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Aspirin and Preeclampsia

StatusRecruiting
PhasePhase 4
Started
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Record History

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  1. Notable Primary completion date: Mar 1, 2026 to Dec 1, 2026v12
  2. Minor Primary completion date: Oct 1, 2025 to Mar 1, 2026
    • Study completion date: Dec 31, 2025 to Dec 31, 2026
    v11
  3. Minor 2 versions Re-verified since Jun 13, 2024, no change to tracked fieldsv9-v10
  4. Minor Primary completion date: Jan 1, 2026 to Oct 1, 2025
    • Study completion date: Feb 28, 2026 to Dec 31, 2025
    v8
  5. Minor Re-verified, no change to tracked fieldsv7
Show 5 earlier versionsHide 5 earlier versions
  1. Minor Secondary endpoints revised (5)
    • Study description expanded, about 4 words
    v6
  2. Minor Eligibility criteria expanded, about 30 wordsv5
  3. Notable Trial status: Not Yet Recruiting to Recruiting
    • Start date changed from estimate of Feb 1, 2021 to Feb 15, 2021
    • Site details revised
    v4
  4. Notable Start date: Sep 1, 2020 to Feb 1, 2021
    • Primary completion date: Jul 31, 2025 to Jan 1, 2026
    • Study completion date: Aug 31, 2025 to Feb 28, 2026
    v3
  5. Minor Secondary endpoints: details revised at 2 of 5 entriesv2
  1. Minor Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
This is a single-center, double-blind, randomized, placebo-controlled clinical trial. Peripartum and postpartum Activin A are significantly elevated in women with preeclampsia. Our hypothesis is that elevated Activin A levels reflect a remediable signal and that reducing postpartum Activin A levels with aspirin therapy will improve (GLS) in preeclamptic patients.
Trial Details
NCT Number NCT04479072
Lead Sponsor University of Chicago
Conditions
(from sponsor)
Preeclampsia Postpartum
Related terms Cardiovascular Diseases, Hypertension, Pre-Eclampsia
Enrollment 180 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov