NCT07531602Enrolling by invitation
Effect of PEEP on Cardiac Function
The Effect of Positive End-Expiratory Pressure on Biventricular Mechanics in the Perioperative Setting
Source: ClinicalTrials.gov · Last updated 1 Jul 2026
Brief summary (registry, in English)
The purpose of this single-center, prospective study is to evaluate the physiologic effect of changes in PEEP on biventricular mechanics and RV-pulmonary arterial (RV-PA) coupling in adult patients undergoing cardiac surgery.
- Status (registry)
- Enrolling by invitation
- Study type
- Interventional
- Enrollment
- 28 (estimated)
- First submitted
- 9 Apr 2026
- Start date
- 17 Jun 2026
- Primary completion date
- 30 Jul 2028
- Lead sponsor
- Beth Israel Deaconess Medical Center
- Diseases
- Coronary artery disease
- NCT number
- NCT07531602
What you commit to
- Study type: Interventional
- Planned participants: 28
- From 17 Jun 2026 to the primary completion date, 30 Jul 2028
- 1 site in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Other illness
- 1\. Significant arrhythmia (e.g., atrial fibrillation with uncontrolled ventricular response or other rhythm disturbances) that would interfere with reliable pressure waveform or echocardiographic measurements.
- 2\. Severe valvular disease where protocol-related PEEP changes may pose unacceptable hemodynamic risk, as determined by the clinical team.
- 3\. Significant chronic lung disease or other pulmonary pathology where PEEP adjustments may be unsafe (e.g., severe COPD with dynamic hyperinflation, bullous lung disease), at the discretion of the anesthesia team.
Other
- 4\. Contraindication to changes in PEEP, including inability to tolerate the planned PEEP titration due to hemodynamic instability or clinician concern.
- 5\. Any contraindication to TEE (if clinically required TEE is not performed or is contraindicated, the subject will not be eligible)
- 6\. Investigator or clinical team discretion (e.g., safety concerns, inability to obtain reliable measurements, or conflict with other perioperative research protocols)
Who the study is looking for
- 1\. Age ≥ 18 years
- 2\. Scheduled to undergo cardiac surgery requiring general anesthesia
- 3\. Planned use of intraoperative transesophageal echocardiography (TEE) as part of routine clinical care
- 4\. Planned placement of a pulmonary artery catheter as part of clinical care (Pulmonary artery catheter placement will be performed solely based on clinical judgment by the treating anesthesia and surgical teams. At our institution, pulmonary artery catheters are routinely placed in cardiac surgery patients with clinical indications including:
- preoperative pulmonary hypertension (e.g., estimated PCWP \>20 mmHg or elevated filling pressures on preoperative echocardiography),
- right ventricular dysfunction or suspected RV failure (preoperative visual TTE assessment),
- significant cardiopulmonary comorbidity,
- or anticipated complex, prolonged, or high-acuity cardiac surgery. The research team will not influence decisions regarding catheter placement. Only patients already scheduled to receive a clinically indicated pulmonary artery catheter will be eligible for enrollment.)
- 5\. Able and willing to provide written informed consent prior to surgery
Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers
Sites (1)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Beth Israel Deaconess Medical Center Coordinator of this site? Confirm its status | Boston | United States | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.