Actively Recruiting
Added Value of Ultrasonography in the Diagnosis, Management, and Follow-Up of Carpal Tunnel Syndrome
Led by Kafrelsheikh University · Updated on 2025-02-20
60
Participants Needed
1
Research Sites
N/A
Total Duration
On this page
AI-Summary
What this Trial Is About
Carpal tunnel syndrome (CTS) is a common nerve compression disorder affecting the wrist, caused by pressure on the median nerve within the carpal tunnel. Researchers are evaluating the use of ultrasound (US) and nerve conduction studies (NCS) as tools to help diagnose CTS, plan treatment, and monitor patients over time. This study focuses on how ultrasound can assist in understanding nerve changes and anatomical variations related to CTS. Participants will undergo high-resolution, real-time ultrasound imaging of both wrists using a 12 MHz linear array transducer. The ultrasound examinations will take place before surgery and again three months after surgery. This imaging approach aims to measure various nerve parameters such as size, blood flow, and movement, offering a non-invasive and quick method to support diagnosis and follow-up. During the study, patients will receive ultrasound assessments at specified times and clinical evaluations for CTS. Researchers will measure the sensitivity of ultrasound in diagnosing CTS during surgery. The study involves monitoring changes in the median nerve and surrounding structures to help improve diagnosis and management. Participation includes imaging visits and clinical follow-up over a period encompassing pre- and post-surgical assessments.
CONDITIONS
Brief Title
Added Value of Ultrasonography in the Diagnosis, Management, and Follow-Up of Carpal Tunnel Syndrome
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age 18 years or older
- Both sexes
- Patients diagnosed with carpal tunnel syndrome
You will not qualify if you...
- History of wrist surgery, including carpal tunnel injection, or wrist fracture
- Clinical or electrophysiological evidence of conditions mimicking carpal tunnel syndrome such as proximal median neuropathy, cervical radiculopathy, or polyneuropathy
- History of underlying disorders related to carpal tunnel syndrome including diabetes mellitus, rheumatoid arthritis, pregnancy, acromegaly, or hypothyroidism
- Electrodiagnostic findings suggesting other neurological disorders
- Presence of subclinical sensory polyneuropathy
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
Duration - Up to 1 day
Participants undergo high-resolution real-time ultrasound examination of the carpal tunnel (both hands) to assess median nerve parameters and anatomical variations.
1 visit (in-person)
Duration - 3 months
Participants are monitored over time with a follow-up ultrasound examination performed 3 months after surgery to assess changes in the median nerve and surrounding structures.
1 follow-up visit (in-person)
Trial Site Locations
Total: 1 location
1
Kafrelsheikh University
Kafr ash Shaykh, Kafrelsheikh, Egypt, 33516
Actively Recruiting
Research Team
A
Ahmed A Zahra, MD
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
Similar Trials
Frequently Asked Questions
Have more questions? Get in touch with our team for quick support
Not the Right Trial for You?
Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.
Already have an account? Log in here