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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05970692
Other study ID # BEU-KTS-01
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date September 26, 2023
Est. completion date December 30, 2024

Study information

Verified date February 2024
Source Dokuz Eylul University
Contact Tülay Çevik Saldiran, PhD
Phone +90 (434) 222 83 32
Email tcsaldiran@beu.edu.tr
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

This study aims to develop Turkish version of the Atroshi-Lyrén 6-item symptoms scale (A-L scale) and to perform validity and reliability evaluations.


Recruitment information / eligibility

Status Recruiting
Enrollment 100
Est. completion date December 30, 2024
Est. primary completion date August 13, 2024
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria: - Aged between 18-65 years old, - Had symptoms of numbness, tingling, weakness and pain in the hands for at least 1 month, - Assessed through provocation tests and physical examination to match the median nerve distribution. Exclusion Criteria: - Not willing to participate in the study, - Clinical or electrophysiological signs of proximal nerve compression, - Diabetes or other metabolic disease, - Rheumatoid arthritis or other general inflammatory diseases.

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
Turkey Bitlis Eren University Bitlis

Sponsors (2)

Lead Sponsor Collaborator
Ilke KARA Bitlis Eren University

Country where clinical trial is conducted

Turkey, 

Outcome

Type Measure Description Time frame Safety issue
Primary Atroshi-Lyrén 6-item symptoms scale The A-L scale consists of 6 items that inquire about severity and frequency of night and daytime numbness and tingling and pain. For each patient the item responses are scored from 1 (best) to5 (worst) and then averaged for the 6 items to yield a total score (only 1 missing item response is allowed) 1 week
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