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Tonsillectomy clinical trials

View clinical trials related to Tonsillectomy.

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NCT ID: NCT01332253 Completed - Tonsillectomy Clinical Trials

Safety and Efficacy of Intravenous Ibuprofen for Treatment of Pain in Pediatric Patients Undergoing Tonsillectomy

Start date: July 2011
Phase: Phase 3
Study type: Interventional

That a single, pre-operative dose of intravenous ibuprofen will significantly reduce post-operative fentanyl use compared to placebo.

NCT ID: NCT01285804 Completed - Tonsillectomy Clinical Trials

Impact of Using a Cuffed Endotracheal Tube on Limiting the Risk of Airway Fire

Start date: January 2011
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate the impact of using a cuffed endotracheal tube (ETT) on the oxygen concentration in the oropharynx during adenoidectomy, tonsillectomy, or adenotonsillectomy. The study hypothesis is that inflation of the cuff on the ETT will eliminate contamination of the oropharynx with the inspired anesthetic gases and decrease the oxygen concentration in the oropharynx.

NCT ID: NCT01285687 Completed - Post-Operative Pain Clinical Trials

Acupuncture for Post-tonsillectomy Pain Control in Children

Start date: January 2011
Phase: N/A
Study type: Interventional

A randomized, controlled, single-blinded study comparing conventional postoperative analgesia with paracetamol-on-demand with the same regime plus acupuncture. The hypothesis is that postoperative treatment of children undergoing tonsillectomy with acupuncture will reduce pain with minimal unwanted effects.

NCT ID: NCT01228136 Completed - Tonsillectomy Clinical Trials

Tranexamic Acid and Pediatric Adenotonsillectomy

Start date: January 2010
Phase: Phase 4
Study type: Interventional

The purpose of this study is to determine if the use of tranexamic acid prior adenotonsillectomy in children can reduce surgical and postoperative bleeding.

NCT ID: NCT01141660 Completed - Tonsillectomy Clinical Trials

Use of Laryngeal Mask Airway in Pediatric Adenotonsillectomy

Start date: December 2007
Phase: N/A
Study type: Interventional

The aim of the current study is to compare the use of laryngeal mask airway (LMA) and endotracheal tube (ETT) in pediatric adenotonsillectomy. The primary objective is to assess the incidence of post-operative laryngospasm between the LMA and ETT. The investigators also sought to compare anesthetic, operative, and recovery times in the LMA and ETT groups. We hypothesized that the LMA would be a safe efficient alternative to the ETT.

NCT ID: NCT00849966 Completed - Pain, Postoperative Clinical Trials

Celecoxib for Pediatric Adenotonsillectomy

Start date: August 2009
Phase: Phase 2
Study type: Interventional

The investigators' study will involve the administration of either placebo or celecoxib to children aged 2 to 18 years of age undergoing tonsillectomy and assessing pain relief, impact on quality of life and side effect profile.

NCT ID: NCT00836264 Completed - Pharmacokinetics Clinical Trials

Pharmacogenomics Analysis of Morphine Pharmacokinetics in Pediatric Tonsillectomy and Adenoidectomy

Start date: January 2009
Phase:
Study type: Observational

Intravenous (IV) morphine requirement for immediate postoperative pain control depends upon the complex interplay of patient history, wound severity, environment, and genetics. Even for relatively uniform stimulus intensity, such as that associated with tonsillectomy and adenoidectomy (T&A), there can be marked individual variability in response to morphine. Some patients are refractory to standard doses and need increased amounts. Others are sensitive, require less drug to attain acceptable pain levels, and/or experience unwanted side effects that limit dosing. A significant number must be switched to different analgesics altogether. Despite the long clinical history of morphine as a postoperative analgesic, researchers have only begun to examine the origins of response variability. The investigators will look at 2000 retrospective Tonsillectomy and Adenoidectomy (T&A) cases and using this data and incorporating additional patient, surgical, and environmental factors that may contribute to response variability, the investigators then propose a prospective genome-wide association (GWA) study of 1500 children ages 4 to 18 years treated with IV morphine sulfate for day surgery T&A.

NCT ID: NCT00730340 Completed - Children Clinical Trials

Closure Method Study Following Tonsillectomy in Children

Start date: August 2008
Phase: Phase 0
Study type: Interventional

This is a children's study evaluating the effects of a tonsillectomy with tonsillar fossae closure compared to without closure of the operative wound.

NCT ID: NCT00662987 Completed - Tonsillectomy Clinical Trials

Effect of Duration of Antibiotic Therapy on Recovery Following Tonsillectomy

Start date: September 2005
Phase: N/A
Study type: Interventional

To determine whether a 3-day course of postoperative antibiotics is effective as a 7-day course in reducing pain and reducing time to resumption of normal diet and activity following pediatric tonsillectomy

NCT ID: NCT00581139 Completed - Pain, Postoperative Clinical Trials

Psychological Influences on Postoperative Recovery

NIH
Start date: April 2003
Phase: Phase 2
Study type: Interventional

The primary hypothesis tested in this project is that the preoperative behavioral stress response predicts postoperative behavioral and clinical recovery of children undergoing surgery.