Effect of Curcumin in Adenotonsillectomy pain reductio
Phase 3
Recruiting
- Conditions
- Adenotonsillar hypertrophy.
- Registration Number
- IRCT20130713013976N6
- Lead Sponsor
- Hamedan University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 122
Inclusion Criteria
Patients undergoing Adenotonsillectomy
Age 4 to 12 years of both sexes
Exclusion Criteria
Sensitivity to Turmeric
Using cautery during surgery
In the absence of understanding the pain assessment images by the child and the inability to intervene and lack of parental support
Any known systemic disease, such as congenital anomalies, bleeding disorders, type 1 diabetes, kidney disease, colds, and fever
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Scale of sore throat in the Visual Analog Scale (VAS). Timepoint: Measurement of sore throat in the first 5 days after Adenotonsillectomy. Method of measurement: Visual Analogue Scale.
- Secondary Outcome Measures
Name Time Method The frequency of use of prescribed acetaminophen intake. Timepoint: In the first 5 days after Adenotonsillectomy. Method of measurement: Questionnaire.;Having or not having ear pain (autoelastic). Timepoint: In the first 5 days after Adenotonsillectomy. Method of measurement: Questionnaire.;Tolerate normal diet. Timepoint: In the first 5 days after Adenotonsillectomy. Method of measurement: Questionnaire.;Having or not having nausea. Timepoint: In the first 5 days after Adenotonsillectomy. Method of measurement: Questionnaire.