Exploring the effects of obstructive sleep apnea on vascular surgery outcomes

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This observational study aims to investigate the relationship between obstructive sleep apnea (OSA) and ischemia-reperfusion (I/R) injury in patients undergoing elective aortobifemoral bypass surgery for abdominal aortic aneurysm repair. Patients will be assessed for OSA severity using polygraphy and questionnaires prior to surgery. The study will monitor postoperative complications and specific markers of I/R at various time points following surgery to determine if OSA has a protective effect against I/R injury. The findings could provide insights into optimizing surgical outcomes for patients with OSA.

Why it matters

Who can join: the full rules

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

Where it's running

• St. Anne's University Hospital Brno
  Brno, Czech Republic, Czechia Recruiting

Study contacts

• Principal investigator: Ivan Cundrle, M.D., Ph.D. — St. Anne's University Hospital in Brno
• Study coordinator: Ivan Cundrle, M.D., Ph.D.
• Email: ivan.cundrle@fnusa.cz
• Phone: 00420543182553

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.