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Clinical Trials in Canada / NCT04923984
Recruiting Not applicable

Embolization of Middle Meningeal Artery for Subdural Hematoma in Canada (EMMA Can)

NCT04923984 · tracked via the Priya Life Science Canada tracker
Phase
Not applicable
Started
2021-05-01
Last updated
2026-02-03

Condition(s) studied

Subdural Hematoma

Investigational drug(s) / intervention(s)

Embolization of the middle meningeal artery

Embolization of the middle meningeal artery: embolization of the middle meningeal artery with an embolic agent (Microparticles, liquid embolic agents, SwiftPAC coils or others).

Study summary

EMMA-Can is a prospective cohort study to assess the safety and effectiveness of MMA-embolization for the treatment of CSDH.

Hypothesis- EMMA reduces the recurrence rate of CSDH with or without concomitant surgical evacuation.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: \- All patients with subdural hematoma coming to the emergency room or to neurosurgical outpatient clinic. Exclusion Criteria: * If informed consent cannot be obtained from the patient or their substitute decision maker. * Known allergy to liquid embolic agent

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Health Sciences centre Winnipeg MB Manitoba Recruiting

More University of Manitoba trials in Canada

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT04923984 on ClinicalTrials.gov ↗ ← All trials in Canada