RecruitingPhase 2NCT05924971

Aspirin for Postpartum Patients With Preeclampsia

Acetylsalicylic Acid for Postpartum Preeclampsia: A Pilot Randomized Trial


Sponsor

MemorialCare Health System

Enrollment

86 participants

Start Date

Jul 26, 2023

Study Type

INTERVENTIONAL

Conditions

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.


Eligibility

Sex: FEMALEMin Age: 18 Years

Inclusion Criteria2

  • 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 Criteria7

  • 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

Interventions

DRUGAspirin 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.


Locations(1)

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

Long Beach, California, United States

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NCT05924971


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