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NCT07432750 · ClinicalTrials.gov registry record · NA
Comparing Efficacy of Osteopathic Manipulation vs. Wrist Immobilization for Carpal Tunnel Syndrome
A NA study of Carpal Tunnel Syndrome (CTS), sponsored by New York Institute of Technology.
- Recruiting
- Registry status
- NA
- Development phase
- 10
- Enrollment target
- 1
- Study location
NCT07432750: Recruiting NA study of Carpal Tunnel Syndrome (CTS), sponsored by New York Institute of Technology.
NCT07432750 is a NA study of Carpal Tunnel Syndrome (CTS) that is actively recruiting participants, run by New York Institute of Technology. The registered enrollment target is 10 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (99% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT07432750, a NA study of Carpal Tunnel Syndrome (CTS), is actively recruiting participants, sponsored by New York Institute of Technology.
- RECRUITING
- Registry status
- NA
- Development phase
- 10 participants
- Enrollment target
- 1
- Study location
Study Summary
Carpal Tunnel Syndrome (CTS) can be defined as disruption of the median nerve and is characterized by pain, numbness and tingling of the lateral 3.5 digits of the hand. In severe cases, motor function can also be disrupted. There are many factors that can contribute to the development of CTS: inflammation, compression, bony abnormality, mechanical injury, or certain lifestyle choices. Abnormalities have been proven to be tangibly visible with ultrasound in prior research projects in the form of decreased cross sectional area of the carpal tunnel, flattening of the median nerve, retinacular bowing and increased median nerve intensity. Although CTS has proven to be multifactorial, the standard of care for patients with CTS has historically been wrist immobilization and/or surgical release by endoscopic or open approach. This is despite evidence that osteopathic manipulation techniques have been effective in improving quality of life for patients with CTS. Patients will not be harmed if they are not bracing, as standard of care may include multiple things: bracings vs. OMM vs. surgical release. Our study will take place over the course of 10 weeks. Patients who have been previously diagnosed with mild or moderate carpal tunnel syndrome by a physician previously will be randomly placed into one of two groups: osteopathic manipulative medicine or bracing. If placed in the bracing category, patients will be given a brace and asked to wear it nightly. If placed in the osteopathic manipulative medicine category, patients will be asked to present to the clinic one time a week for 6 weeks. Each time the patient presents to clinic, they will be treated for 30 minutes. for 30 minutes of osteopathic manipulative medicine for 6 consecutive weeks. At the first presentation, patients will obtain a magnetic resonance image of the affected wrist, from which a cross sectional area will be determined. Repeat magnetic resonance image will be obtained at the conclusion of treatment.
Primary Outcome
Objective measures will be in the form of the cross sectional area of the patient's affected carpal tunnel obtained through magnetic resonance imaging. Measurement of the carpal tunnel, obtained by measuring the distance between the transverse carpal ligament and the floor of the tunnel will be obtained. Transverse measurements of the carpal tunnel will be obtained as well. From these measurements, the volume of the carpal tunnel will be determined. Increased carpal tunnel cross sectional area
Conditions Studied
Interventions
- PROCEDURE Osteopathic Manipulative Treatment
- DEVICE Wrist Immobilizer
Study Locations (1)
New York
- New York Institute of Technology - Old Westbury
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 10 participants |
| Start Date | 2026-03 |
| Est. Completion | 2027-02-28 |
| Phase | NA |
What NCT07432750 shows while recruiting
NCT07432750 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 10 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (99% lower).
The record links to 1 condition, with Carpal Tunnel Syndrome (CTS) appearing as the primary indexed condition, and to 2 interventions - of which Osteopathic Manipulative Treatment is the first listed.
NCT07432750 reports a single indexed study location in New York.
Frequently Asked Questions
What is clinical trial NCT07432750 about?
NCT07432750 is a clinical study titled "Comparing Efficacy of Osteopathic Manipulation vs. Wrist Immobilization for Carpal Tunnel Syndrome". Carpal Tunnel Syndrome (CTS) can be defined as disruption of the median nerve and is characterized by pain, numbness and tingling of the lateral 3.5 digits of the hand. In severe cases, motor function can also be disrupted. There are many factors that can contribute to the development of CTS: inflam...
What is the current status of trial NCT07432750?
This trial is currently recruiting. It is a NA study. The enrollment target is 10 participants. The study started on 2026-03. Estimated completion is 2027-02-28.
What conditions does trial NCT07432750 study?
This clinical trial studies the following conditions: Carpal Tunnel Syndrome (CTS).
What interventions are being tested in trial NCT07432750?
The interventions under investigation include: Osteopathic Manipulative Treatment (PROCEDURE), Wrist Immobilizer (DEVICE).
Who is sponsoring clinical trial NCT07432750?
This trial is sponsored by New York Institute of Technology, which has 49 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT07432750 being conducted?
This trial has 1 study location across New York. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
Learn More About Clinical Trials
Similar trials for Carpal Tunnel Syndrome (CTS)
Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.
Where NCT07432750's enrollment target sits among peer trials
10 1927th of 2000 higher than 26 of 2,000 other NA trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source ClinicalTrials.gov registry export · 2026-08-08
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