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The comparision of two methods of tonsillectomy convensional and harmonic

Phase 3
Conditions
Chronic tonsillitis.
J35.1 Hypertrophy of tonsils Enlargement of tonsils
Registration Number
IRCT201609179039N4
Lead Sponsor
Vice Chancellorfor Research, School of Medicine,Tehran University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
32
Inclusion Criteria

Tonsillar hypertrophy; recurrent tonsillitis
Exclusion criteria: Histiry of coagulopathy or anticoagulant therapy; past tonsillectomy; speech disorder; mental and developmental disorders

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Surgery time. Timepoint: from incision to end of hemostasis of the same side. Method of measurement: Cronometer.;The volume of intraoperative bleeding. Timepoint: from incision to end of hemostasis of the same side. Method of measurement: Measuring the suction bottle and weightening of bloody gazes.
Secondary Outcome Measures
NameTimeMethod
Postoperative bleeding. Timepoint: after operation. Method of measurement: Bleeding or no bleeding after surgery.;Postoperative pain. Timepoint: first and seventh days after surgery. Method of measurement: Pain scale scoring system.
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