- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04781751
Ultrasonographic Insulin Versus Dexamethasone Injection With Local Anestheticss in Diabetic Patients With Mild to Moderate Median Nerve Entrapement Neuropathy .
March 1, 2021 updated by: Mina Maher, Minia University
Insulin injection in carpal tunnel compared with dexamethsone in diabetic patients
Study Overview
Detailed Description
Trial to decrease median nerve entrapement neuropathy recurrence using insulin co-injection
Study Type
Interventional
Enrollment (Anticipated)
150
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
-
ALMinya, Egypt, 6115
- Recruiting
- Minia University
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
20 years to 70 years (ADULT, OLDER_ADULT)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- All diabetic patients with carpal tunnel syndrome
Exclusion Criteria:
- Refusal to participate
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: TREATMENT
- Allocation: RANDOMIZED
- Interventional Model: PARALLEL
- Masking: DOUBLE
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
NO_INTERVENTION: dexamethasone
dexamethasone with local anesthetics injected for carpal tunnel relief
|
|
ACTIVE_COMPARATOR: Insulin group
insulin with local anesthetics and dexamehtasone injected for carpal tunnel relief
|
Carpal tunnel syndrome sonagraphic injection
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
pain relief
Time Frame: 12 weeks
|
consumption analgesics
|
12 weeks
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (ACTUAL)
February 28, 2021
Primary Completion (ANTICIPATED)
April 5, 2021
Study Completion (ANTICIPATED)
April 30, 2021
Study Registration Dates
First Submitted
February 24, 2021
First Submitted That Met QC Criteria
March 1, 2021
First Posted (ACTUAL)
March 4, 2021
Study Record Updates
Last Update Posted (ACTUAL)
March 4, 2021
Last Update Submitted That Met QC Criteria
March 1, 2021
Last Verified
March 1, 2021
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 212/2-2021
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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