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Tonsillar Hypertrophy clinical trials

View clinical trials related to Tonsillar Hypertrophy.

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NCT ID: NCT06187194 Recruiting - Clinical trials for Tonsillar Hypertrophy

Efficacy and Safety of an Irreversible Electroporation (IRE) System for Tonsil Reduction for The Treatment of Chronic Symptomatic Tonsillar Hypertrophy

Start date: December 5, 2023
Phase: N/A
Study type: Interventional

The purpose of the IRE System is to address the clinical need for reducing the volume of chronic symptomatic hypertrophic tonsil(s) while minimizing side effects and complications. Procedure time will also be reduced. The IRE System is designed to be more comfortable for patients, as it employs a noninvasive procedure using a high voltage pulsed electric field to create irreversible nanopores in the cell membrane, leading to cell death and the reduction of tonsil volume.

NCT ID: NCT05575401 Recruiting - Clinical trials for Sleep Apnea, Obstructive

Lateral Pharyngoplasty Outcomes in Children Undergoing Tonsillectomy

Start date: May 17, 2023
Phase: N/A
Study type: Interventional

The goal of this treatment study is to determine if doing lateral pharyngoplasty with tonsillectomy is better for children than doing tonsillectomy alone. The main questions it aims to answer are: - Do children experience less pain after surgery when lateral pharyngoplasty is performed with tonsillectomy compared to tonsillectomy alone? - Do children eat/drink better when lateral pharyngoplasty is performed with tonsillectomy compared to tonsillectomy alone? - Is there a lower risk of bleeding after tonsillectomy when lateral pharyngoplasty is performed? Researchers will compare children undergoing tonsillectomy and lateral pharyngoplasty with children undergoing tonsillectomy alone to see if the participants experience less pain, better oral intake, and less bleeding complications after surgery. Parents of participants will be asked to record pain scores and pain medications given, approximate amounts of daily oral intake, and any complications after surgery.

NCT ID: NCT04314492 Recruiting - Clinical trials for Sleep Apnea, Obstructive

Intracapsular Tonsillectomy in the Treatment of Obstructive Sleep Apnea in Adults

Start date: September 1, 2020
Phase: N/A
Study type: Interventional

Treating sleep apnea in adults caused by tonsillar hypertrophy with intracapsular tonsillectomy by coblation

NCT ID: NCT02818647 Recruiting - Tonsillectomy Clinical Trials

Comparison of Cold Dissection Technique and Needle Monopolar Electrocautery Tonsillectomy

TONSIL
Start date: June 2016
Phase: N/A
Study type: Interventional

Patients 13-years-or older who undergo tonsillectomy operation (without another additional surgery) will be enrolled in the study. Randomly, one side is going to be operated with conventional cold-knife technique and hemostasis will be maintained with bipolar diathermy (25-30w). Contralateral tonsil is going to be operated with needle-tip monopolar electrocautery (10-12w) at Blend 1 mode and hemostasis will also be maintained with needle-tip monopolar cautery. Postoperative tonsillar fossa healing and pain is going to be evaluated for both sides separately with Visual Analogue Scale. All operations are going to be performed by a single surgeon and all evaluations are going to be carried out by another surgeon in a totally blinded fashion to avoid possible bias.