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Clinical Trials/NCT03624491
NCT03624491
Completed
Not Applicable

Mechanical Ventilation Guided By Transpulmonary and Airway Driving Pressures in the Setting of Intra-abdominal Hypertension

Mayo Clinic1 site in 1 country50 target enrollmentMarch 13, 2018
ConditionsSurgery

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Surgery
Sponsor
Mayo Clinic
Enrollment
50
Locations
1
Primary Endpoint
Airway driving pressure guided mechanical ventilation determined by esophageal balloon catheter measurements.
Status
Completed
Last Updated
4 years ago

Overview

Brief Summary

Esophageal pressure measurements in surgical patients requiring mechanical ventilation during abdominal laparoscopic or robotic surgeries requiring intra-abdominal insufflation.

Detailed Description

Decades of research and clinical observation in mechanical ventilation have demonstrated unequivocally that tidal volume (VT), plateau pressure (PPLAT) and PEEP (positive end-expiratory pressure) influence ventilator induced lung injury. Clinicians, however, have struggled in the attempt to find a single indicator of safety and risk. Recent analyses of the large multi-center randomized trials database suggest that Airway Driving Pressure (ADP) and Trans pulmonary Driving Pressure (DTP) are the variables of greatest importance and therefore the best single parameters on which to focus. In attempting to define their optimal values and their correlation between each other in the setting of intra-abdominal hypertension, we would like to compare standard of care mechanical ventilation (control) with mechanical ventilation guided by DTP and ADP (intervention) in patients undergoing abdominal laparoscopic surgery.

Registry
clinicaltrials.gov
Start Date
March 13, 2018
End Date
February 17, 2022
Last Updated
4 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Richard A. Oeckler, M.D., Ph.D.

Assistant Professor of Medicine and Physiology-Critical Care

Mayo Clinic

Eligibility Criteria

Inclusion Criteria

  • Patients requiring mechanical ventilation for abdominal laparoscopic and robotic surgeries.
  • Patients who are passively ventilated (no respiratory efforts) as a result of the sedation plan determined entirely by the primary anesthesia team --research team will not influence or participate on the sedation protocol plan or implementation.
  • Patients who are clinically stable and able to tolerate the changes in position that are routinely conducted as part of the standard of care in the operative room.
  • Patient/responsible family member signing the informed consent must speak English.
  • Exclusion criteria:
  • Patients with open abdomen prior to surgical procedures.
  • Females of childbearing age (18-50) with the potential to become pregnant and no clinically documented negative pregnancy test.
  • Patients with clinically evident spontaneous breathing efforts (ventilator wave forms) during surgical procedure.
  • Patients with clinical suspicion of elevated intra-cranial pressure (requiring head elevation).
  • Contraindication to body position change, as dictated by surgery-specific protocol.

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Airway driving pressure guided mechanical ventilation determined by esophageal balloon catheter measurements.

Time Frame: Through study completion, an average of one year

Optimizing the relationship between intra-abdominal pressure and both airway driving pressure and trans pulmonary driving pressure utilizing esophageal balloon measurements to guide mechanical ventilation.

Study Sites (1)

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