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RECRUITING
NCT05058612
PHASE4

Midodrine for the Early Liberation of Vasopressor Support in the ICU (LIBERATE Multi-Site)

Sponsor: University of Alberta

View on ClinicalTrials.gov

Summary

Vasopressors are medications that are given intravenously to increase the blood pressure of patients with illnesses that cause dangerous blood pressure drops. When a doctor prescribes a vasopressor, they ask that the dose be adjusted to achieve a specific blood pressure. This kind of medical support with intravenous (IV) vasopressors are usual treatments in intensive care unit (ICU) settings. Oral vasopressors, such as midodrine, have been historically used to maintain blood pressure in non-critically ill patients. In this study, the investigators will be using midodrine to reduce the need for IV vasopressors as blood pressure improves during the stay in the ICU. This LIBERATE multi-site study will continue the work of the LIBERATE feasibility RCT study to evaluate the role of midodrine for patients with low blood pressure in the ICU. It is comprised of the multi centre pilot RCT followed by the definitive multi centre RCT.

Official title: Midodrine for the Early Liberation From Vasopressor Support in the ICU - The LIBERATE Multi-Site Study

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

INTERVENTIONAL

Enrollment

870

Start Date

2021-03-22

Completion Date

2028-02

Last Updated

2026-01-20

Healthy Volunteers

Yes

Conditions

Interventions

DRUG

Midodrine

10 mg PO/NG q8h

DRUG

Placebo

Microcrystalline cellulose PO/NG 18h

Locations (1)

University of Alberta Hospital

Edmonton, Alberta, Canada