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Search / Trial NCT06281665

Treatment With Aspirin After Preeclampsia: TAP Trial

Launched by ALISSE HAUSPURG · Feb 19, 2024

Trial Information

Current as of June 26, 2025

Recruiting

Keywords

Hypertension

ClinConnect Summary

The TAP Trial is studying whether low-dose aspirin can help women recover better after experiencing preeclampsia, a serious pregnancy condition that can lead to high blood pressure and other complications. Researchers want to see if taking aspirin in the weeks after giving birth can improve blood vessel function and lower blood pressure for up to six months. The trial is currently looking to enroll up to 60 women who are at least 18 years old and have been diagnosed with preeclampsia.

If you join the study, you will have three visits where your blood pressure will be measured, and some blood tests will be done. You will also answer some questions about your health. The study will compare the effects of low-dose aspirin with a placebo (a sugar pill that has no effect) to see if the aspirin makes a difference. It’s important to note that women with certain conditions, like multiple pregnancies or allergies to aspirin, cannot participate. This trial aims to gather valuable information that could help improve care for women after preeclampsia.

Gender

FEMALE

Eligibility criteria

  • Inclusion Criteria:
  • Postpartum individuals ≥18 years old
  • Preeclampsia diagnosis
  • Exclusion Criteria:
  • Fetal anomaly
  • Multiple gestation
  • Pre-pregnancy hypertension
  • Allergy or contraindication to low-dose aspirin
  • Pre-pregnancy diabetes

About Alisse Hauspurg

Alisse Hauspurg is a dedicated clinical trial sponsor focused on advancing medical research and improving patient outcomes through innovative therapeutic solutions. With a commitment to excellence in clinical development, Hauspurg oversees a diverse portfolio of studies aimed at addressing unmet medical needs across various therapeutic areas. The organization collaborates with leading research institutions and healthcare professionals to ensure rigorous adherence to regulatory standards while promoting patient safety and ethical practices. By leveraging cutting-edge methodologies and fostering strong partnerships, Alisse Hauspurg strives to accelerate the delivery of transformative treatments to the market.

Locations

Pittsburgh, Pennsylvania, United States

Patients applied

0 patients applied

Trial Officials

Alisse K Hauspurg, MD

Principal Investigator

UPMC Magee Women's Hospital

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported