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NCT Number: NCT05924971

Aspirin for Postpartum Patients With Preeclampsia

The purpose of this research study is to evaluate the effect of low-dose aspirin on recovery from severe preeclampsia (a high blood pressure disorder of pregnancy) among women who have given birth. We hypothesize that taking aspirin for the first week after giving birth will enhance recovery from preeclampsia by decreasing the levels of a protein called soluble fms-like tyrosine kinase (sFlt-1), which is thought to be a main contributor to the development of preeclampsia, and speeding up return to a normal blood pressure.

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Key information

Age range

18 year and older

Sex eligibility

Female

Study type

Interventional

Phase

Phase 2

Primary location

Miller Children's and Women's Hospital, Long Beach/MemorialCare Long Beach

Long Beach, California, 90740, United States

Location status: Recruiting

Location contact

Megan Oakes, MD

CONTACT

[email protected]

562-997-8510

About this study

Preeclampsia is a condition of the antenatal and postpartum periods, which manifests as new-onset hypertension and end-organ damage. Globally, preeclampsia is estimated to affect up to 9% of all pregnancies, though as many as two-thirds of patients who receive this diagnosis will remain hypertensive beyond the time of their postpartum hospital discharge. Because of this, postpartum preeclampsia is the leading cause of postpartum hospital readmission in the United States. Anti-hypertensive medications and magnesium sulfate are temporizing therapies aimed at preventing the immediate sequelae of preeclampsia such as seizures, stroke, and end-organ damage. However, there are no therapies directly targeting the pathophysiology underlying postpartum preeclampsia, which poses difficulties in promoting blood pressure recovery to a normotensive state.

Preeclampsia is considered a disorder of abnormal placentation, leading to the release of abnormal pro-angiogenic, anti-angiogenic, and vasoactive molecules. Specifically, excess elevations in anti-angiogenic proteins like soluble fms-like tyrosine kinase 1 (sFlt-1) relative to pro-angiogenic proteins like placental growth factor (PlGF) are thought to cause vasospasm and, in turn, hypertension. As such, it seems plausible that persistent postpartum sFlt-1 elevation is implicated in the pathophysiology of postpartum preeclampsia.

At low doses, acetylsalicylic acid, or aspirin, has been proven to target the aforementioned angiogenic imbalance by decreasing serum sFlt-1 levels. While aspirin is widely used during pregnancy to mitigate the risk of preeclampsia, the utility of aspirin in the postpartum period to target these pathways and promote BP recovery to a normotensive state is unknown. The central hypothesis of this trial is that use of aspirin in the first week postpartum will enhance recovery from preeclampsia by improving blood pressure recovery via decreased levels of sFlt-1.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Preeclampsia with severe features diagnosed during delivery admission, as defined by ACOG criteria.
  • Pre- and postnatal care provided by the Long Beach Memorial Ob/Gyn resident or Maternal-Fetal Medicine clinic.

Exclusion criteria

  • Patient age <18 years old
  • Non-English or Non-Spanish speaking
  • Chronic hypertension diagnosed before 20 weeks' gestation
  • Known allergy, prior adverse reaction, or any medical condition in which aspirin is contraindicated (nasal polyps, gastric or duodenal ulcers, history of gastrointestinal bleeding, severe hepatic dysfunction)
  • Aspirin prescribed postpartum for any other medical condition
  • Bleeding disorder
  • Breastfeeding an infant with thrombocytopenia

Treatment and study plan

Aspirin 81Mg Ec Tab

Drug

Aspirin 81 mg 1 tablet by mouth. Participants randomized to receive aspirin in addition to standard blood pressure management will receive the study medication nightly at 20:00, with first dose initiated within 24 hours of delivery.

Primary outcomes

  1. Reduction in sFlt-1

    Time frame: 1 week postpartum

    This outcome will determine the absolute change in sFlt-1, an anti-angiogenic protein implicated in the pathophysiology of preeclampsia.

Secondary outcomes

  1. Normotension (ACOG)

    Time frame: 1 week postpartum

    This outcome will measure the proportion of patients who achieve a blood pressure of <140/90, as defined by ACOG, without any further elevated values.

  2. Normotension (JNC)

    Time frame: 1 week postpartum

    This outcome will measure the proportion of patients who achieve a blood pressure of <130/80, as defined by JNC, without any further elevated values.

  3. Time to normotension

    Time frame: 6 weeks postpartum

    This outcome will assess the length of time in days to normotension after randomization. Normotension will be defined by both ACOG and JNC criteria.

  4. Anti-hypertensive therapy

    Time frame: 6 weeks postpartum

    This outcome will assess if additional or increased doses of anti-hypertensive therapies are needed following randomization.

  5. Readmission

    Time frame: 6 weeks postpartum

    This outcome will assess if a study participant is readmitted for blood pressure or preeclampsia related reasons following randomization.

  6. Adherence

    Time frame: 1 week postpartum

    This outcome will assess for adherence to aspirin therapy in those randomized to the aspirin arm. This is defined as greater than 90% consumption of the prescribed doses.

  7. Enrollment feasibility

    Time frame: 1 week postpartum

    This outcome will assess feasibility for future studies, defined as both the number of patients randomized by the number of patients eligible and the number of patients who completed the study protocol divided by the number of patients randomized.

  8. Postpartum hemorrhage

    Time frame: 6 weeks postpartum

    This safety outcome is defined as a postpartum hemorrhage of greater than 1 liter following randomization.

  9. Postpartum bleeding requiring intervention

    Time frame: 6 weeks postpartum

    This safety outcome is defined as postpartum bleeding requiring intervention (uterotonic administration, intrauterine balloon placement, dilation and curettage, or uterine artery embolization) following randomization.

  10. Unplanned postpartum evaluation for bleeding

    Time frame: 6 weeks postpartum

    This safety outcome is defined as the need for urgent evaluation for bleeding in the clinic/office, obstetrical triage unit, or emergency room for vaginal bleeding.

Study contacts

Contact information is provided by the study sponsor or research team.

Ashten B Waks, MD MSPH

CONTACT

[email protected]

562-997-8510

Megan C Oakes, MD MSCI

CONTACT

[email protected]

562-997-8510

Sponsors and collaborators

Lead sponsor

MemorialCare Health System

Other

Collaborators

  • University of California, Irvine

Registry information

Official study title

Acetylsalicylic Acid for Postpartum Preeclampsia: A Pilot Randomized Trial

Acronym: ASAPP

Important dates

Study start
2023
Primary completion
2026
Study completion
2026
First posted
Jun 29, 2023
Registry last updated
Jun 6, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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