-26
Start date
2010-07-31
Completion date
2019-07-31
Last updated
2018-01-25

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Median Nerve Compression

Keywords

median nerve, carpal tunnel syndrome, Pronator Teres Release

Brief 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.

Interventions

PROCEDUREPronator Teres Release

Surgical release of median nerve compression

PROCEDUREdual compression release

Both the carpal tunnel compression and the pronator teres compression will be released on the same day.

PROCEDUREmedian nerve release only

only the carpal tunnel compression is released

Sponsors

Christine M. Kleinert Institute for Hand and Microsurgery
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* 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

Design outcomes

Primary

MeasureTime frameDescription
Symptom severity and functional status score (Brigham and Women's Carpal Tunnel Questionnaire)12 monthsThe 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.

Countries

United States

Contacts

Primary ContactTuna Ozyurekoglu, MD
tozyurekoglu@cmki.org502-561-4263
Backup ContactMillicent L Horn, BS
mhorn@cmki.org502-562-0307

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026