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Levosimendan Administration and Outcome in Cardiac Surgery

Charité University Medicine Berlin logo

Charité University Medicine Berlin

Status

Completed

Conditions

Treatment of Left Heart Insufficiency in an Operative Setting of Cardiac Surgery

Treatments

Drug: Levosimendan

Study type

Observational

Funder types

Other

Identifiers

NCT02275013
ea1-044-13b

Details and patient eligibility

About

To assess the effects on outcome of levosimendan with respect to timing of its administration on the postoperative course of high-risk cardiac surgery patients in a retrospective observational study.

Enrollment

159 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • patients undergoing cardiac surgery between 2006 and 2013
  • levosimendan administration within 24 hours of postoperative ICU admission

Exclusion criteria

  • patients younger than 18

Trial design

159 participants in 2 patient groups

Early
Description:
Levosimendan administration within first hour of post-operative ICU admission
Treatment:
Drug: Levosimendan
Late
Description:
Levosimendan administration within 24 hours of post-operative ICU admission but after first hour
Treatment:
Drug: Levosimendan

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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