Clinical Trial

Flow-Controlled Versus Volume-Controlled Ventilation in Lumbar Disc Herniation Surgery

Recruiting
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Summary
This prospective randomized trial aims to compare the effects of flow-controlled ventilation (FCV) and volume-controlled ventilation (VCV) on intraoperative airway pressures and oxygenation in patients undergoing lumbar disc herniation surgery under general anesthesia. Adult patients aged 18-65 years, with ASA physical status I-III and a body mass index of 18-30 kg/m², will be allocated to receive either FCV or VCV during routine intraoperative mechanical ventilation. Ventilatory parameters, including peak airway pressure, plateau pressure, pulmonary compliance, EtCO₂, SpO₂, and arterial blood gas variables, will be recorded at predefined time points after intubation. The primary endpoint is the PaO₂ value measured after 20 minutes in the prone position. By comparing respiratory mechanics and oxygenation between the two ventilation modes, this study aims to contribute to the optimization of intraoperative ventilatory management in lumbar disc herniation surgery.
Protocol Amendment History 1 change
critical Recruitment opened 2026-06-02
Trial Details
NCT Number NCT07614555
Lead Sponsor Ankara Etlik City Hospital
Conditions Lumbar Disc Herniation Surgery, Mechanical Ventilation
Enrollment 80 participants
Start Date 2026-05-28
Primary Completion 2026-11-12 (estimated)
Study Completion 2026-11-26 (estimated)
Updated on ClinicalTrials.gov 2026-06-01