About this trial
This multicenter, prospective, randomized clinical trial aims to compare the effects of spinal (neuraxial) anesthesia with spontaneous ventilation versus general anesthesia with mechanical ventilation on the incidence of postoperative pulmonary complications in adult patients undergoing elective lower limb revascularization surgery. A total of 594 patients with symptomatic peripheral arterial disease will be randomly assigned to receive either spinal anesthesia with sedation or general anesthesia with mechanical ventilation. The primary outcome is the incidence of postoperative pulmonary complications within 30 days or until hospital discharge, including pneumonia, respiratory failure, pleural effusion, atelectasis, and other defined respiratory events. Secondary outcomes include cardiovascular events, hemodynamic instability, renal injury, delirium, extrapulmonary complications, adverse events in the operated limb, ICU and hospital length of stay, and mortality. The study will be conducted at Hospital de Clínicas de Porto Alegre, Hospital Nossa Senhora da Conceição, and other participating Brazilian centers, with an expected start date in July 2025 and completion in December 2029.
Eligibility criteria
Qualifiers
Adults aged ≥18 years
ASA physical status II to IV
Scheduled for elective peripheral arterial revascularization of the lower limbs
Diagnosis of symptomatic peripheral arterial disease with critical limb ischemia
Disqualifiers
Body mass index (BMI) > 40 kg/m²
Emergency vascular surgery
History of lung resection surgery
Persistent hemodynamic instability preoperatively
Trial design
Treatments tested in this trial
- Spinal Anesthesia
- General Anesthesia
Treatment groups
Sponsors and collaborators
Hospital de Clinicas de Porto Alegre
Lead sponsor
Grupo Hospitalar Conceição
Collaborator