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CEPEC Platform - Comparision of MAP targets in shock and their outcomes

Canadian Critical Care Comparative Effectiveness Platform(e) devaluation clinique comparee en soins critiques - Vasopressor Domain - CEPEC- Vasopressor Domain

Status
Active, not recruiting
Phases
Phase 2Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/03/106489
Enrollment
10000
Registered
2026-03-18
Start date
Unknown
Completion date
Unknown
Last updated
2026-03-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: I00-I99- Diseases of the circulatory system

Interventions

Intervention1: MAP targets at differnt ranges. 55-60: Randomised to a MAP range, and the outcomes are compared against each other Intervention2: MAP targets at differnt ranges. 60-65: Randomised to a

Sponsors

Sunnybrook Health Sciences Centre
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1 Ongoing vasopressor infusion to treat hypotension, or would be used to treat clinician defined hypotension as part of usual care; 2 MAP less than 75 mmHg at any point or lower than the upper value of the highest mean arterial pressure target range activated locally 3 Patient expected to be in the ICU for more than 48 hours.

Exclusion criteria

Exclusion criteria: 1. Treating team does not have equipoise for at least two consecutive MAP target ranges in the CEPEC Vasopressor Domain; 2. Acute traumatic brain injury (within 7 days or ongoing active treatment for elevated intracranial pressure); 3. Acute subarachnoid haemorrhage (within 21 days); 4. Acute spinal cord injury (within 7 days of injury or ongoing vasopressor therapy for suspected spinal cord ischemia); 5. Lung, heart, liver, kidney transplant recipient (within 7 days); 6. More than 24 hours since meeting the inclusion criteria in the ICU; 7. Previously randomised into the CEPEC Vasopressor Domain or a confounding trial

Design outcomes

Primary

MeasureTime frame
30-day composite endpoint incorporating mortality, persistent organ dysfunction (POD) in the ICU,13 ongoing hospital admissions, and discharge from the hospital with an increased level of care from baselineTimepoint: Day 30

Secondary

MeasureTime frame
the individual components of the composite described above, and the number of days without POD in the ICUTimepoint: Day 30

Countries

Australia, Canada, Denmark, India, New Zealand, United Kingdom

Contacts

Public ContactVignesh M

Dr Kamakshi Memorial Hospitals

vigneshm199@gmail.com9790158492

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Apr 4, 2026