NCT Number: NCT00130871
Levosimendan Pretreatment for Weaning Patients From Cardio-Pulmonary Bypass
The study evaluates the efficacy of intravenous levosimendan treatment started during a coronary artery bypass operation to wean patients from a heart lung machine.
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Notify MeKey information
Conditions
Age range
18 year and older
Sex eligibility
All sexes
Study type
Interventional
Phase
Phase 2
Primary location
Helsinki University Central Hospital, Helsinki, Finland
About this study
Levosimendan or placebo infusion is started at the time of induction of anesthesia.
Who can participate
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
- Three vessel coronary artery disease.
- Indication for on-pump coronary artery bypass surgery.
- Ejection fraction below 50%
Exclusion criteria
- Indication for any cardiac valve surgery
- Previous coronary artery bypass surgery
Treatment and study plan
Primary outcomes
-
Proportion of successful primary weanings
Sponsors and collaborators
Lead sponsor
Orion Corporation, Orion Pharma
Industry
Registry information
Official study title
Impact of Levosimendan Pretreatment on Weaning From Cardiopulmonary Bypass (CPB) in Patients With Diminished Left Ventricular Function Before Coronary Artery Bypass Grafting (CABG)
Important dates
- Study start
- 2004
- Study completion
- 2006
- First posted
- Aug 16, 2005
- Registry last updated
- Feb 21, 2007
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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