ASAPP: Aspirin for Postpartum Patients With Preeclampsia

Sponsor
MemorialCare Health System (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT05924971
Collaborator
University of California, Irvine (Other)
86
2
14.1

Study Details

Study Description

Brief Summary

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.

Condition or Disease Intervention/Treatment Phase
  • Drug: Aspirin 81Mg Ec Tab
Phase 2

Detailed Description

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.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
86 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
Patients with preeclampsia will be randomized after delivery to receive either standard blood pressure control plus aspirin 81 mg or standard blood pressure control alone.Patients with preeclampsia will be randomized after delivery to receive either standard blood pressure control plus aspirin 81 mg or standard blood pressure control alone.
Masking:
Single (Outcomes Assessor)
Masking Description:
The outcomes assessor will be blinded to study arms.
Primary Purpose:
Treatment
Official Title:
Acetylsalicylic Acid for Postpartum Preeclampsia: A Pilot Randomized Trial
Anticipated Study Start Date :
Jul 1, 2023
Anticipated Primary Completion Date :
Jul 1, 2024
Anticipated Study Completion Date :
Sep 1, 2024

Arms and Interventions

Arm Intervention/Treatment
Experimental: Standard blood pressure control plus aspirin 81 mg

Standardized postpartum blood pressure control Aspirin 81 mg by mouth x 1 week post-delivery

Drug: Aspirin 81Mg Ec Tab
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.

No Intervention: Standard blood pressure control

Standardized postpartum blood pressure control

Outcome Measures

Primary Outcome Measures

  1. Reduction in sFlt-1 [1 week postpartum]

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

Secondary Outcome Measures

  1. Normotension (ACOG) [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) [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 [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 [6 weeks postpartum]

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

  5. Readmission [6 weeks postpartum]

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

  6. Adherence [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 [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 [6 weeks postpartum]

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

  9. Postpartum bleeding requiring intervention [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 [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.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
Female
Accepts Healthy Volunteers:
No
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

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

  • MemorialCare Health System
  • University of California, Irvine

Investigators

  • Principal Investigator: Megan C Oakes, MD MSCI, Miller Children's and Women's Hospital, Long Beach/ MemorialCare Medical Center

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Megan Oakes, MD MSCI, MemorialCare Health System
ClinicalTrials.gov Identifier:
NCT05924971
Other Study ID Numbers:
  • 371-23
First Posted:
Jun 29, 2023
Last Update Posted:
Jun 29, 2023
Last Verified:
Jun 1, 2023
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
Yes
Studies a U.S. FDA-regulated Device Product:
No
Product Manufactured in and Exported from the U.S.:
Yes
Keywords provided by Megan Oakes, MD MSCI, MemorialCare Health System
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jun 29, 2023