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Clinical Trials in Czechia / NCT04630535
Recruiting Observational

OSA as a Remote Ischemic Preconditioning in Vascular Surgery

NCT04630535 · tracked via the Priya Life Science Czechia tracker
Phase
Observational
Started
2020-11-01
Last updated
2026-04-27

Condition(s) studied

Obstructive Sleep ApneaVascular AneurysmIschemia Reperfusion Injury

Investigational drug(s) / intervention(s)

aorto-bifemoral bypass surgery

aorto-bifemoral bypass surgery: aorto-bifemoral bypass surgery (Leriche syndrom, elective AAA repair)

Study summary

Ischemia and reperfusion (I/R) injury during abdominal aortic aneurysm (AAA) repair is inevitable and may lead to postoperative multi-organ failure. Remote ischemic preconditioning (short periods of ischemia in anticipation of longer period of ischemia) may act protectively against ischemia.

Studies of ischemic preconditioning in patients with AAA are conflicting. Obstructive sleep apnea (OSA) is a sleep disordered breathing syndrome which may have a protective effect against ischemia.

The investigators hypothesize that I/R injury will be less pronounced in patients who have OSA and that the extent of I/R injury will inversely correlate with OSA severity. Accordingly, the aim of this study is to compare postoperative complications and markers of I/R in patients undergoing elective AAA repair who do and do not have OSA.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * patients scheduled for elective aorto-bifemoral bypass (AAA and Leriche syndrome patients) Exclusion Criteria: * emergent surgery * aorto-bifemoral bypass using deep vein graft * re-operations * known OSA with CPAP treatment

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
St. Anne's University Hospital Brno Brno Czech Republic Recruiting

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT04630535 on ClinicalTrials.gov ↗ ← All trials in Czechia