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

Phase 4
Recruiting
Conditions
Vasoplegia
Interventions
Drug: Placebo
Registration Number
NCT05058612
Lead Sponsor
University of Alberta
Brief 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.

The LIBERATE multi-site study will continue the work of the pilot study to evaluate the role of midodrine for patients with low blood pressure in the ICU.

Detailed Description

Purpose: Resuscitation and hemodynamic support with intravenous (IV) vasopressors is a prime indication of treatment in intensive care unit (ICU) settings. Hemodynamic support is typically provided with intravenous (IV) vasopressors. However, these have been shown to have significant negative effects including increased central venous catheter line associated infections, venous thromboembolic disease, impaired mobility and gastrointestinal injury and ischemia. Oral vasopressors, such as midodrine, have been historically used for hemodynamic support in non-critically ill patients, but their study in patients as IV pressor sparing therapy has been limited.

Hypothesis: to evaluate the expanded role of midodrine for any vasoplegic patients in the ICU.

Justification: In 2018, there were 1,613 admissions to the adult general systems ICU (GSICU) at the University of Alberta Hospital (UAH). Patients were sick, with a mean Acute Physiology and Chronic Health Evaluation II (APACHE) score of 21.3, with 36.4% requiring vasopressors on admission, accounting for 1942 patient-days (data from eCritical TRACER database). In the environment strained healthcare resources and limited ICU capacity, the ability to safely wean patients from IV vasopressors with transition to oral hemodynamic supporting agents would greatly improve how patients navigate through the healthcare system. This in turn will improve patient-centered case.

Primary Objective:

To compare the effect of enteral midodrine vs. placebo in critically ill patients with vasoplegia receiving continuous IV vasopressor therapy on ICU length of stay.

Secondary Objectives: To compare the effect of enteral midodrine vs. placebo on: Total and post-hospital length of stay, Duration of IV vasopressor support, 90-day all-cause mortality, Rates of ICU re-admission, Rate of re-initiation of IV vasopressors.

Tertiary Objectives: To determine the health economic effects of the usage of midodrine vs placebo on: ICU costs, Hospital costs, Total healthcare costs, Cost-effectiveness.

Safety Endpoints: Adverse drug reactions, Serious adverse drug reactions, Suspected unexpected serious adverse reactions.

Research Method/Procedures: The LIBERATE Trial is a multi center, concealed-allocation parallel-group blinded randomized controlled trial. Patients will be randomly assigned to midodrine (enteral, 10mg every 8h) or placebo (microcrystalline cellulose) for the duration of their IV vasopressor therapy and 24h following the discontinuation of their IV vasopressor therapy. The recruitment target for the multi centre pilot RCT is 350 subjects (i.e., 175 subjects per arm), followed by the definitive RCT with a recruitment target of 850 subjects (425 subjects per arm). A blinded multi site pilot analysis will be conducted after the enrolment of the first 20% of study subjects (170 subjects).

Recruitment & Eligibility

Status
RECRUITING
Sex
All
Target Recruitment
350
Inclusion Criteria
  • Age > 18 years
  • Ongoing vasopressor support
  • Decreasing vasopressor dose(s)
Exclusion Criteria
  • Greater than 24 hours from peak vasopressor dose
  • Contraindication to enteral medications
  • Previously received midodrine in last 7 days
  • Expected death or anticipated withdrawal of life-sustaining therapies in next 24 hours
  • Pregnancy
  • Known allergy to midodrine

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
PlaceboPlaceboMicrocrystalline cellulose PO/NG q8h
MidodrineMidodrineMidodrine 10 mg PO/NG q8h
Primary Outcome Measures
NameTimeMethod
Hierarchical composite of 30-day mortality and ICU length of stay1 year

The effects of midodrine on patient mortality at 30 days or total duration of patient stay in ICU

Secondary Outcome Measures
NameTimeMethod
Total and post-ICU length of stay1 year

The total duration of patient stay in hospital and the duration of hospital stay after ICU discharge

Duration of vasopressor support1 year

Duration of intravenous vasopressor support

ICU readmission1 year

Rate of ICU re-admissions during the index hospitalization

Re-initiation of vasopressors1 year

Rate of re-initiation of intravenous vasopressors during ICU stay

Mortality1 year

All cause mortality within 90 days of study recruitment

ICU costs1 year

Total cost of ICU stay

Hospital costs1 year

Total cost of hospital stay

Total health care costs1 year

Total healthcare costs

Cost effectiveness1 year

Incremental costs and effectiveness based on daily ICU costs

Trial Locations

Locations (1)

University of Alberta Hospital

🇨🇦

Edmonton, Alberta, Canada

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