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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03177915
Other study ID # IRB00008406
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date March 2016
Est. completion date February 2017

Study information

Verified date September 2018
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 of 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 February 2017
Est. primary completion date December 2016
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:
Hylase
median nerve hydro-dissection using Hyalase + 10 cc saline injection
Saline
median nerve hydro-dissection using 10 cc saline injection

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 improvement of pain measured by visual analog scale , no pain the scale equal zero , and worst pain the scale equal 10 6 months
Secondary Changes in ultrasound imaging change of cross sectional area in cubic mellimeter 6 months
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