New treatment option for Postoperative Period
Official title Positive Pressure Therapy to Optimize LUNG Function After Heart Surgery
ClinicalTrials.gov ID: NCT06611527
What this study is testing
- What it's testing
- The most common cardiac surgeries are myocardial revascularization and valve replacement or plastic surgery. In the postoperative period of cardiac surgeries, the incidence of pulmonary complications ranges from 30% to 50% and is associated with increased length of hospital stay and morbidity and mortality.
- Which group you join is decided by chance.
A plain-language read of the study's public ClinicalTrials.gov listing. The study team confirms the details.
Who can take part
Ages 18 and older
You may be able to join if
- Immediate postoperative period of myocardial revascularization and/or valve replacement or plastic surgery;
- Patients in the preoperative period at risk of developing pulmonary complications, characterized by the presence of at least 2 of the following risk...
You likely can't join if
- Hemodynamic instability characterized by mean arterial pressure (MAP) lower than 60mmHg and/or acute arrhythmia of any etiology;
- Need for intra-aortic balloon;
- Duration of invasive mechanical ventilation exceeding 24 hours after surgery;
- Pulmonary complication score ≥ grade 3;
- Presence of signs of acute respiratory failure, such as respiratory rate (f) ≥ 25 breaths/min and use of accessory muscles;
- Chest tube with air leak;
See the full eligibility criteria
- Immediate postoperative period of myocardial revascularization and/or valve replacement or plastic surgery;
- Patients in the preoperative period at risk of developing pulmonary complications, characterized by the presence of at least 2 of the following risk factors: age ≥ 70 years, productive cough, diabetes, history of...
- Hemodynamic instability characterized by mean arterial pressure (MAP) lower than 60mmHg and/or acute arrhythmia of any etiology;
- Need for intra-aortic balloon;
- Duration of invasive mechanical ventilation exceeding 24 hours after surgery;
- Pulmonary complication score ≥ grade 3;
- Presence of signs of acute respiratory failure, such as respiratory rate (f) ≥ 25 breaths/min and use of accessory muscles;
- Chest tube with air leak;
- Use of a pacemaker or implantable or external cardioverter-defibrillator.
The study team makes the final eligibility decision.
Where it's taking place
- São Paulo, São Paulo, Brazil
Questions & answers
Do participants get paid in this trial?
This listing doesn't specify compensation. Many trials still reimburse travel or offer a stipend, so it's worth asking the study team when you connect.
Is it free to join, and do I need insurance?
Searching and applying through BridgeMD is free. In clinical trials the study-related treatment and visits are generally provided at no cost to you. You usually don't need insurance to take part - confirm specifics with the study team.
How long does this study last?
The listing doesn't state an exact length. The study team walks you through the schedule and number of visits before you decide to enroll.
Who can join this trial?
This study is enrolling all sexes, 18 years and older. The study team makes the final eligibility decision.
Where is this trial taking place?
Study sites include São Paulo, São Paulo, Brazil. Enter your location above to see the nearest site and check your eligibility.
Explore other conditions
BridgeMD is an information and trial-matching tool - not medical advice, and not the study sponsor. Details come from ClinicalTrials.gov; the study team decides eligibility.