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. |
Register:
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ClinicalTrials.gov |
Last refreshed on:
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13 June 2023 |
Main ID: |
NCT02291705 |
Date of registration:
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07/11/2014 |
Prospective Registration:
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No |
Primary sponsor: |
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Public title:
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Ultrasound-guided Rectus Sheath Block In Children
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Scientific title:
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Date of first enrolment:
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January 2012 |
Target sample size:
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40 |
Recruitment status: |
Completed |
URL:
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https://clinicaltrials.gov/show/NCT02291705 |
Study type:
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Interventional |
Study design:
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Allocation: Randomized. Intervention model: Parallel Assignment. Primary purpose: Treatment. Masking: Single (Outcomes Assessor).
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Phase:
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Phase 4
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Countries of recruitment
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Turkey
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Contacts
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Name:
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dilek ozcengiz, MD |
Address:
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Telephone:
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Email:
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Affiliation:
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CUKUROVA UNIVERSITY |
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Key inclusion & exclusion criteria
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Inclusion Criteria:
- The children aged 2-7 years scheduled for inguinal hernia repair
Exclusion Criteria:
- American Society of Anesthesiologists (ASA) classification III or greater, history of
long term analgesic use, use of any analgesic within 24 hours before surgery, bleeding
disorder, infection of application area, ultrasound imaging was inadequate and
inability of the FLACC pain scoring system, substance sensitivity to local
anesthetics.
Age minimum:
2 Years
Age maximum:
7 Years
Gender:
All
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Health Condition(s) or Problem(s) studied
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Postoperative Pain
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Intervention(s)
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Drug: Tramadol
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Procedure: rectus sheath block
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Primary Outcome(s)
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Pain Scores
[Time Frame: postoperative 24 hours]
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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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