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Completed NCT07656831

Study Comparing Harmonic Scalpel and Conventional Cold Steel Tonsil Removal Surgery in Children Requiring Tonsillectomy

Conditions: Chronic Tonsillitis

Sex: All
Ages: 5 Years – 45 Years
Healthy volunteers: No
Phase: NA
Enrollment: 66
Sponsor: Allama Iqbal Teaching Hospital

Location: Allama Iqbal Teaching Hospital Dera Ghazi Khan Punjab Province

Summary

This clinical trial aims to compare two commonly used methods of tonsil removal surgery (tonsillectomy) in children and adults with chronic tonsillitis. Chronic tonsillitis refers to repeated episodes of tonsil infection that occur frequently over several years and require surgical removal of the tonsils. The main question this study aims to answer is: Does tonsillectomy performed with a harmonic scalpel result in less pain three days after surgery compared with the conventional cold steel dissection technique? Researchers will also compare: How long the surgery takes to perform How much blood is lost during the operation The level of pain experienced three days after surgery A total of 66 participants aged 5 to 45 years who are scheduled for tonsillectomy because of chronic tonsillitis will take part in the study. Participants will be randomly assigned to undergo either conventional cold steel dissection tonsillectomy or harmonic scalpel tonsillectomy. All surgeries will be performed by experienced ENT surgeons following standard hospital procedures. After surgery, participants will receive routine medications and instructions for home care. They will be followed for three days and then return to the ENT clinic for assessment of pain and examination of the healing of the surgical site. The study hypothesis is that patients undergoing harmonic scalpel tonsillectomy will experience less pain three days after surgery than those undergoing conventional cold steel dissection tonsillectomy.

Eligibility Criteria

Inclusion Criteria: * chronic tonsillitis and planned for tonsillectomy Exclusion Criteria: * Upper respiratory tract infection within preceding three weeks * Peritonsillar abscess or history of quinsy * Known bleeding disorder (hemophilia, thrombocytopenia) or on anticoagulant therapy * Craniofacial anomalies or syndromic conditions affecting airway or surgical anatomy * Uncontrolled diabetes, severe cardiopulmonary disease

Interested in this study? View the official listing for contact and enrollment details.

View on ClinicalTrials.gov

Source: ClinicalTrials.gov (NCT07656831). StuddyBuddy aggregates publicly available trial information.