OSA as a Remote Ischemic Preconditioning in Vascular Surgery

Sponsor
St. Anne's University Hospital Brno, Czech Republic (Other)
Overall Status
Recruiting
CT.gov ID
NCT04630535
Collaborator
Masaryk University (Other)
100
1
27
3.7

Study Details

Study Description

Brief 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.

Condition or Disease Intervention/Treatment Phase
  • Procedure: aorto-bifemoral bypass surgery

Detailed Description

Patients. Consecutive patients scheduled for elective aortobifemoral bypass (AAA and Leriche syndrome patients) will be recruited for this prospective, observational study.

Polygraphy (PG). PG measurements will be done two nights before surgery using the Embletta system (Embla - Embletta MPR PG Sleep Data Recording System).

STOP-BANG, Epworth questionnaire. Both questionnaires will be done the same day as polygraphy

Cardiovascular complications will be assessed from the first 30 post-operative days Pulmonary complications will be assessed from the first 30 post-operative days

Specific markers of I/R. T0 - before anesthesia induction T1 - 3 hrs after aorta de-clamping T2 - 12 hrs after aorta de-clamping T3 - 24 hrs after aorta de-clamping T4 - on the fifth post-operative day

Study Design

Study Type:
Observational
Anticipated Enrollment :
100 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
Obstructive Sleep Apnea as a Remote Ischemic Preconditioning in Patients Scheduled for Aorto-bifemoral Bypass Surgery
Actual Study Start Date :
Nov 1, 2020
Anticipated Primary Completion Date :
Dec 31, 2022
Anticipated Study Completion Date :
Jan 31, 2023

Arms and Interventions

Arm Intervention/Treatment
Obstructive Sleep Apnea

Pacient with OSA (AHI≥5) undergoing aorto-bifemoral bypass

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

Without Obstructive Sleep Apnea

Patinets without OSA undergoing aorto-bifemoral bypass

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

Outcome Measures

Primary Outcome Measures

  1. Change of I/R injury markers [T0 - before anesthesia induction; T1 - 3 hrs after aorta de-clamping; T2 - 12 hrs after aorta de-clamping; T3 - 24 hrs after aorta de-clamping; T4 - on the fifth post-operative day]

    Plasma Total Antioxidant Capacity and Reactive Oxygen Species Concentration

Secondary Outcome Measures

  1. post-operative complications [up to 30 post-operative days]

    cardiovascular and pulmonary post-operative complications

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts 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

Contacts and Locations

Locations

Site City State Country Postal Code
1 St. Anne's University Hospital Brno Brno Czech Republic Czechia 65691

Sponsors and Collaborators

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

Investigators

  • Principal Investigator: Ivan Cundrle, M.D., Ph.D., St. Anne's University Hospital in Brno

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Ivan Cundrle, Principal Investigator, St. Anne's University Hospital Brno, Czech Republic
ClinicalTrials.gov Identifier:
NCT04630535
Other Study ID Numbers:
  • IIT/2019/25
First Posted:
Nov 16, 2020
Last Update Posted:
May 4, 2022
Last Verified:
May 1, 2022
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Ivan Cundrle, Principal Investigator, St. Anne's University Hospital Brno, Czech Republic
Additional relevant MeSH terms:

Study Results

No Results Posted as of May 4, 2022