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Endotracheal tube cuff pressure estimation techniques: safety and reliability among women undergoing general anaesthesia with intubation for cesarean sectio

Not Applicable
Conditions
Elective cesarean section
Pregnancy and Childbirth
Registration Number
ISRCTN66168037
Lead Sponsor
Habana Medical Services
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Ongoing
Sex
Female
Target Recruitment
389
Inclusion Criteria

1. Parturients scheduled for elective cesarean section under general anaesthesia with endotracheal intubation
2. Aged 18 to 40 years
3. American Society of Anesthesiologists Physical Status (ASA-PS) score 1-2

Exclusion Criteria

1. Patients with a history of difficult intubation or multiple attempts (more than three attempts) during intubation
2. Parturient requiring emergency intubation
3. Parturient with a higher risk for aspiration
4. Intubation performed by non-anaesthesia staff
5. Parturient with known anatomical laryngotracheal abnormalities
6. Those expected to remain intubated beyond the operation room period

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
<br> 1. Endotracheal tube cuff pressure determined using a standard manometer, predetermined volume of air (10 - 15 ml), or manual palpation of endotracheal tube pilot balloon immediately after intubation or prior to extubation. The technique used and the cuff pressure estimated in each group is recorded<br> 2. Cuff pressure associated complications (cough, sore throat, hoarseness, and blood-streaked expectoration) determined during an interview after 24 hours of extubation<br>
Secondary Outcome Measures
NameTimeMethod
Overall perioperative satisfaction, evaluated as 4 = excellent, 3 = good, 2 = satisfactory, 1 = poor, during an interview on the day of discharge
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