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Main
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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register. |
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Register:
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ClinicalTrials.gov |
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Last refreshed on:
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17 May 2016 |
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Main ID: |
NCT02766114 |
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Date of registration:
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04/05/2016 |
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Prospective Registration:
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No |
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Primary sponsor: |
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Public title:
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Carpal Tunnel Release Through Mini Transverse Approach
CTRMTA |
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Scientific title:
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Carpal Tunnel Release Through Mini Transverse Approach |
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Date of first enrolment:
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February 2013 |
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Target sample size:
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43 |
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Recruitment status: |
Completed |
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URL:
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https://clinicaltrials.gov/show/NCT02766114 |
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Study type:
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Interventional |
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Study design:
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Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment
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Phase:
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N/A
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Countries of recruitment
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Syrian Arab Republic
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Key inclusion & exclusion criteria
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Inclusion Criteria:
- Patients presented with Carpal Tunnel Syndrome refractory to conservative treatment
- Participant cooperation sufficient to operate under local anesthesia
Exclusion Criteria:
- Un controlled diabetes mellitus type 1 and 2
- Patients with non controlled Vascular hypertension
- Significant renal disease, defined as a history of chronic renal failure requiring
dialysis or kidney transplant.
- Myocardial infarction, other acute cardiac event requiring hospitalization, stroke,
transient ischemic attack, or treatment for acute congestive heart failure within 4
months prior to randomization
- Patients with history of Carpal Tunnel release surgery failure
Age minimum:
16 Years
Age maximum:
70 Years
Gender:
Both
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Health Condition(s) or Problem(s) studied
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Carpal Tunnel Release
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Carpal Tunnel Transverse Approach
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Carpal Tunnel Syndrome
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CTS
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Carpal Tunnel Surgery
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Intervention(s)
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Procedure: Carpal tunnel release through Mini Transverse Approach
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Primary Outcome(s)
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Proportion of patients with post surgical trauma
[Time Frame: Up to eight weeks]
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Secondary Outcome(s)
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Proportion of patients with cosmetic scar
[Time Frame: Up to 6 months]
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Duration of rehabilitation period
[Time Frame: Up to three weeks]
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Secondary ID(s)
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Sayed Issa's Approach
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Source(s) of Monetary Support
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Please refer to primary and secondary sponsors
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Results
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Results available:
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Date Posted:
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Date Completed:
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URL:
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