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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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16 December 2017 |
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Main ID: |
NCT03260439 |
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Date of registration:
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18/08/2017 |
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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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Tramadol in Penial Block Does it Improve Efficiency of Postoperative Analgesia in Circumcision
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Scientific title:
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Doses Tramadol With Bupivacaine in Penial Block Improve Efficiency of Postoperative Analgésia in Children in Circumcision |
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Date of first enrolment:
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June 2014 |
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Target sample size:
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106 |
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Recruitment status: |
Completed |
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URL:
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https://clinicaltrials.gov/show/NCT03260439 |
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Study type:
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Interventional |
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Study design:
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Allocation: Randomized. Intervention model: Parallel Assignment. Primary purpose: Other. Masking: Triple (Participant, Investigator, Outcomes Assessor).
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Phase:
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N/A
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Countries of recruitment
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Tunisia
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Contacts
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Name:
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leila Mansali Stambouli, MD PhD |
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Address:
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Telephone:
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Email:
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Affiliation:
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University Hospital of Fattouma Bourguiba Monastir TUNISIA |
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Key inclusion & exclusion criteria
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Inclusion Criteria:
- ASA physical status I or II
- Were scheudled to circumcision surgery
- Performed by experenced surgeon under general anesthesia
Exclusion Criteria:
- children with full stomach
- A history of gastric reflux
- A history of cardiovascular or neuromuscular disease
- Allergies to the study drugs
Age minimum:
1 Year
Age maximum:
8 Years
Gender:
All
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Health Condition(s) or Problem(s) studied
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Tramadol - Anesthetics- Child - Circumcision
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Intervention(s)
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Drug: Tramadol
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Drug: Placebo
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Primary Outcome(s)
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Postoperative analgesia
[Time Frame: from awake until 60 min after emergence]
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Secondary ID(s)
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OMB NO: 0925-0586
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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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