RecruitingPhase 4NCT03826524
Epinephrine Dose: Optimal Versus Standard Evaluation Trial
Studying Hereditary persistence of fetal hemoglobin-sickle cell disease syndrome
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- Unity Health Toronto
- Principal Investigator
- Paul Dorian, MD, MScUnity Health Toronto
- Intervention
- Epinephrine(drug)
- Enrollment
- 3790 target
- Eligibility
- 18 years · All sexes
- Timeline
- 2023 – 2028
Study locations (8)
- British Columbia Emergency Health Services (BCEHS), Victoria, British Columbia, Canada
- Peel Regional Paramedic Services, Brampton, Ontario, Canada
- Middlesex-London Paramedic Service, London, Ontario, Canada
- Halton Region Paramedic Services, Oakville, Ontario, Canada
- Ottawa Paramedic Services, Ottawa, Ontario, Canada
- Superior North Emergency Medical Services, Thunder Bay, Ontario, Canada
- Essex-Windsor Emergency Health Services, Windsor, Ontario, Canada
- Medavie Health Services West, Saskatoon, Saskatchewan, Canada
Collaborators
Canadian Institutes of Health Research (CIHR) · Pfizer
Primary source
Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.
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