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Comparison of Standard Versus Dynamic Compliance-Guided Individualized PEEP in Obese Patients Undergoing Spinal Surgery

A Prospective Interventional Study Comparing Standard and Dynamic Compliance-Guided Individualized Positive End-Expiratory Pressure on Intraoperative Oxygenation and Postoperative Pulmonary Complications in Obese Patients Undergoing Spinal Surgery

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07388719
Enrollment
80
Registered
2026-02-05
Start date
2025-02-02
Completion date
2025-12-12
Last updated
2026-02-05

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Obesity, Postoperative Pulmonary Complications, Mechanical Ventilation

Brief summary

This study aims to compare standard positive end-expiratory pressure (PEEP) with dynamic compliance-guided individualized PEEP in obese patients undergoing elective spinal surgery under general anesthesia. Obesity and prone positioning during spinal surgery are associated with reduced lung compliance, atelectasis, and an increased risk of postoperative pulmonary complications. Participants will be allocated to receive either a fixed standard PEEP or an individualized PEEP level determined according to intraoperative dynamic lung compliance. Intraoperative oxygenation, respiratory mechanics, arterial blood gas parameters, and hemodynamic variables will be assessed at predefined time points. Postoperative pulmonary complications within the first 24 hours after surgery will also be evaluated. The study seeks to determine whether individualized PEEP titration based on dynamic compliance offers physiological or clinical advantages compared with a standard PEEP strategy in this patient population.

Interventions

Application of a fixed positive end-expiratory pressure of 5 cmH₂O during intraoperative mechanical ventilation.

Sponsors

Konya City Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Intervention model description

Participants are assigned to one of two parallel groups receiving either standard fixed PEEP or dynamic compliance-guided individualized PEEP during surgery.

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* Adult patients aged 18-65 years * Body mass index (BMI) ≥30 kg/m² * Scheduled for elective spinal surgery under general anesthesia * Requirement for intraoperative mechanical ventilation * American Society of Anesthesiologists (ASA) physical status II-III * Provision of written informed consent

Exclusion criteria

* Pre-existing severe pulmonary disease (e.g., COPD GOLD stage III-IV, restrictive lung disease) * Severe cardiac disease (e.g., heart failure with reduced ejection fraction, significant valvular disease) * History of thoracic surgery affecting lung mechanics * Pregnancy * Emergency surgery * Intraoperative need for deviation from the planned ventilation protocol

Design outcomes

Primary

MeasureTime frameDescription
Intraoperative Oxygenation (PaO₂/FiO₂ Ratio)From induction of anesthesia until the end of surgeryThe primary outcome is intraoperative oxygenation assessed by the arterial partial pressure of oxygen to fraction of inspired oxygen (PaO₂/FiO₂) ratio during mechanical ventilation.

Secondary

MeasureTime frameDescription
Dynamic Lung ComplianceFrom induction of anesthesia until the end of surgeryDynamic lung compliance (mL/cmH₂O) measured intraoperatively via ventilator respiratory mechanics monitoring.
Static Lung ComplianceFrom induction of anesthesia until the end of surgeryStatic lung compliance (mL/cmH₂O) measured intraoperatively via ventilator plateau pressure analysis.
Peak Airway PressureFrom induction of anesthesia until the end of surgeryPeak inspiratory airway pressure (cmH₂O) measured intraoperatively using ventilator monitoring.
Plateau Airway PressureFrom induction of anesthesia until the end of surgeryPlateau airway pressure (cmH₂O) measured intraoperatively during mechanical ventilation.

Countries

Turkey (Türkiye)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 6, 2026