RECRUITING

Pilot Study Evaluating the Elasticity and Shear Wave Modulus (Stiffness) of the Median Nerve in Patients With Mild to Moderate Idiopathic Carpal Tunnel Syndrome Receiving OMT and Conservative Therapy

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Conditions

Carpal Tunnel Syndrome

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Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

To evaluate and quantify changes in the elasticity and shear wave modulus (stiffness) of the median nerve in patients diagnosed with mild to moderate carpal tunnel syndrome following osteopathic manipulative therapy.

Official Title

Pilot Study Evaluating the Elasticity and Shear Wave Modulus (Stiffness) of the Median Nerve in Patients With Mild to Moderate Idiopathic Carpal Tunnel Syndrome Receiving OMT and Conservative Therapy

Quick Facts

Study Start:2024-02-26
Study Completion:2025-09-01
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06150443

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years to 65 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Diagnosis of unilateral or bilateral mild to moderate carpal tunnel syndrome, based on recent EMG findings
  1. * History of undergoing recent physical therapy for treatment of carpal tunnel syndrome
  2. * History of wrist trauma or surgery
  3. * Hypothyroidism
  4. * Severe CTS that has progressed to muscle atrophy
  5. * Systemic disease or condition including but not limited to diabetes mellitus, thyroid disorders, rheumatoid disorders, Paget's bone disease, gout, myxedema, multiple myeloma, acromegaly, hepatic disease, dialysis patients, or other diseases or conditions in which peripheral neuropathies are common.
  6. * Secondary cause of CTS such as a ganglion cyst, mass, or an accessory muscle shown by US or MRI of the affected wrist.
  7. * Bifid median nerve as shown by US or MRI of the affected wrist
  8. * pregnant or recently postpartum

Contacts and Locations

Study Contact

Roland Gazaille, DO
CONTACT
937-297-6307
roland.gazaille@ketteringhealth.org

Principal Investigator

Roland Gazaille, DO
PRINCIPAL_INVESTIGATOR
Kettering Health

Study Locations (Sites)

Kettering Health
Dayton, Ohio, 45458
United States

Collaborators and Investigators

Sponsor: Kettering Health Network

  • Roland Gazaille, DO, PRINCIPAL_INVESTIGATOR, Kettering Health

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2024-02-26
Study Completion Date2025-09-01

Study Record Updates

Study Start Date2024-02-26
Study Completion Date2025-09-01

Terms related to this study

Additional Relevant MeSH Terms

  • Carpal Tunnel Syndrome