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Clinical Trial Summary

This study will assess the condition of orotracheal intubation in obese patients undergoing an elective bariatric surgery without the use of neuromuscular blocking agents. During the induction of general anesthesia, Propofol - Remifentanil combination will be used. The patients will be randomized in 2 groups with different doses of Remifentanil.

Clinical Trial Description

The prevalence of obesity increases steadily. For anesthesiologists, the airway management of obese patients is known to be difficult and at risk. Tracheal intubation needs to be successful quickly. Neuromuscular blocking agents allow this option but with a risk of anaphylaxis and respiratory complications. In fact, for many surgical procedures those drugs are not necessary. Numerous studies in non-obese patients with the combination of Remifentanil and Propofol have shown adequate conditions for tracheal intubation without neuromuscular blocking drugs. This combination has never been studied in obese patient. After randomization, induction of general anesthesia will be performed with 2,5 mg/kg of Propofol in association with either 3 µg/kg of Ideal Body Weight of Remifentanil, or 3 µg/kg + 30% of Ideal Body Weight of Remifentanil. Minutes after the induction, orotracheal intubation will be performed, and the Intubation Difficulty Scale recorded. Other data on hemodynamic, respiratory and airway management will be are collected during the surgery. In the Post Anaesthetic Care Unit (PACU),Any symptoms of traumatic airway management or aspiration are collected. Those data will be again looked for and collected on the day of the patient's discharge. ;

Study Design

Related Conditions & MeSH terms

NCT number NCT05026125
Study type Interventional
Source University Hospital, Toulouse
Contact Géraldine FAURE, MD
Phone 05 61 32 30 23
Email [email protected]
Status Not yet recruiting
Phase Phase 4
Start date October 2021
Completion date April 2023

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