CompletedNot applicableNCT03228082
Blood Pressure After PREeclampsia/HELLP by SELF Monitoring Study
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
- Radboud University Medical Center
- Principal Investigator
- A.H.E.M. Maas, Prof.dr.Radboudumc, department Cardiology
- Intervention
- Home Blood Pressure Monitoring (HBPM)(device)
- Enrollment
- 200 target
- Eligibility
- 40-60 years · FEMALE
- Timeline
- 2017 – 2019
Study locations (6)
- Katholisches Karl-Leisner-Klinikum GmbH, Kleve, Germany
- Krankenhaus Bethanien, Moers, Germany
- St. Josef Krankenhaus GmbH, Moers, Germany
- Rijnstate Ziekenhuis, Arnhem, Netherlands
- Radboudumc, Nijmegen, Netherlands
- Canisius-Wilhelmina Ziekenhuis, Nijmegen, Netherlands
Collaborators
Interreg
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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