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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05280223
Other study ID # IRB0002022
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date April 1, 2022
Est. completion date August 25, 2023

Study information

Verified date October 2023
Source Assiut University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Carpal tunnel syndrome (CTS) is a common peripheral entrapment neuropathy, this study aims to investigate if, and to what extent hydro-dissection hyalase and saline versus dexmedetomidine upon the median nerve could offer symptoms and clinical improvement


Description:

Carpal tunnel syndrome (CTS) is the most common compression syndrome the upper extremities. Its problem has a high prevalence ranged estimated prevalence of 3.8% in the general population, 3 and 7.8% in the working population. It occurs at any age, especially in individuals in their 40s to 60s, and the male: female ratio is reported to be 3:7. A lot of treatment modalities have been tried to improve the condition, starting from local anesthetic injection, steroid, and up to surgical decompression of the nerves.


Recruitment information / eligibility

Status Completed
Enrollment 60
Est. completion date August 25, 2023
Est. primary completion date June 30, 2023
Accepts healthy volunteers No
Gender All
Age group 18 Years to 60 Years
Eligibility Inclusion Criteria: - adult patients - complaining of carpal tunnel syndrome of 3 month duration or more - diagnosed axonal neuropathy using electrodiagnosis , nerve conduction study Exclusion Criteria: - • patient refusal infection at the site of intervention - local anesthetic allergy

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Dexmedetomidine
injection of 1 microgram/kg dexmeditomidine + 10 cc saline injection nearby median nerve as hydrodissection
Hyalase
injection of Hyalase + 10 cc saline injection nearby median nerve as hydro-dissection

Locations

Country Name City State
Egypt Emad Zarief Kamel Said Assiut

Sponsors (1)

Lead Sponsor Collaborator
Assiut University

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Primary Pain alleviation pain alleviation improvement of pain measured by visual analog scale , no pain the scale equal zero , and worst pain the scale equal 10 6 months
Secondary Median nerve cross sectional area Changes in ultrasound imaging change of cross sectional area in cubic mellimeter 6 months
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