Efficiency of Tonsillectomy Bipolar Resection device in tonsillectomy
Not Applicable
- Conditions
- Tonsillectomy.
- Registration Number
- IRCT20190106042251N1
- Lead Sponsor
- Shiraz University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 76
Inclusion Criteria
Having satisfaction with the study
Getting the consent and full cooperation of the parents of children
The need for performing Tonsillectomy
Staying in Shiraz
Children in the age range of 5 to 15 years
Exclusion Criteria
Preoperative infection
Having bleeding diseases
Disturbances in coagulation tests (PLT, PT, PTT, INR)
Having a mental retardation
Chronic underlying diseases (diabetes, cancer, etc.)
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method ser-friendly device. Timepoint: Immediately after the intervention. Method of measurement: Davis & Venkatesh technology acceptance questionnaire.;The amount of bleeding during and after surgery. Timepoint: During the intervention, 1, 3 and 7 days after the intervention. Method of measurement: Subtracting the weight of blood-stained gauzes from the weight of surgical gauzes.
- Secondary Outcome Measures
Name Time Method Mortality. Timepoint: 1, 3 and 7 days after the intervention. Method of measurement: Percentage of deaths in a month.