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NCT06408181RecruitingPhase 3

APPLE: Aspirin to Prevent Pregnancy Loss and Preeclampsia

Source: ClinicalTrials.gov · Last updated 10 Sept 2026

Brief summary (registry, in English)

The goal of this clinical trial is to investigate the effects of early initiation of double low-dose aspirin in pregnant women. The main questions it aims to answer are: Does this dose and timing of aspirin reduce the risk of pre-eclampsia compared to standard recommendations? Does this dose and timing of aspirin reduce the risk of pregnancy loss compared to standard recommendations? Participants will begin taking at no later than 6 weeks 6 days gestational age, either 162mg of aspirin through delivery or placebo until 12 weeks and then 81mg of aspirin through delivery.

Status (registry)
Recruiting
Phase (registry)
Phase 3
Study type
Interventional
Enrollment
1150 (estimated)
First submitted
1 May 2024
Start date
12 Jun 2024
Primary completion date
30 Jun 2029
Lead sponsor
University of Pennsylvania
NCT number
NCT06408181

What you commit to

  • Study type: Interventional · Phase 3
  • Planned participants: 1150
  • From 12 Jun 2024 to the primary completion date, 30 Jun 2029
  • 1 site in 1 country
  • 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

  • Clinical indication for anticoagulant therapy, including prior or current thrombosis, antiphospholipid syndrome, or known major thrombophilia;

Other illness

  • Known allergies to aspirin. Exclusion to allergies to other non-steroidal anti-inflammatory agents (NSAID) will be determined on a case-by-case basis;
  • Medical contraindication to aspirin therapy, including untreated uncontrolled asthma, untreated symptomatic nasal polyps, bleeding disorders, or history of gastrointestinal ulcer.
  • Patients with pelvic pain or bleeding who require urgent care (i.e., active vaginal bleeding greater than or equal to expected menses, open cervical os suggesting active miscarriage or severe pain requiring evaluation for ectopic pregnancy)

Other

  • Clinical indication for chronic use of NSAIDS during pregnancy;

Who the study is looking for

  • Provision of signed and dated informed consent form.
  • Stated willingness to comply with all study procedures and availability for the duration of the study.
  • Ability to take oral medication and be willing to adhere to the prescribed aspirin regimen.
  • Patients with a gestation less than or equal to 6 weeks, 6 days (as determined by patient record of LMP or ART date).
  • Patients between 18-45-year old who have one or more risk factors for preeclampsia and/or pregnancy loss, including:
    • preeclampsia in a previous pregnancy,
    • gestational diabetes in a previous pregnancy,
    • any documentation of fetal growth restriction or low birth weight in a prior pregnancy,
    • preterm birth in a previous pregnancy,
    • known multifetal gestation at enrollment,
    • chronic hypertension,
    • pregestational diabetes,
    • kidney disease,
    • systemic lupus erythematosus,
    • nulliparity,
    • pre-pregnancy body mass index \>30,
    • family history of preeclampsia (i.e., mother or sister),
    • Black persons (due to social, not biological reasons),
    • Maternal age 35 years or older,
    • lower income (will be determined by qualification of public health insurance),
    • conceived with fertility treatment (including in vitro fertilization, ovulation induction, or intrauterine insemination),
    • history of one or more prior pregnancy losses \<20 weeks gestation,
    • history of stillbirth in a prior pregnancy,
    • An interval of greater than 10 years since the last pregnancy.

Age in the registry: 18 years to 45 years · Sex: Female · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

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

SiteCityCountrySite status
University of Pennsylvania
Coordinator of this site? Confirm its status
PhiladelphiaUnited StatesRecruiting

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