Fact CheckerSign in

NCT06494878RecruitingPhase 3

The PARTUM Trial: Postpartum Aspirin to Reduce Thromboembolism Undue Morbidity

The PARTUM (Postpartum Aspirin to Reduce Thromboembolism Undue Morbidity) Trial

Source: ClinicalTrials.gov · Last updated 27 Jul 2026

Brief summary (registry, in English)

The goal of the PARTUM trial is to determine if taking low-dose aspirin daily for 6 weeks after delivery is similar (non-inferior) to usual care low-molecular-weight heparin injections to prevent venous thromboembolism (VTE: blood clots in the legs or lungs) for postpartum individuals with VTE risk factors.

Status (registry)
Recruiting
Phase (registry)
Phase 3
Study type
Interventional
Enrollment
8805 (estimated)
First submitted
12 Jun 2024
Start date
4 Jun 2026
Primary completion date
Sept 2030
Lead sponsor
University of Calgary
NCT number
NCT06494878

What you commit to

  • Study type: Interventional · Phase 3
  • Planned participants: 8805
  • From 4 Jun 2026 to the primary completion date, Sept 2030
  • 12 sites in 7 countries
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Received more than 1 dose of LMWH since delivery

Other illness

  • Need for postpartum LMWH prophylaxis or systemic anticoagulation as judged by their physician and/or local investigator. May include but is not limited to:
    • Documented history of provoked or unprovoked VTE
    • Mechanical heart valve(s)
    • Known antiphospholipid syndrome (APS)
    • Known high-risk inherited thrombophilia i) Antithrombin deficiency, or ii) Homozygous factor V Leiden, or iii) Homozygous prothrombin gene mutation, or iv) More than 1 thrombophilia: any combination of 2 or more: factor V Leiden, prothrombin gene mutation, protein C deficiency, protein S deficiency
  • Need for postpartum ASA as judged by their physician and/or local investigator. May include but is not limited to:
    • Documented history of myocardial infarction
    • Documented history of ischemic stroke or transient ischemic attack (TIA)
  • Active bleeding, excluding normal vaginal bleeding, at the time of randomization
  • Known medical condition as judged by their physician and/or local investigator to be a contraindication to ASA or LMWH including known ASA or LMWH allergy

Age

  • \<18 years of age

Other

  • More than 48 hours since delivery at the time of randomization
  • Unable or declined consent

Who the study is looking for

  • ONE (or more) First Order Criterion:
    • Known inherited thrombophilia diagnosed prior to enrolment, regardless of family history of VTE:
    • Heterozygous factor V Leiden, or ii. Heterozygous prothrombin gene variant, or iii. Protein C deficiency, or iv. Protein S deficiency, and/or
    • Antepartum immobilization for ≥7 days. Immobilization is defined as bed rest with 90% of waking hours spent in bed at any time during the antepartum period AND/OR
    • TWO (or more) Second Order Criteria:
  • Pre-pregnancy BMI ≥30 kg/m²
  • Smoking in the current pregnancy or within 3 months prior to pregnancy
  • Previous clinical history of superficial vein thrombosis
  • Preeclampsia
  • Current pregnancy ending in stillbirth (pregnancy loss \>20 weeks gestation)
  • Unplanned cesarean delivery (unplanned = not a scheduled cesarean delivery)
  • Small-for-gestational-age infant at time of delivery (\<3rd percentile adjusted for gestational age and sex)
  • Peripartum or postpartum infection (symptoms/signs of infection and documented fever and laboratory evidence of infection with positive blood cultures or an elevated white blood cell count based on local laboratory cutoffs)
  • Postpartum hemorrhage (≥1000 mL of blood loss, regardless of delivery mode)

Age in the registry: 18 years to - · Sex: Female · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (12)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Association Hospitaliere De Bruxelles Et De Schaerbeek Centre Hospitalier Universitaire Brugmann
Coordinator of this site? Confirm its status
BrusselsBelgiumNot yet recruiting
Foothills Medical Centre
Coordinator of this site? Confirm its status
CalgaryCanadaRecruiting
The Ottawa Hospital - General Campus
Coordinator of this site? Confirm its status
OttawaCanadaNot yet recruiting
Hvidovre Hospital
Coordinator of this site? Confirm its status
HvidovreDenmarkNot yet recruiting
CHU de Nancy
Coordinator of this site? Confirm its status
NancyFranceNot yet recruiting
APHP - Hôpital Port Royal
Coordinator of this site? Confirm its status
ParisFranceNot yet recruiting
Chu de Saint Etienne
Coordinator of this site? Confirm its status
Saint-EtienneFranceNot yet recruiting
CHU de Toulouse
Coordinator of this site? Confirm its status
ToulouseFranceNot yet recruiting
Rotunda Hospital, RCSI Department of Obstetrics and Gynaecology
Coordinator of this site? Confirm its status
DublinIrelandNot yet recruiting
UCD Centre for Human Reproduction, The Coombe Hospital
Coordinator of this site? Confirm its status
DublinIrelandNot yet recruiting
Amsterdam UMC
Coordinator of this site? Confirm its status
AmsterdamNetherlandsNot yet recruiting
Medical University of Warsaw
Coordinator of this site? Confirm its status
WarsawPolandNot yet recruiting

This page is information, not medical advice. Discuss any trial with your doctor.