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Not yet recruiting NCT06766370

The Application of Multimodal Ultrasound Imaging in Carpal Tunnel Syndrome

— Observational Carpal Tunnel Syndrome (CTS)

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Ultrasound-guided nerve hydrodissection treatment.
Who it may be relevant to
Registry conditions: Carpal Tunnel Syndrome (CTS). Basic parameters: 18 years — 70 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Center list to be confirmed — check the primary protocol.
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Unsure about the terms? Read our patient guide →

Overview

The aim of this study is to explore the application value of multimodal ultrasound parameters in the diagnosis and treatment follow-up of Carpal Tunnel Syndrome.

Interventions

  • Procedure Ultrasound-guided nerve hydrodissection treatment
    Under ultrasound guidance, a mixed solution of corticosteroids and local anesthetics is injected around the nerve, followed by release of the transverse carpal ligament.

Primary outcome measures

  • Boston Carpal Tunnel Syndrome Questionnaire ，BCTQ [Time frame: 1,3,6,12 months]
Secondary outcome measures (2)
  • the patient's sensory nerve conduction velocity (SNCV) [Time frame: 3,6,12months]
  • the patient's distal motor latency (DML). [Time frame: 3,6,12months]

Eligibility criteria

Inclusion criteria

  • Age between 18 and 70 years;
  • Presence of sensory abnormalities and motor dysfunction in the median nerve distribution area;
  • Positive Tinel's sign or Phalen's test;
  • Neurophysiological examination consistent with mild to moderate Carpal Tunnel Syndrome.-

Exclusion criteria

  • Severe Carpal Tunnel Syndrome;
  • Concurrent rheumatic, metabolic, systemic, or other systemic diseases;
  • Concurrent cervical spondylosis or other peripheral neuropathies;
  • Wrist joint trauma, surgery, space-occupying lesions, or nerve itself with space-occupying lesions;
  • Concurrent malignant tumors or severe cardiopulmonary diseases;
  • History of previous wrist surgery or injections;
  • Pregnancy;
  • Allergy to corticosteroids or local anesthetics.-

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Observational model
Cohort

Study locations

Center list to be confirmed — check the primary protocol.

Identifiers

NCT: NCT06766370 · 2024-796-01

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗