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Physiologic Effects of CPAP After Vascular Surgery (PhyCUS)

U

University of Genova

Status

Unknown

Conditions

Postoperative Complications
Respiratory Failure

Treatments

Device: Postoperative preventive CPAP

Study type

Observational

Funder types

Other

Identifiers

NCT03543930
PhyCUS Study

Details and patient eligibility

About

This study aims to investigate, with a case-crossover design, the effects of a short course of preventive CPAP administered in the immediate postoperative period in patients at high-risk of developing postoperative pulmonary complications undergoing major vascular surgery.

Enrollment

18 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Open or endovascular surgery on the abdominal aorta
  • Surgical procedure requiring general anaesthesia and invasive intraoperative mechanical ventilation
  • Intermediate-high risk of postoperative pulmonary complications (ARISCAT score ≥ 26)

Exclusion criteria

  • Prolonged post-operative invasive ventilation
  • Invasive or non-invasive ventilation or oxygen therapy in the last month
  • ASA class IV or V
  • Emergency procedures
  • Pneumothorax or active pulmonary infection
  • Any contraindication to CPAP
  • Prolonged bed rest
  • Patient refusal to participate or to receive preventive CPAP

Trial design

18 participants in 2 patient groups

Major open vascular surgery
Description:
Surgical procedures on the abdominal aorta requiring median abdominal incision
Treatment:
Device: Postoperative preventive CPAP
Endovascular aortic repair
Description:
Abdominal aortic repair with endovascular approach
Treatment:
Device: Postoperative preventive CPAP

Trial contacts and locations

1

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Central trial contact

Paolo Pelosi, Prof.

Data sourced from clinicaltrials.gov

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