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RECRUITING
NCT05267886
PHASE4

CAPITAL DOREMI 2: Inotrope Versus Placebo Therapy for Cardiogenic Shock

Sponsor: Ottawa Heart Institute Research Corporation

View on ClinicalTrials.gov

Summary

The investigators are interested in determining if there is a meaningful benefit from the use of medications purported to increase the pumping function of the heart (i.e. inotropes) among critically ill patients admitted to the Cardiac Intensive Care Unit (CICU). To do this, the investigators will conduct a multi-centre, double blind, randomized control trial with patients who are deemed to require these medications by their treating physician to one of the two most commonly used agents in Canada (Milrinone or Dobutamine) or placebo. Each patient will be closely monitored by their healthcare team. The dose of medication will be adjusted according to each patients' clinical status. After 12 hours, the participants will move to open label treatment and any continued use of inotropes will be at the discretion of their treating physician.

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

INTERVENTIONAL

Enrollment

346

Start Date

2022-03-05

Completion Date

2026-12

Last Updated

2025-04-10

Healthy Volunteers

No

Interventions

DRUG

Dobutamine

Dobutamine administered according to its clinical dose stage for cardiogenic shock

DRUG

Milrinone

Milrinone administered according to its clinical dose stage for cardiogenic shock

DRUG

Normal Saline

Normal saline running at a standardized rate

Locations (3)

Mayo Clinic

Rochester, Minnesota, United States

Hamilton Health Sciences

Hamilton, Ontario, Canada

University of Ottawa Heart Institute

Ottawa, Ontario, Canada