Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT07248124

Pilot Study, Aimed at Describing in Myography, the Collapse of the Muscular Response Visualized in the Scratch Collapse Test, in Carpal Tunnel Syndrome.

Led by Elsan · Updated on 2025-11-25

25

Participants Needed

1

Research Sites

26 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The Scratch Collapse Test (SCT) is a neurocutaneous reflex used to detect peripheral nerve compression in nerve tunnel syndromes. It first involves applying a sensory stimulus to the skin over the suspected nerve compression point, then bilaterally testing the strength of a specific muscle in the patient. Compression is then manifested by a transient loss of strength in the muscle on the affected side, while it is preserved on the healthy side. This loss of strength is transient and disappears after a few seconds. This test can be performed during a patient's clinical examination, with the physician assessing strength or, conversely, muscle collapse. However, while several articles have described the relevance of this test, as well as its sensitivity and specificity, no study has specifically investigated and measured this observed loss of eccentric muscle tone and its unilateral and transient nature, even though the phenomenon of CSP (cutaneous silent period) has been described. We therefore propose to analyze the myographic tracing obtained in patients diagnosed with unilateral carpal tunnel syndrome. A transient loss of muscle tone is expected by selective needle myography on the pathological side after cutaneous sensory stimulation of the wrist, while cutaneous sensory stimulation on the healthy side does not alter the tracings obtained by myography.

CONDITIONS

Official Title

Pilot Study, Aimed at Describing in Myography, the Collapse of the Muscular Response Visualized in the Scratch Collapse Test, in Carpal Tunnel Syndrome.

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patient over 18 years old
  • Clinical unilateral carpal tunnel syndrome diagnosed by history, clinical examination, and electromyography
  • Patient who has been informed and has given free, informed, and written consent
  • Patient affiliated with or beneficiary of a social security scheme
Not Eligible

You will not qualify if you...

  • Other associated canal syndromes on either side (ulnar, defilement, lacertus)
  • Rotator cuff pathology, insufficiency, or rupture of the infraspinatus
  • Associated cervical pathology
  • Neuropathy, central or peripheral neurological disease
  • Diabetic patient
  • Cognitive impairments preventing understanding of study information
  • Refusal to participate in the study
  • Pregnant, parturient, or breastfeeding woman
  • Patient under legal protection
  • Patient not receiving health protection
  • Protected patient under guardianship, curatorship, or deprived of liberty by judicial or administrative decision

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Clinique de l'Ormeau

Tarbes, France, 65000

Actively Recruiting

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Research Team

V

Vincent Martinel, Dr

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

OTHER

Number of Arms

1

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