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Safety Profile of the Combination of Levosimendan and IV Beta Blocker in Cardiogenic Shock: a Retrospective Study (SeLeBêta)

C

Central Hospital, Nancy, France

Status

Unknown

Conditions

Arrythmia
Cardiogenic Shock

Study type

Observational

Funder types

Other

Identifiers

NCT04938375
2021PI069

Details and patient eligibility

About

The purpose of this study is to assess the safety profile of the combination of Levosimendan and beta blocker in cardiogenic shock with arrythmia.

Enrollment

25 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Adult patients admitted to the ICU for cardiogenic shock who received esmolol or landiolol within 7 days of a levosimendan treatment

Exclusion criteria

  • Patient's opposition

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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