PRospective Evaluation of Peripartum Anticoagulation ManaGement for ThrOmboembolism
Venous Thromboembolism | Pregnancy RelatedThe PREP and GO study is an international multicentre prospective cohort evaluating anticoagulation management strategies around labor and delivery and the postpartum period.
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Conditions de participation
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Sexe:
FEMALE -
Âges admissibles:
18 to 60
Critères de participation
Inclusion Criteria:
* 18 years of age or older
* Requires anticoagulation during the antepartum period of pregnancy for a VTE indication, including at least one of:
1. Objectively confirmed VTE (DVT, superficial vein thrombosis \[SVT\], PE or unusual site thrombosis) diagnosed during the current pregnancy;
2. Objectively confirmed VTE diagnosed in a prior pregnancy;
3. Objectively confirmed VTE diagnosed when not pregnant;
4. Inherited or acquired thrombophilia requiring anticoagulation.
* Receiving any dose or type of LMWH during the antepartum period
Exclusion Criteria:
* Anticoagulation for a non-VTE indication, including prosthetic heart valves, atrial fibrillation, prevention of placenta-mediated pregnancy complications, or prevention of recurrent pregnancy loss (participants can be included with a diagnosis of antiphospholipid syndrome (APS) with or without thrombotic events)
* Unable to provide or declined consent.
* Home or birthing centre planned delivery.
Lieu de l'étude
Foothills Medical Centre
Foothills Medical CentreCalgary, Alberta
Canada
Contactez l'équipe d'étude
- Étude parrainée par
- University of Calgary
- Participants recherchés
- Plus d'informations
- ID de l'étude:
NCT05756244