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NCT07774065Recruiting

Mechanical Ventilation in Obese Surgical Patients

Minimizing Post-Operative Pulmonary Complications in Patients With a BMI =35 kg/m2 Undergoing Robotic-Assisted or Conventional Laparoscopic Surgery

Source: ClinicalTrials.gov · Last updated 19 Aug 2026

Brief summary (registry, in English)

The purpose of this study is to evaluate whether an intraoperative positive end-expiratory pressures (PEEP) setting strategy aimed at minimizing the mechanical power delivered to the lungs via transpulmonary pressure improves postoperative outcomes in obese patients undergoing conventional laparoscopic or robotic-assisted surgery. The objectives are to determine whether this strategy reduces immediate postoperative hypoxemia, and to assess whether it mitigates lung injury as reflected by relevant blood biomarkers.

Status (registry)
Recruiting
Study type
Interventional
Enrollment
10 (estimated)
First submitted
11 Aug 2026
Start date
29 Jul 2026
Primary completion date
31 Jul 2027
Lead sponsor
The University of Texas Medical Branch, Galveston
Diseases
Obesity
NCT number
NCT07774065

What you commit to

  • Study type: Interventional
  • Planned participants: 10
  • From 29 Jul 2026 to the primary completion date, 31 Jul 2027
  • 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.

Prior treatment

  • Previous lung surgery;
  • Invasive mechanical ventilation for \>30 minutes within the last 30 days prior to surgery;
  • Receipt of immunosuppressive medication (chemotherapy or radiotherapy) up to two months prior to surgery;
  • Need for one-lung ventilation or planned re-intubation following surgery;

Other illness

  • Neurological procedures or cardiac surgery;
  • Severe chronic obstructive pulmonary disease (COPD, defined as non-invasive ventilation and/or oxygen therapy at home or repeated systemic corticosteroid therapy for acute exacerbations of COPD);
  • Severe cardiac disease (defined as New York Heart Association class III or IV, acute coronary syndrome or persistent ventricular tachyarrhythmia);
  • Acute respiratory distress syndrome (according to the Berlin definition 2) expected to require prolonged postoperative mechanical ventilation;
  • Severe pulmonary arterial hypertension (defined as systolic pulmonary artery pressure \> 40 mmHg)
  • Intracranial injury, intracranial tumor, or neuromuscular disease;
  • Known esophageal disease or anatomy that would preclude the safe placement of a standard orogastric tube

Lab values

  • Pregnancy, determined by anamnesis and/or laboratory testing;

Other

  • Requirement for intraoperative prone or lateral decubitus positioning;
  • Enrollment in another interventional study or refusal to give written informed consent;
  • Persistent hemodynamic instability or intractable shock, considered hemodynamically unsuitable for the study by the patient's managing physician;

Who the study is looking for

  • Age ≥ 18 years;
  • Body Mass Index (BMI) ≥ 35 kg/m2;
  • Scheduled for laparoscopic surgery expected to exceed 2h (from incision to closure) under general anesthesia, as determined pre-operatively by the attending surgeon and surgical team based on typical scheduling estimates, prior experience, procedure type, planned surgical approach, and patient-specific factors.

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
University of Texas Medical Branch - Galveston
Coordinator of this site? Confirm its status
GalvestonUnited StatesRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.