Clinical Trial

Aspirin Discontinuation in High-Risk Pregnant Women of Preeclampsia

Unknown Phase 3
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Record status
This record was last updated July 3, 2024 (before its estimated December 30, 2024 completion). Its status may not reflect the trial's current state.
Summary
Low-dose aspirin (LDA) is considered to be the most effective agent to prevent preeclampsia (PE). At present, there is little exploration about the timing of aspirin discontinuation. Most international guidelines default until 36 weeks of gestation or delivery. China Guideline (2020) recommended that aspirin should be preventively used until 26-28 weeks of gestation, but there was little direct evidence. According to the two-stage theory, placental dysplasia before 28 weeks of gestation is the key to developing PE, the significance of aspirin use after 28 weeks of gestation is debatable. If aspirin discontinuation at 28 weeks of gestation is proven to be feasible for preventing preterm PE, it will not only reduce the risk of Perinatal Haemorrhage but also save medical expenses.
Protocol Amendment History 1 change
critical Trial status changed: Recruiting → Unknown 2026-08-02
Trial Details
NCT Number NCT06111079
Lead Sponsor FANG HE
Conditions Preeclampsia, Perinatal Haemorrhage
Enrollment 1,800 participants
Start Date 2023-11-01
Primary Completion 2024-12-30 (estimated)
Study Completion 2024-12-31 (estimated)
Updated on ClinicalTrials.gov 2024-07-03