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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: NCT05639777 Recruiting - Clinical trials for Respiratory Tract Infections

Intranasal Dexmedetomidine in Children Undergoing Adenotonsillectomy Suffering From Mild Upper Respiratory Tract Infection

Start date: December 6, 2022
Phase: Phase 4
Study type: Interventional

The purpose of this study is to detect the efficacy of intranasal dexmedetomidine as a premedication to general anesthesia in pediatric patients with respiratory comorbidities undergoing adenotonsillectomy.

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: NCT05051189 Recruiting - OSA Clinical Trials

Effect of Opioids on Central Control of Ventilation in Children With Obstructive Sleep Apnea

Start date: December 1, 2021
Phase: Early Phase 1
Study type: Interventional

Children OSA exhibit varying responses to opioids. It is unknown if the degree of intermittent hypoxemia results in different opioid sensitivity

NCT ID: NCT04879823 Terminated - Surgery Clinical Trials

Post-operative Course of Dexamethasone to Reduce Tonsillectomy Morbidity

Start date: August 5, 2021
Phase: Phase 3
Study type: Interventional

The goal of this study is determine if an oral systemic course of steroids is a safe and effective option in lowering pain and complications following adenotonsillectomy in various pediatric age groups. A double blind, placebo-controlled randomized clinical trial of steroids (dexamethasone) versus placebo postoperatively will be performed. Investigators will determine if there is a difference in post-operative pain and complications between groups.

NCT ID: NCT04791761 Terminated - Opioid Use Clinical Trials

Non-Opioid Pain Medications After Intracapsular Adenotonsillectomy

Start date: April 13, 2021
Phase: Phase 1/Phase 2
Study type: Interventional

The goal of this study is to determine if non-opioid pain control is a safe way to manage pain after intracapsular adenotonsillectomy surgery in children. This study is the second part of our randomized clinical trials of assessing pain after adenotonsillectomy (T&A), the first being total T&A. The investigators will repeat the methodology in the first clinical trial by randomly assigning children aged 3-17 to one of two groups: one group will receive non-opioid pain medication only, and the other group will receive opioid and non-opioid medications for pain control. The investigators will analyze the data and determine if there is a difference in pain control between the two drug regimens, and if there are any other associated complications between the two groups. This study is important because if we can demonstrate that there is little difference in outcomes and pain control between the two groups, a strong argument can be made for reducing or eliminating opioid prescription after intracapsular adenotonsillectomy. This may protect future children from the risks of taking opioid medications and help to reduce the scope of the opioid epidemic.

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: NCT03618823 Terminated - Opioid Use Clinical Trials

Non-opioids for Analgesia After Adenotonsillectomy in Children

Start date: October 25, 2018
Phase: Phase 1/Phase 2
Study type: Interventional

The goal of this study is to determine if non-opioid pain control is a safe way to manage pain after adenotonsillectomy surgery in children. The investigators will be randomly assigning children aged 3-17 to one of two groups: one group will receive non-opioid pain medication only, and the other group will receive opioid and non-opioid medications for pain control. The investigators will analyze the data and determine if there is a difference in pain control between the two drug regimens, and if there are any other associated complications between the two groups. This study is important because if we can demonstrate that there is little difference in outcomes and pain control between the two groups, a strong argument can be made for reducing or eliminating opioid prescription after adenotonsillectomy. This may protect future children from the risks of taking opioid medications and help to reduce the scope of the opioid epidemic.

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.