CompletedPhase 4NCT01352234
Comparison of Doses of Acetylsalicylic Acid in Women With Previous History of Preeclampsia
Studying Placental insufficiency
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
- CHU de Quebec-Universite Laval
- Principal Investigator
- Emmanuel Bujold, MD, MScCHU de Quebec-Universite Laval
- Intervention
- Acetylsalicylic Acid 160 mg(drug)
- Enrollment
- 104 target
- Eligibility
- 18 years · FEMALE
- Timeline
- 2011 – 2015
Study locations (1)
- Centre Hospitalier Universitaire de Québec (CHUQ)/Pavillon CHUL, Québec, Canada
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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