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6-month Follow up After Sevoflurane Postconditioning

University of Zurich (UZH) logo

University of Zurich (UZH)

Status

Completed

Conditions

Heart Surgical Procedures

Treatments

Other: no intervention; retrospective study

Study type

Observational

Funder types

Other

Identifiers

NCT02378168
KEK ZH 2014-0040

Details and patient eligibility

About

Retrospective analysis of a 6-month follow up within a randomised controlled study in cardiac surgery with pharmacological postconditioning (sedation on intensive care unit with sevoflurane)

Full description

Introduction: In a recent randomized controlled (RCT; NCT00924222) trial the investigators demonstrated in 102 patients that late post-conditioning with sevoflurane performed in the intensive care unit (ICU) reduced myocardial injury. These patients presented with lower troponin T values on the first post-operative day compared with patients undergoing propofol sedation. In order to assess possible clinical relevant long-term implications in patients enrolled in this study, the current retrospective analysis is performed focusing on cardiac and non-cardiac events during the first six months after surgery.

Methods: All patients who had successfully completed the late post-conditioning trial were included in this follow-up. Primary and secondary endpoints were the proportion of patients experiencing cardiac and non-cardiac events, respectively. Additionally, therapeutic interventions such as initiation or change of drug therapy, interventional treatment or surgery were assessed.

Enrollment

108 patients

Sex

All

Ages

18 to 90 years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

All patients who had successfully completed the late post-conditioning trial were included in this retrospective follow-up analysis. Written and informed consent of all patients included in the first study had to be available.

Trial design

108 participants in 1 patient group

cohort of RCT (StV 5-2007; NCT00924222)
Description:
Patient group with either sevoflurane or propofol sedation of the RCT (StV 5-2007; NCT00924222)
Treatment:
Other: no intervention; retrospective study

Trial contacts and locations

2

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Data sourced from clinicaltrials.gov

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