Compare the Effect of Radiofrequency (TECAR) and Ultrasound on Sensation, Hand Dexterity, and Quality of Life in Patients With Carpal Tunnel Syndrome.
NCT07700316
Carpal Tunnel Syndrome, Carpal Tunnel Syndrome (CTS)
Gamasa, Egypt
View Trial DetailsNCT Number: NCT07699289
The goal of this observational study is to evaluate skin temperature patterns measured by infrared thermography in patients with carpal tunnel syndrome (CTS). The main questions it aims to answer are: Are skin temperature patterns associated with CTS as determined by 6-item CTS scale?
Participants diagnosed with CTS as part of their routine clinical care will undergo infrared thermal imaging and electrodiagnostic evaluation according to the study protocol. The relationship between thermographic findings and electrodiagnostic severity will be analyzed.
Trial opening soon.
Get Notified18 year and older
All sexes
Observational
Methods
Submit the study protocol for approval by the Human Research Ethics Committee of Ramathibodi Hospital.
Recruit eligible participants, including both cases and controls, who meet the predefined inclusion and exclusion criteria.
Explain the study objectives and procedures to all potential participants. Written informed consent will be obtained from all participants before enrollment.
Digital infrared thermography of both hands will be performed according to the following standardized procedure:
A physician will perform history taking, physical examination, and assessment using the CTS-6 scale. The following information will be collected:
Skin temperature will be measured from thermographic images at the first, second, and third fingertips, the thenar eminence, and the hypothenar eminence. Thermographic parameters will subsequently be calculated according to the method described by Park et al.
Electrodiagnostic findings of the index hand will be retrieved from medical records if the examination was performed as part of routine clinical care. The following information will be collected:
Electrodiagnostic findings will not be used to determine participant eligibility or establish the diagnosis. Diagnostic accuracy analyses will be performed using the CTS-6 as the primary reference standard.
Statistical analyses will be performed to determine the diagnostic performance of infrared thermography.
Study findings will be analyzed and reported.
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Time frame: at the Enrollment
Diagnostic value of Digital Infrared Thermographic in diagnosis of CTS
Contact information is provided by the study sponsor or research team.
Mahidol University
Other
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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