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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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31 August 2015 |
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Main ID: |
NCT02355678 |
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Date of registration:
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26/01/2015 |
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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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Dexamethasone Versus Local Infiltration Technique for Tonsillectomy in Children
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Scientific title:
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The Effect of Dexamethasone Versus Local Infiltration Technique on Postoperative Nausea and Vomiting After Tonsillectomy in Children: A Randomized Double-blind Clinical Trial |
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Date of first enrolment:
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January 2015 |
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Target sample size:
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129 |
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Recruitment status: |
Completed |
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URL:
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https://clinicaltrials.gov/show/NCT02355678 |
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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, Masking: Double Blind (Subject, Caregiver, Investigator), 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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Lebanon
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Key inclusion & exclusion criteria
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Inclusion Criteria:
Patients scheduled for total or partial tonsillectomy with or without adenoidectomy
Exclusion Criteria:
Patients who received antiemetics, steroids, antihistaminics, or psychoactive drugs within
24 hours before surgery.
Patients who are suspected to have malignant neoplasm and signs of acute pharyngeal
infection..
Patients who have asthma, diabetes mellitus, bleeding problems, and allergy towards
bupivacaine.
Age minimum:
2 Years
Age maximum:
13 Years
Gender:
Both
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Health Condition(s) or Problem(s) studied
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Postoperative Nausea and Vomiting
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Intervention(s)
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Drug: dexamethasone
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Drug: General anesthesia
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Drug: Propacetamol hydrochloride
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Drug: Tramadol hydrochloride
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Procedure: gastric content suction
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Drug: Local anesthetic infiltration
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Drug: Paracetamol Suppository
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Procedure: Tonsillectomy
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Primary Outcome(s)
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Incidence of postoperative nausea and vomiting
[Time Frame: 5 postoperative days]
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Secondary Outcome(s)
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Postoperative pain
[Time Frame: 5 postoperative days]
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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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