Skip to content

PRospective Evaluation of Peripartum Anticoagulation ManaGement for ThrOmboembolism

Venous Thromboembolism | Pregnancy Related

The PREP and GO study is an international multicentre prospective cohort evaluating anticoagulation management strategies around labor and delivery and the postpartum period.

null

Participation Requirements

  • Sex:

    FEMALE
  • Eligible Ages:

    18 to 60

Participation Criteria

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.

Study Location

Foothills Medical Centre
Foothills Medical Centre
Calgary, Alberta
Canada

Contact Study Team

Primary Contact

Emily McKibbon

[email protected]
403-220-7631
Foothills Medical Centre
Foothills Medical Centre
Calgary, Alberta
Canada

Contact Study Team

Backup Contact

Leslie Skeith, MD

[email protected]
403-944-5246
Primary Contact

Emily McKibbon

[email protected]
403-220-7631
McMaster University Medical Centre
McMaster University Medical Centre
Hamilton, Ontario
Canada

Contact Study Team

Primary Contact

Jessica Murphy

[email protected]
905-525-9140
CHU Sainte-Justine
CHU Sainte-Justine
Montreal, Quebec
Canada

Contact Study Team

Primary Contact

Hasna Meddour

[email protected]
BC Women's Hospital and Health Centre
BC Women's Hospital and Health Centre
Vancouver, British Columbia
Canada

Contact Study Team

Primary Contact

Simran Singh

[email protected]
Montfort Hospital
Montfort Hospital
Ottawa, Ontario
Canada

Contact Study Team

Primary Contact

Christine-Nadia Compas

[email protected]
613-746-4621
St. Boniface Hospital
St. Boniface Hospital
Winnipeg, Manitoba
Canada

Contact Study Team

Primary Contact

David Kent

[email protected]
204-237-2985
Mount Sinai Hospital
Mount Sinai Hospital
Toronto, Ontario
Canada

Contact Study Team

Primary Contact

Natasha Milligan

[email protected]
Royal Alexandra Hospital
Royal Alexandra Hospital
Edmonton, Alberta
Canada

Contact Study Team

The Ottawa Hospital - General Campus
The Ottawa Hospital - General Campus
Ottawa, Ontario
Canada

Contact Study Team

The Sir Mortimer B. Davis Jewish General Hospital
The Sir Mortimer B. Davis Jewish General Hospital
Montreal, Quebec
Canada

Contact Study Team

Study Sponsored By
University of Calgary
Participants Required
More Information
Study ID: NCT05756244