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NCT05725460 Clinical Trial

Ultrasound Guided Median Nerve Hydrodissection Using Dextrose

Carpal Tunnel Syndrome Clinical Trial

Official title:
Efficacy of Dextrose 5% in Comparison With Steroid in Median Nerve Ultrasound Guided Hydrodissection in Patients With Carpal Tunnel Syndrome

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT05725460
Other study ID # iraqiboard
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date February 1, 2023
Est. completion date September 13, 2023

Study information
Verified date May 2023
Source Iraqi Board of medical specialties
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

to compare the efficacy of dextrose 5% with steroid hydrodissection in patients with carpal tunnel syndrome

Description:

in some cases there is prohibition to use steroid with example the patient rejection to use steroid the maneuver planned median nerve hydrodissection using ultrasound and 10 mld of dextrose 5%, unleash the median nerve for the surrounding structure and short follow up planned to be 2 weeks

Recruitment information / eligibility
Status Completed
Enrollment 40
Est. completion date September 13, 2023
Est. primary completion date August 23, 2023
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 20 Years to 75 Years
Eligibility Inclusion Criteria: severe carpal tunnel syndrome failed medical management - Exclusion Criteria: previous failed surgery previous failed injection previous failed trial of hydrodissection cervical or brachial nerve entrapment wrist osteoarthritis or rheumatoid pregnant diabetes mellitus -

Study Design

Related Conditions & MeSH terms

Intervention

Procedure:
• dextrose 5% median nerve hydrodissection
planned to be a good alternative to steroid hydrodissection

Locations
Country Name City State
Iraq Baghdad Medical City Baghdad

Sponsors (1)
Lead Sponsor Collaborator
Iraqi Board of medical specialties

Country where clinical trial is conducted

Iraq, 

Outcome
Type Measure Description Time frame Safety issue
Primary pain relief in 2 weeks follow up difference in sensory and functional symptoms post median nerve hydrodissection using dextrose and compare this effect with steroid population arm using Boston questionnaire 6 months
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