NCT07277244
Low-Intensity Mechanical Ventilation in the Operating Room: a Pilot Study
Enrolling by Invitation
NAAges 18+InterventionalTreatmentBeth Israel Deaconess Medical CenterInvestigator-initiated
~60 participants
Updated 2026-06-02 on ClinicalTrials.gov
What's tested:Low Intensity Mechanical Ventilation
At a glance
Recruiting sites
0 of 1 listed site is recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
ΔEELV between baseline and after extubation before leaving the operating room.
Measured over Perioperative Day 0: From pre-intubation baseline in the operating room (prior to induction of anesthesia) to the first post-extubation EIT assessment (within 10 min after extubation on Day 0).
Conditions
Where it's being run
1 sites across 1 statesMassachusetts1
Who to contact
This trial hasn't published a contact. View it on ClinicalTrials.gov
Do you actually qualify for this trial?
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Eligibility criteria
Inclusion
Adult patients undergoing non-emergent intra-abdominal or pelvic robot-assisted surgery with an expected duration of at least 2 hours, under general anesthesia with planned extubation at the end of the procedure
Exclusion
Known pregnancy
Pre-existing intubation or tracheostomy
Contraindications for esophageal manometry: severe midface trauma or recent nasal surgery, esophageal varices, recent gastric or esophageal surgery
Contraindications for electrical impedance tomography (EIT): inability to place EIT belt, presence of an active electronic implantable device (e.g., pacemaker, ICD)
What this trial measures
- ΔEELV between baseline and after extubation before leaving the operating room.Perioperative Day 0: From pre-intubation baseline in the operating room (prior to induction of anesthesia) to the first post-extubation EIT assessment (within 10 min after extubation on Day 0).
Change in end-expiratory lung volume (EELV), measured using electrical impedance tomography between baseline and after extubation before leaving the operating room.