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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05624866
Other study ID # 17200681
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date October 10, 2022
Est. completion date December 10, 2023

Study information

Verified date November 2022
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 mononeuropathy due to entrapment of the median nerve in the carpal tunnel. a lot of modalities are available for treatment of mild to moderate CTS.


Description:

Carpal tunnel syndrome (CTS) is a common mononeuropathy due to entrapment of the median nerve in the carpal tunnel. a lot of modaleties are available for treatment of mild to moderate CTS. In case of failed conservative oral therapey, local hydro-dessction of the median nerve can be done with saline alone. local anethetics, steroids, hyalase,and ozone have been utilized to augment the symptoms reliefe. Dexmeditomidine (DEX) has been studied as adjuvant for nerve block to aumnet the pain reliefe. Recently, it has been discovered that DEX can offer some antinflammatory effects when injected in the perineural area. Upon such discovery, the goal of this study has been built.


Recruitment information / eligibility

Status Recruiting
Enrollment 60
Est. completion date December 10, 2023
Est. primary completion date November 10, 2023
Accepts healthy volunteers No
Gender All
Age group 20 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 - allergy to utilized drugs - diabetic - previous surgery in the site of injection - previous injection in the targeted site within the last year

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Dexmedetomidine
injection of 1 microgram/kg dexmeditomidine + 10 cc saline injection nearby median nerve as hydro-dissection
Triamcinolone
injection of 40 mg triamcinolone + 10 cc saline injection nearby median nerve as hydro-dissection

Locations

Country Name City State
Egypt Assiut Universit Hospital 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 visual analoge scale visual analog scale of pain value of (0 cm) no pain , and value of (10 cm) worst pain visual analog scale of pain value of (0 cm) no pain , and value of (10 cm) worst pain 6 months
Secondary change of cross sectional area of the median nerve change of cross sectional area of the median nerve mm2 6 months
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