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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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15 February 2016 |
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Main ID: |
NCT02285491 |
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Date of registration:
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05/11/2014 |
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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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Local Anesthetic Injection Into Both Angles of the Rectus Sheath Incision
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Scientific title:
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Efficacy of Local Anesthetic Injection Into Both Angles of the Rectus Sheath Incision for Postoperative Cesarean Delivery Analgesia. |
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Date of first enrolment:
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November 2014 |
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Target sample size:
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225 |
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Recruitment status: |
Completed |
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URL:
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https://clinicaltrials.gov/show/NCT02285491 |
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Study type:
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Interventional |
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Study design:
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Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Investigator, Outcomes Assessor), Primary Purpose: Treatment
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Phase:
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Phase 0
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Countries of recruitment
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Egypt
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Key inclusion & exclusion criteria
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Inclusion Criteria:
- patients booked for lscs
- primisection
- singleton pregnancy
Exclusion Criteria:
- emergency cesarean section
- bleeding tendency
- hypersensitivity to local anesthetic
Age minimum:
20 Years
Age maximum:
40 Years
Gender:
Female
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Health Condition(s) or Problem(s) studied
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Postoperative Cesarean Delivery Pain
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Intervention(s)
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Drug: 10ml of bupivacaine 0.5%
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Drug: Placebo
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Primary Outcome(s)
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Pain assessment during rest and ambulation by visual analogue scale
[Time Frame: for 24 hours after lscs]
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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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