CPAP in Patients With Severe Obesity After Anesthesia

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorMassachusetts General Hospital

About this trial

The goal of this study is to compare two continuous positive airway pressure (CPAP) settings on heart and lung function in patients with severe obesity after anesthesia. The main questions it aims to answer are:

1. Does a recruitment maneuver and CPAP set to intrathoracic pressure (ITP) improve cardiopulmonary function compared to standard CPAP settings in patients with severe obesity after anesthesia? 2. Does the location of adipose tissue influence the response to CPAP settings in patients with severe obesity after anesthesia?

Participants will undergo monitoring of their intrathoracic pressure using an esophageal catheter. In the recovery area after anesthesia, participants will receive two CPAP settings, each for 20 minutes.

* Intervention 1: Recruitment maneuver and CPAP will set to the level of intrathoracic pressure * Intervention 2: CPAP set to home settings (if OSA is present) or between 8-10 cmH20 (if OSA is not present).

Eligibility criteria

Qualifiers

Adult patients (≥ 18 years old) scheduled for elective non-cardiothoracic surgery requiring general anesthesia with an endotracheal tube

Planned admission to the post-anesthesia care unit (PACU) after surgery

BMI ≥ 40 kg/m2

Receiving ≤ 6 liters of supplemental nasal cannula oxygen

Disqualifiers

Pregnancy, suspected pregnancy or less than six weeks postpartum Known or current pneumothorax

systolic blood pressure <90 mmHg or >180 mmHg

mean blood pressure <60 or >130 mmHg

Any use of intravenous vasoactive agent

Trial design

Treatments tested in this trial

  • Recruitment/ITP-CPAP (Intervention A)
  • Standard CPAP (Intervention B)
  • Atmospheric Pressure

Treatment groups

60 Participants
are divided into 3 treatment groups

Locations

This trial has no locations

Sponsors and collaborators