Clinical Trials Directory

Trials / Completed

CompletedNCT05021549

Apneic Oxygenation for Morbid Obese Parturient in cs

Effectiveness of Apneic Oxygenation for Morbid Obese Parturient Performing Elective Caesarean Section Under General Anesthesia

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
60 (actual)
Sponsor
Ain Shams University · Academic / Other
Sex
Female
Age
18 Years
Healthy volunteers
Accepted

Summary

The aim of this study is to compare the effect of apneic preoxygenation to conventional preoxygenation on the oxygen desaturation in morbid obese parturient performing elective caesarean section under general anesthesia.

Detailed description

Anesthetic management of the obese parturient is challenging. Both pregnancy and obesity are risk factors for a difficult airway and anesthesia-related maternal mortality. There is increased risk of difficult intubation associated with an increased difficultly in mask ventilation and increased risk of accelerated desaturation during apnea. The use of apneic oxygenation for the optimization of peri-intubation conditions is a promising means of preventing hypoxemia. Despite the recommendation of the use of nasal prongs to insufflate oxygen at flows of 5 L/min to 15 L/min during the apneic period randomized controlled trial is still not available in the morbidly obese parturient.

Conditions

Interventions

TypeNameDescription
DEVICEnasal prongapneic preoxygenation group (30 patients), will receive 10 L/ min of O2 via nasal prong during preintubation apnia

Timeline

Start date
2021-09-15
Primary completion
2022-04-01
Completion
2022-04-10
First posted
2021-08-25
Last updated
2022-06-07

Locations

2 sites across 1 country: Egypt

Source: ClinicalTrials.gov record NCT05021549. Inclusion in this directory is not an endorsement.