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NCT07430111Recruiting

Flow-Controlled Versus Volume-Controlled Ventilation in Bariatric Surgery

Comparison of Flow-Controlled and Volume-Controlled Ventilation During Bariatric Surgery: A Prospective Randomized Trial

Source: ClinicalTrials.gov · Last updated 25 Feb 2026

Brief summary (registry, in English)

This prospective trial aims to compare the effects of flow-controlled ventilation (FCV) and volume-controlled ventilation (VCV) on intraoperative airway pressures and oxygenation in bariatric surgery under general anesthesia. Obesity is associated with altered respiratory mechanics, reduced functional residual capacity, and increased airway pressures, making the selection of an optimal ventilation strategy particularly important in this patient population. Adult patients aged 18-65 years with a body mass index ≥30 kg/m² and American Society of Anesthesiologists (ASA) physical status II-III will be allocated to receive either FCV or VCV as part of routine intraoperative mechanical ventilation. Ventilatory parameters, including peak and plateau airway pressures, pulmonary compliance, will be recorded at predefined intraoperative time points. The primary endpoint of the study is the PaO₂ value measured at the 20th minute under an FiO₂ of 0.8-1.0. By providing comparative data on respiratory mechanics and oxygenation, this study aims to contribute to the identification of lung-protective ventilation strategies and to optimize intraoperative ventilatory management in bariatric surgery.

Status (registry)
Recruiting
Study type
Interventional
Enrollment
40 (estimated)
First submitted
18 Feb 2026
Start date
24 Feb 2026
Primary completion date
5 Feb 2027
Lead sponsor
Ankara Etlik City Hospital
Diseases
Obesity
NCT number
NCT07430111

What you commit to

  • Study type: Interventional
  • Planned participants: 40
  • From 24 Feb 2026 to the primary completion date, 5 Feb 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

  • Known or previously diagnosed pulmonary disease
  • Patients with markedly altered lung anatomy or function due to prior major thoracic surgery
  • Patients who were dependent on supplemental oxygen therapy in the preoperative period

Other illness

  • Patients with severe preoperative pulmonary function impairment (e.g., FEV₁ \< 50% predicted, severe restrictive or obstructive pathology)

Other

  • ASA physical status I or IV and above
  • Refusal to participate in the study or inability to comply with study procedures

Who the study is looking for

  • Age between 18 and 65 years
  • Body mass index (BMI) ≥ 30 kg/m²
  • ASA physical status II-III

Age in the registry: 18 years to 65 years · 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
Ankara Etlik City Hospital
Coordinator of this site? Confirm its status
AnkaraTurkey (Türkiye)Recruiting

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