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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00959569
Other study ID # GO/URC/ER/mm 459/DG
Secondary ID
Status Completed
Phase Phase 4
First received
Last updated
Start date August 2009
Est. completion date June 2018

Study information

Verified date October 2018
Source Università Vita-Salute San Raffaele
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This large randomized double-blind clinical trial (esmolol vs placebo) will enroll patients undergoing cardiac surgery to study the additive cardiac protection of this therapeutic strategy.


Recruitment information / eligibility

Status Completed
Enrollment 200
Est. completion date June 2018
Est. primary completion date May 2018
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- end diastolic diameter >60 mm and/or an ejection fraction <50%

- written informed consent

- age >18 years

Exclusion Criteria:

- previous unusual response to esmolol

- inclusion in other randomized studies

- esmolol administration in the previous 30 days

- emergency operation

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Esmolol
esmolol (1-3 mg/kg) during cardiac surgery
Placebo
normosaline (same ml of the study drug)

Locations

Country Name City State
Italy Vita-Salute University Milano

Sponsors (1)

Lead Sponsor Collaborator
Università Vita-Salute San Raffaele

Country where clinical trial is conducted

Italy, 

References & Publications (4)

Crescenzi G, Landoni G, Zangrillo A, Guarracino F, Rosica C, La Canna G, Alfieri O. Management and decision-making strategy for systolic anterior motion after mitral valve repair. J Thorac Cardiovasc Surg. 2009 Feb;137(2):320-5. doi: 10.1016/j.jtcvs.2008.08.018. — View Citation

Crescenzi G, Rosica C, Marino G, Serini SM, Covello RD, Landoni G, Zangrillo A. The use of esmolol to treat systolic anterior motion of the mitral valve after mitral valve repair. Eur J Anaesthesiol. 2008 Apr;25(4):342-3. doi: 10.1017/S0265021507002876. — View Citation

Landoni G, Zambon M, Zangrillo A. Reducing perioperative myocardial infarction with anesthetic drugs and techniques. Curr Drug Targets. 2009 Sep;10(9):858-62. Epub 2009 Sep 1. Review. — View Citation

Zangrillo A, Turi S, Crescenzi G, Oriani A, Distaso F, Monaco F, Bignami E, Landoni G. Esmolol reduces perioperative ischemia in cardiac surgery: a meta-analysis of randomized controlled studies. J Cardiothorac Vasc Anesth. 2009 Oct;23(5):625-32. doi: 10.1053/j.jvca.2009.01.003. Epub 2009 Mar 18. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Composite endpoint of number of dead patients and/or number of patients requiring prolonged ICU stay. Hospital stay (approximately 2 weeks)
Secondary Number of patients with ventricular fibrillation after cardiopulmonary bypass 30 days and 1 year
Secondary Number of patients with low cardiac output syndrome 30 days and 1 year
Secondary Number of patients requiring post-operative inotropic support 30 days and 1 year
Secondary peak postoperative cardiac troponin level 30 days and 1 year
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