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Clinical Trials/NCT04346030
NCT04346030
Unknown
Not Applicable

Comparison of Ultrasound-guided Corticosteroid Injection Versus Corticosteroid Injection and Hydrodissection for Carpal Tunnel Syndrome

Taipei Veterans General Hospital, Taiwan1 site in 1 country60 target enrollmentApril 17, 2020

Overview

Phase
Not Applicable
Intervention
Triamcinolone Acetonide
Conditions
Carpal Tunnel Syndrome
Sponsor
Taipei Veterans General Hospital, Taiwan
Enrollment
60
Locations
1
Primary Endpoint
change from baseline in the scores on Boston Carpal tunnel Questionnaire (BQ)
Last Updated
6 years ago

Overview

Brief Summary

The objective of this study is to investigate the effect of ultrasound guided steroid injection versus ultrasound guided steroid hydrodissection to treat patients with CTS.

Detailed Description

This study was a prospective, randomized clinical trial. Patients with CTS were randomly treated with sonographically guided corticosteroid injection (group A); sonographically guided hydrodissection and corticosteroid injection (group B). Boston Carpal tunnel questionnaire, nerve conduction studies and VAS pain score were performed on initial visit and after 6 weeks and 12 weeks .

Registry
clinicaltrials.gov
Start Date
April 17, 2020
End Date
July 2021
Last Updated
6 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Clinical diagnosis of CTS The diagnosis of CTS was confirmed by electrophysiological tests.

Exclusion Criteria

  • presence of thenar atrophy any accompanying orthopedic or neurologic disorders that could mimic CTS such as cervical radiculopathy, polyneuropathy, proximal median nerve entrapment, or thoracic outlet syndrome prior steroid injection into the affected carpal tunnel within 6 months or ever received carpal tunnel surgery history of distal radius fracture pregnancy or lactation regular use of systemic NSAIDs ,corticosteroids or diuretics known allergy to corticosteroids and local anesthetics. impaired cognitive function

Arms & Interventions

steroid and hydrodissection

ultrasound guided steroid injection using 1ml of 10mg triamcinolone acetonide (Shincort) mixed with 1ml of 2% lidocaine hydrochloride (Xylocaine) and 8cc NS

Intervention: Triamcinolone Acetonide

steroid and hydrodissection

ultrasound guided steroid injection using 1ml of 10mg triamcinolone acetonide (Shincort) mixed with 1ml of 2% lidocaine hydrochloride (Xylocaine) and 8cc NS

Intervention: lidocaine hydrochloride

steroid and hydrodissection

ultrasound guided steroid injection using 1ml of 10mg triamcinolone acetonide (Shincort) mixed with 1ml of 2% lidocaine hydrochloride (Xylocaine) and 8cc NS

Intervention: normal saline

steroid only

ultrasound guided steroid injection using 1ml of 10mg triamcinolone acetonide (Shincort) mixed with 1ml of 2% lidocaine hydrochloride (Xylocaine)

Intervention: Triamcinolone Acetonide

steroid only

ultrasound guided steroid injection using 1ml of 10mg triamcinolone acetonide (Shincort) mixed with 1ml of 2% lidocaine hydrochloride (Xylocaine)

Intervention: lidocaine hydrochloride

Outcomes

Primary Outcomes

change from baseline in the scores on Boston Carpal tunnel Questionnaire (BQ)

Time Frame: 0, 6, 12 weeks.

The BQ was interviewed-administered to assess the severity of symptoms and functional status

Secondary Outcomes

  • change from baseline in self reported pain intensity(0, 6, 12 weeks)
  • Change from Baseline in sensory nerve conduction velocity(0, 6, 12 weeks)
  • change from baseline in median nerve distal motor latency(0, 6, 12 weeks)

Study Sites (1)

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