Ireland
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Active, not recruiting Observational

Ultrasound-based Artificial Intelligence for Classification of Carpal Tunnel Syndrome

NCT06697392 · tracked via the Priya Life Science China tracker
Phase
Observational
Started
2024-11-15
Last updated
2024-11-20

Condition(s) studied

Carpal Tunnel Syndrome (CTS)UltrasoundArtificial Intelligence (AI)

Investigational drug(s) / intervention(s)

ultrasound examination

ultrasound examination: The investigators intend to perform ultrasound examinations for the participants with CTS.

Study summary

Carpal tunnel syndrome (CTS) is one of the most prevalent peripheral neuropathies, impacting approximately 4% of the general population. It is typically classified into three degrees: mild, moderate, and severe. Accurate grading of carpal tunnel syndrome (CTS) is essential for determining appropriate treatment options, thereby playing a crucial role in optimizing patient outcomes. Electrophysiological testing (EST) is a key parameter for grading carpal tunnel syndrome (CTS). However, it is limited by several factors, including its invasive nature, poor reproducibility, and reduced sensitivity for detecting early-stage disease. Recently, ultrasound has gained widespread acceptance among clinicians for the assessment and grading of CTS. Nonetheless, radiologists often encounter challenges in this process due to the variability in image quality, differences in experience, and inherent subjectivity.

To address these issues, artificial intelligence presents a promising solution. Therefore, this study aims to develop a deep learning model for grading CTS by leveraging multimodal imaging features, including B-mode ultrasound, superb microvascular imaging (SMI), and elastography. Additionally, the investigators intend to validate the model's effectiveness by testing it with images from various clinical centers, ensuring its generalizability across different clinical settings.

Eligibility

Sex
ALL
Min age
18 Years
Max age
80 Years
Healthy volunteers
No
Inclusion Criteria: * those who have complained about associated symptoms about CTS, including pain, numbness, and weakness of hand. * those who perform ultrasound examinations of median nerve within 1 week of the symptom. * those who have electrophysilogical test results as reference standard. Exclusion Criteria: * those who had a surgery in the affected hand. * those who had a trauma or fracture in the affected hand. * those who had rheumatoid-related conditions, autoimmune diseases, and endocrine disorders.

Primary outcome measure(s)

  • grading of CTS — baseline

Trial sites (1)

FacilityCityRegionStatus
Peking University People's Hospital Beijing Beijing. PR
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06697392 on ClinicalTrials.gov ↗ ← All trials in China