Carpal Tunnel Syndrome Evaluation With Ultrasound in Rheumatoid Arthritis Patients

NCT ID: NCT06012630

Last Updated: 2023-08-25

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

COMPLETED

Total Enrollment

90 participants

Study Classification

OBSERVATIONAL

Study Start Date

2023-01-15

Study Completion Date

2023-08-15

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

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

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Median Nerve Entrapment

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Observational Model Type

COHORT

Study Time Perspective

CROSS_SECTIONAL

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

group 1: RA without CTS

Rheumatoid arthritis patients without a diagnosis of CTS based on clinical findings and physical examination

Ultarsound

Intervention Type DIAGNOSTIC_TEST

Median nerve evaluation of participants with ultrasound

group 2: RA with CTS

Rheumatoid arthritis patients with a diagnosis of CTS based on clinical findings and physical examination

Ultarsound

Intervention Type DIAGNOSTIC_TEST

Median nerve evaluation of participants with ultrasound

group:3 Healthy Control

Healthy Control without rheumatologic disease and Carpal tunnel syndrome

Ultarsound

Intervention Type DIAGNOSTIC_TEST

Median nerve evaluation of participants with ultrasound

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

Ultarsound

Median nerve evaluation of participants with ultrasound

Intervention Type DIAGNOSTIC_TEST

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

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.
Minimum Eligible Age

18 Years

Maximum Eligible Age

65 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

Burak Tayyip Dede

OTHER_GOV

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Burak Tayyip Dede

Physical Medicine and Rehabilitation

Responsibility Role SPONSOR_INVESTIGATOR

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

Istanbul Training and Resarch Hospital

Istanbul, , Turkey (Türkiye)

Site Status

Countries

Review the countries where the study has at least one active or historical site.

Turkey (Türkiye)

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

22/04/2022; 2011-KAEK-50;126

Identifier Type: -

Identifier Source: org_study_id

More Related Trials

Additional clinical trials that may be relevant based on similarity analysis.

Thenar Muscle Ultrasound in CTS Evaluation
NCT06730724 NOT_YET_RECRUITING