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Study identifier: NCT06494878 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

The PARTUM Trial: Postpartum Aspirin to Reduce Thromboembolism Undue Morbidity

Condition: Venous Thromboembolism · Postpartum Period · Aspirin  ·  Sponsor: University of Calgary

PhasePhase 3
Planned participants8805
Who can joinFemale, 18 Years to no upper limit
Healthy volunteersNo

About this study

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.

This description comes directly from the study's public registry record.

Talk to the study team

Leslie Skeith, MD  ·  403-944-5246  ·  laskeith@ucalgary.ca

Jill Baxter, BSc  ·  403-220-7103  ·  jbaxter@ucalgary.ca

Always discuss trial participation with your own doctor first.

Locations (12)

Association Hospitalière De Bruxelles Et De Schaerbeek - Centre Hospitalier Universitaire BrugmannBrussels, BelgiumNot Yet Recruiting
Foothills Medical CentreCalgary, Alberta, CanadaRecruiting
The Ottawa Hospital - General CampusOttawa, Ontario, CanadaNot Yet Recruiting
Hvidovre HospitalHvidovre, Capital Region, DenmarkNot Yet Recruiting
CHU de NancyNancy, FranceNot Yet Recruiting
APHP - Hôpital Port RoyalParis, FranceNot Yet Recruiting
CHU de Saint-EtienneSaint-Etienne, FranceNot Yet Recruiting
CHU de ToulouseToulouse, FranceNot Yet Recruiting
Rotunda Hospital, RCSI Department of Obstetrics and GynaecologyDublin, IrelandNot Yet Recruiting
UCD Centre for Human Reproduction, The Coombe HospitalDublin, IrelandNot Yet Recruiting
Amsterdam UMCAmsterdam, NetherlandsNot Yet Recruiting
Medical University of WarsawWarsaw, PolandNot Yet Recruiting

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Source record: clinicaltrials.gov/study/NCT06494878