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Carpal Tunnel Syndrome Evaluation With Ultrasound in Rheumatoid Arthritis Patients

Completed
Conditions
Median Nerve Entrapment
Interventions
Diagnostic Test: Ultarsound
Registration Number
NCT06012630
Lead Sponsor
Burak Tayyip Dede
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.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
90
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,
  • gout,
  • 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.

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Arm && Interventions
GroupInterventionDescription
group:3 Healthy ControlUltarsoundHealthy Control without rheumatologic disease and Carpal tunnel syndrome
group 2: RA with CTSUltarsoundRheumatoid arthritis patients with a diagnosis of CTS based on clinical findings and physical examination
group 1: RA without CTSUltarsoundRheumatoid arthritis patients without a diagnosis of CTS based on clinical findings and physical examination
Primary Outcome Measures
NameTimeMethod
Comparison of US findings among participants6 months

Comparison of US findings among participants

Secondary Outcome Measures
NameTimeMethod
Relationship between US findings and disease activity in the patient group6 months

The correlation between the US findings of the participants in the patient group and the CDA, which evaluates disease activity, was examined.

Trial Locations

Locations (1)

Istanbul Training and Resarch Hospital

🇹🇷

Istanbul, Turkey

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