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Thenar Muscle Ultrasound in CTS Evaluation

NCT ID: NCT06730724

Last Updated: 2024-12-12

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

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Recruitment Status

NOT_YET_RECRUITING

Total Enrollment

40 participants

Study Classification

OBSERVATIONAL

Study Start Date

2024-12-10

Study Completion Date

2025-01-10

Brief Summary

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This study will include 20 patients aged 18-75 years who have been diagnosed with carpal tunnel syndrome (CTS) based on electrophysiological examinations performed within the last three months, as well as 20 healthy volunteers without a CTS diagnosis. Sociodemographic data such as age, gender, height, weight, and BMI will be recorded. Pinch grip strength will be evaluated using a Jamar pinch meter, and hand grip strength will be assessed using a Jamar dynamometer. Ultrasound will be used to measure the cross-sectional area and thickness of the thenar muscles as well as the cross-sectional area of the median nerve. Additionally, previous electrophysiological examination results will be recorded for the CTS patients.

Detailed Description

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Conditions

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Carpal Tunnel Syndrome

Study Design

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Observational Model Type

CASE_CONTROL

Study Time Perspective

CROSS_SECTIONAL

Study Groups

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Carpal tunnel syndrome

Patients with carpal tunnel syndrome

No intervention

Intervention Type OTHER

No intervention

Control group

Healthy controls without carpal tunnel syndrome

No intervention

Intervention Type OTHER

No intervention

Interventions

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No intervention

No intervention

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Patients aged 18-75 years.
* Diagnosed with carpal tunnel syndrome based on electrophysiological examination within the last 3 months.
* Healthy volunteers without a diagnosis of carpal tunnel syndrome.
* Volunteered to participate in the study.

Exclusion Criteria

* Refusal to participate in the study.
* History of surgery due to carpal tunnel syndrome.
* Presence of neuromuscular diseases.
* Presence of advanced osteoarthritis.
* Presence of psychiatric disorders.
* Presence of cognitive impairments that may hinder study participation.
Minimum Eligible Age

18 Years

Maximum Eligible Age

75 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Beylikduzu State Hospital

OTHER

Sponsor Role lead

Responsible Party

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Busra Sirin

Principle Investigator

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Büşra Şirin Ahısha

Role: PRINCIPAL_INVESTIGATOR

Beylikdüzü State Hospital

Locations

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Beylikdüzü State Hospital

Istanbul, Beylikdüzü, Turkey (Türkiye)

Site Status

Countries

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Turkey (Türkiye)

Central Contacts

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Büşra Şirin Ahısha, MD

Role: CONTACT

Phone: 02124443322

Email: [email protected]

Other Identifiers

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BeylikduzuStateH12

Identifier Type: -

Identifier Source: org_study_id