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Adenotonsillectomy clinical trials

View clinical trials related to Adenotonsillectomy.

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NCT ID: NCT06356298 Completed - Children Clinical Trials

Flexible Reinforced Laryngeal Mask Airway Versus Endotracheal Tube for Childhood Adenotonsillectomy

Start date: August 1, 2023
Phase: Phase 2
Study type: Interventional

The goal of this clinical trial is to compare the airway management effects of flexible reinforced laryngeal mask and endotracheal tube in childhood adenotonsillectomy. Participants will be randomly allocated to two groups: endotracheal tube group (ETT) and flexible reinforced laryngeal mask group (FLMA). For those in ETT group: they will be intubated after induction of anesthesia .For those in FLMA group: they will be put in flexible reinforced laryngeal mask after induction of anesthesia . The investigators will compare FLMA with ETT to see if flexible reinforced laryngeal mask can be used safely and effectively in childhood adenotonsillectomy,and if there will be less severe adverse events in FLMA.

NCT ID: NCT05364281 Completed - Tonsillectomy Clinical Trials

The Changes of ETT Cuff Pressures After Head and Neck Positions Placed for Adenotonsillectomy and Tonsillectomy in Children

Start date: August 1, 2019
Phase:
Study type: Observational

The main purpose of this study was to assess the effect of each of position (neck extension by under-shoulder pillow and Crowe-Davis retractor use) during adenoidectomy and adenotonsillectomy on the intracuff pressure of ETTs in children.

NCT ID: NCT04527393 Completed - Analgesia Clinical Trials

Individualized Analgesia for Pediatric Adenotonsillectomy

Start date: May 1, 2022
Phase: Phase 4
Study type: Interventional

The objective of this randomized clinical trial is to assess the safety and effectiveness of post-adenotonsillectomy analgesia with individualized opioid analgesia regime in children.

NCT ID: NCT03551067 Completed - Adenotonsillectomy Clinical Trials

Oral Dexmedetomidine for Parental Separation in Pediatrics Undergoing Adenotonsillectomy

Start date: August 1, 2016
Phase: Phase 4
Study type: Interventional

The efficacy of oral dexmedetomidine as sedative versus a combination of oral midazolam plus oral ketamine were compared regarding to satisfactory separation from parents, satisfactory mask induction and postoperative rescue analgesia in Pediatrics undergone Adenotosillectomy

NCT ID: NCT03378830 Completed - Sleep Apnea Clinical Trials

Pain at Home After Tonsillectomy With or Without Adenoidectomy

Start date: December 19, 2017
Phase:
Study type: Observational

The study type is a prospective observational cohort study of children undergoing adenotonsillectomy (T&A). The study will recruit the annual caseload of children undergoing T&A at the Montreal Children's Hospital, QC, Canada; aiming for 200 children. There are no interventions. The purpose of this study is to determine the severity and duration of postoperative pain after T&A and to link the severity of this pain with the severity of sleep disordered breathing.

NCT ID: NCT02501122 Completed - Adenotonsillectomy Clinical Trials

Retrospective Analysis in Quality of Care Measures in Pediatric Adenotonsillectomy Patients

Start date: December 2015
Phase: N/A
Study type: Observational

The purpose of this study is to interrogate the Partners for Kids (PFK) and the pediatric health information (PHIS) databases in addition to our own perioperative Nationwide Children's data base to look at outcomes, resource utilization, and cost trends for adenotonsillectomy in the nationally versus locally. The investigators also want compare Nationwide Children's to other regional and national tertiary pediatric institutions.

NCT ID: NCT02384187 Completed - Adenotonsillectomy Clinical Trials

Gabapentin Premedication and Adenotonsillectomy in Pediatric Patients

Start date: January 2015
Phase: Phase 3
Study type: Interventional

The frequent incidence of postoperative vomiting and severe pain in children undergoing adenotonsillectomy, may delay postoperative oral intake and increase the risk of dehydration. Postoperative nausea and vomiting (PONV) is of multi-factorial origin in this group of patients, with a reported incidence ranging from 23% to 73%. There is growing evidence that the perioperative administration of gabapentinin in adults is beneficial for preoperative anxiolysis, postoperative analgesia, reduction of postoperative nausea and vomiting, and delirium. Only few studies in literature explored the analgesic effects of preoperative gabapentin as premedication in pediatric population. However, the antiemetic effect of gabapentin in pediatric patients was not systematically investigated before.

NCT ID: NCT02228135 Completed - Tonsillectomy Clinical Trials

The Effect of Dexamethasone Dosing on Post-tonsillectomy Hemorrhage

Start date: September 2014
Phase: N/A
Study type: Observational

This is a retrospective chart review looking at the effect of dexamethasone dosing on post-tonsillectomy hemorrhage.

NCT ID: NCT01917097 Completed - Tonsillectomy Clinical Trials

Bradycardia Following Intraoperative Administration of Dexmedetomidine

Start date: August 2013
Phase: N/A
Study type: Observational

This is a retrospective chart review to evaluate the postoperative course of all pediatric patients admitted to the hospital following adenotonsillectomy over the past 24 months to evaluate the incidence of bradycardia in children who received dexmedetomidine intraoperatively and identify confounding factors which may be precipitating the bradycardia or potentiating the negative chronotropic effects of dexmedetomidine.

NCT ID: NCT01462539 Completed - Adenotonsillectomy Clinical Trials

Adenotonsillectomy and Obstructive Sleep Apnea Study

Start date: October 2011
Phase: N/A
Study type: Observational

Adenotonsillectomies are one of the most common childhood surgeries and are first-line treatment to correct childhood obstructive sleep apnea syndrome (OSAS). This is a study comparing patients with and without OSA looking at the length of stay following adenotonsillectomy and the factors affecting length of stay.