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Clinical Trials/NCT06012630
NCT06012630
Completed
Not Applicable

Ultrasound Evaluation of the Median Nerve in Patients With Rheumatoid Arthritis and Its Relationship With Disease Activity

Burak Tayyip Dede1 site in 1 country90 target enrollmentJanuary 15, 2023

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Median Nerve Entrapment
Sponsor
Burak Tayyip Dede
Enrollment
90
Locations
1
Primary Endpoint
Comparison of US findings among participants
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

In rheumatoid arthritis (RA) patients, the diagnosis of Carpal tunnel syndrome (CTS) was made based on clinical findings and physical examinations. Then, the cross-sectional areas of the participants' median nerves from different levels were measured. Meidolateral and anteroposterior diameter were measured at the level of the carpal tunnel inlet. Flattening ratio was calculated. wrist to forearm ratio and wrist to forearm difference were calculated. The obtained data were compared between RA with CTS, RA without CTS and healthy control.

Registry
clinicaltrials.gov
Start Date
January 15, 2023
End Date
August 15, 2023
Last Updated
2 years ago
Study Type
Observational
Sex
All

Investigators

Sponsor
Burak Tayyip Dede
Responsible Party
Sponsor Investigator
Principal Investigator

Burak Tayyip Dede

Physical Medicine and Rehabilitation

Istanbul Training and Research Hospital

Eligibility Criteria

Inclusion Criteria

  • RA patients identified according to the 2010 American College of Rheumatology/Europan Leage Against Rheumatism classification criteria
  • healthy controls (HC) with no history of rheumatic diseases and CTS.
  • Individuals aged 18-65 years.

Exclusion Criteria

  • thoese with hypothyroidism,
  • diabetes mellitus,
  • history of CTS surgery,
  • upper extremity plexopathy,
  • polinöropathy,
  • uncontrollable fibromyalgia,
  • steroid injection for CTS
  • For the HC group, those with phalen or tinnel detected in at least one wrist and those with bifid median nerve detected during US evaluation were not included in the study.

Outcomes

Primary Outcomes

Comparison of US findings among participants

Time Frame: 6 months

Comparison of US findings among participants

Secondary Outcomes

  • Relationship between US findings and disease activity in the patient group(6 months)

Study Sites (1)

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