UnknownNCT02305745
Determining the Risk Elevation After Maternity
Studying Preeclampsia
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
- Ottawa Hospital Research Institute
- Principal Investigator
- Dr Laura GaudetOttawa Hospital Research Institute
- Intervention
- Observational(other)
- Enrollment
- 55 target
- Eligibility
- 18 years · FEMALE
- Timeline
- 2015 – 2019
Study locations (1)
- The Ottawa Hospital, General Campus, Ottawa, Ontario, Canada
Collaborators
The Ottawa Hospital Academic Medical Association
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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