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Tonsillectomy clinical trials

View clinical trials related to Tonsillectomy.

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NCT ID: NCT01904461 Recruiting - Clinical trials for Postoperative Complications

HemORL: Monocentric, Prospective, Comparative Study on the Use of a Haemostatic Vacuum Device During Tonsillectomy in Children

HemORL
Start date: October 2014
Phase: N/A
Study type: Interventional

The long-term objective of this study is to prove: - the equivalence of the number of post-operation hemorrhages, and maybe a decrease of the number of secondary hemorrhages - the decrease of pain and quicker re-feeding - an easier haemostasis - the simplification of the tonsillectomy surgical kit - the decrease of dissection time

NCT ID: NCT01605903 Completed - Tonsillectomy Clinical Trials

Postoperative Ibuprofen and the Risk of Bleeding After Tonsillectomy With or Without Adenoidectomy

Start date: May 3, 2012
Phase: Phase 2
Study type: Interventional

Tonsillectomy (the surgical removal of the tonsils) is a commonly performed surgery in children. One risk of tonsillectomy is postoperative bleeding, and this can be more dangerous in children because their blood volume is lower than adults. Ibuprofen, a nonsteroidal anti-inflammatory medication (NSAID), is an effective pain medication. Recent guidelines, published by the American Academy of Otolaryngology, advocated use of ibuprofen after tonsillectomy. However, NSAIDs are associated with altered platelet function and a theoretical increased risk of bleeding after surgery. The investigators would like to explore the effect that ibuprofen has on postoperative bleeding, as well as validate previous studies demonstrating it is an effective pain medication after tonsillectomy.

NCT ID: NCT01582022 Not yet recruiting - Tonsillectomy Clinical Trials

Evaluation of The Effect of Bupivacaine (Marcaine) in Reducing Early Post Tonsillectomy Pain

Start date: n/a
Phase: Phase 4
Study type: Interventional

Research Methodology: It will be a prospective, randomized, placebo-controlled, single-blind, intra-individual study in which one tonsillar fossa will be the tested side, and the other fossa will be the control. And the tested side will be packed with bupivacaine for five minutes. In the other hand, the controlled side will be packed for five minutes with gauze soaked in normal saline. The selection of the tested side and controlled side will be randomized based on the last digit in the medical record number (i.e. if the last digit is even then the tested side is the right and if the last digit is odd then the tested side is the left). Pain evaluation will be by visual analog scale and it will be in frequency of 2, 4, 6, 8, 12, 24 hours post-op.

NCT ID: NCT01552096 Completed - Postoperative Pain Clinical Trials

Tramadol Versus Lidocaine Infiltration for Tonsillectomy

Start date: December 2011
Phase: Phase 2
Study type: Interventional

The investigators postulate that the use of pre-incisional peritonsillar infiltration of tramadol or lidocaine reduces both the inflammatory response and postoperative analgesic consumption, without harmful effects. Therefore, the present study is designed to evaluate the effects of infiltration of tramadol or lidocaine on the postoperative acute-phase serum protein, C-reactive protein, and analgesic consumption after tonsillectomy.

NCT ID: NCT01528891 Completed - Tonsillectomy Clinical Trials

Dexmedetomidine as a Rapid Bolus in Children for Emergence Agitation

Start date: January 2012
Phase: Phase 3
Study type: Interventional

To Determine The Efficacy of a Rapid Bolus Injection of Dexmedetomidine on the Incidence of Emergence Agitation in Anesthetized Children and the Cardiovascular Profile of a Rapid Bolus Injection of Dexmedetomidine.

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: NCT01275079 Recruiting - Tonsillectomy Clinical Trials

Change of Nasalance After Tonsillectomy in Thai Adult

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

The purpose of this study is to analyze the change of nasalance after tonsillectomy in Thai adults.

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.