Which tonsil surgery tool hurts less? new study aims to find out
NCT ID NCT07265531
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study compares two common surgical tools (monopolar and bipolar electrocautery) used during tonsil removal to see which one causes less pain and bleeding after surgery. It involves 74 people aged 5 to 40 who need their tonsils out due to chronic tonsillitis or other issues. Researchers will measure pain levels and any bleeding in the days following the procedure.
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Study facts
What this study's own registry entry says, in plain language.
- Participants
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About 74 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Jul 2025
- Expected to finish
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Jul 2026
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
The frequent patients are children
- Ages
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5 to 17 years
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria * Patients aged between 5 and 40 years. * Indicated for elective tonsillectomy due to recurrent tonsillitis, obstructive sleep apnea, or chronic tonsillar hypertrophy. * Medically stable to undergo general anesthesia and surgical procedure. * Ability to understand and provide informed consent (or parental/guardian consent for minors). * Willing to complyy with study procedures and follow-up schedule. Exclusion Criteria * History of bleeding disorders (e.g., hemophilia, thrombocytopenia). * Use of anticoagulants or antiplatelet therapy within 7 days prior to surgery. * Known allergy or adverse reaction to anesthesia agents used in the procedure. * Previous tonsillar surgery or peritonsillar abscess drainage. * Severe comorbidities that may interfere with surgery or recovery (e.g., uncontrolled diabetes, heart failure). * Patients with craniofacial abnormalities affecting the airway. * Inability to understand or comply with study requirements.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Indus Hospital Karachi
Karachi, Sindh, 75500, Pakistan
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Other studies related to the condition(s) this trial covers.
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