Osteopathic manipulation versus wrist immobilization for carpal tunnel syndrome
Official title: Comparing Efficacy of Osteopathic Manipulation vs. Wrist Immobilization for Carpal Tunnel Syndrome Using Magnetic Resonance Imaging and Patient Perception
Run by New York Institute of Technology · NCT07432750 · Data updated 2026-11-12
This test will see if hands-on osteopathic manipulation or wearing a wrist brace works better to reduce pain, numbness, and loss of function in adults with mild to moderate carpal tunnel syndrome.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 18 Years and up |
| Sex | All |
| Enrollment | 10 (estimated) |
| Sponsor | New York Institute of Technology Academic / other |
| Locations | 1 site (Old Westbury, New York) |
| Status | Recruiting |
| Started | March 2026 |
| Main results expected | August 30, 2026 |
| Study ends | February 28, 2027 |
| Registry record updated | February 25, 2026 |
| Trial ID | NCT07432750 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Adults (18+) with physician-diagnosed mild to moderate carpal tunnel syndrome who meet the Boston Carpal Tunnel Questionnaire score criteria and have not had prior carpal tunnel release are ideal candidates.
✕Probably not a fit
People with severe carpal tunnel syndrome, prior carpal tunnel release, those who found no benefit from bracing, pregnant patients, or those with MRI contraindications are unlikely to benefit or be eligible.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This randomized, single-site study at the New York Institute of Technology compares osteopathic manipulative treatment (OMT) to standard wrist immobilization in adults with mild to moderate carpal tunnel syndrome. Eligible participants must meet symptom thresholds on the Boston Carpal Tunnel Questionnaire and will be randomly assigned to OMT or a wrist brace by drawing a number from a bag. A baseline MRI of the affected wrist will be obtained and volumetric and structural measures of the carpal tunnel and median nerve will be analyzed. Symptom scores and imaging changes will be tracked over the follow-up period to compare outcomes between groups.
Why it matters
Potential benefit: If successful, this could offer a non-surgical option that reduces symptoms and improves hand function for people with mild to moderate carpal tunnel syndrome.
How similar studies have gone: Previous small trials and case series have suggested benefit from manual therapies including osteopathic manipulation for CTS, but large randomized comparisons with bracing and correlated imaging remain limited.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Patients who have been diagnosed with mild/moderate carpal tunnel syndrome * Patients who are over the age of 18 and patients who score at least a 3 in at least one category in both subsections of the Boston Carpal Tunnel Questionnaire. * Exclusion criteria: * Patients who are under the age of 18 * Patients who are pregnant * Patients who have found no benefit to their Carpal Tunnel Syndrome Symptoms with bracing * Patients who have previously undergone Carpal Tunnel Release * Patients who have been diagnosed with osteoporosis, osteomyelitis, underlying bone diseases, severe rheumatoid arthritis or other inflammatory arthritis. * Patients with magnetic resonance imaging specific contraindications include patients with metallic implanted devices or retained metallic foreign bodies, patients with severe and uncontrolled claustrophobia and patients who are pregnant
Where it's running
-
New York Institute of Technology
Old Westbury, New York, United States Recruiting
Study contacts
- Study coordinator: Jordan Keys, DO
- Email: jordan.keys@nyit.edu
- Phone: 1 (805)895-3022
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.