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NCT06281665: TAP
Treatment With Aspirin After Preeclampsia: TAP Trial
Phase 4 trial testing Low-dose aspirin in Hypertensive Disorder of Pregnancy in 60 participants. Currently enrolling.
1 June 2026
Quick facts
| Lead sponsor | Malamo Countouris |
|---|---|
| Phase | Phase 4 |
| Status | Recruiting now |
| Study type | INTERVENTIONAL |
| Allocation | randomized |
| Design | parallel |
| Masking | triple |
| Primary purpose | other |
| Enrollment | 60 |
| Start date | 29 May 2024 |
| Primary completion | 1 June 2026 |
| Estimated completion | 1 June 2027 |
| Sites | 1 location across United States |
Drugs / interventions tested
- Low-dose aspirin
- Placebo
Conditions studied
- Hypertensive Disorder of Pregnancy — all drugs for Hypertensive Disorder of Pregnancy →
- Pre-Eclampsia — all drugs for Pre-Eclampsia →
- Hypertension — all drugs for Hypertension →
- Eclampsia — all drugs for Eclampsia →
Sponsor
Malamo Countouris
Who can join
Adults 18 to 55, female only, with Hypertensive Disorder of Pregnancy or Pre-Eclampsia. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
The objective of this research project is to conduct a single-site pilot trial to assess the feasibility and effect of low-dose aspirin to augment vascular recovery in the immediate postpartum period after preeclampsia through two specific aims: 1) to pilot test the feasibility of conducting a randomized controlled trial of postpartum low dose aspirin vs. placebo, and 2) to assess the effect of postpartum aspirin on endothelial function and blood pressure. Our central hypothesis is that postpartum administration of low-dose aspirin following preeclampsia will be feasible, improve endothelial function, and lower BP at 6 months postpartum. Subjects will undergo 3 study visits involving BP measurements, blood draws, questionnaires, and/or microiontophoresis. Up to 60 adult subjects will be enrolled at Magee-Women's Hospital.
Publications & conference data
No peer-reviewed publications indexed yet for this trial.
Verify or expand the search:
- PubMed search for NCT06281665
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
Related trials
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Trials testing the same drug.
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- NCT05198960 — AVAJAK: Apixaban/Rivaroxaban Versus Aspirin for Primary Prevention of Thrombo-embolic Complications in JAK2V617F-positiv · Phase 3 · recruiting
- NCT05089175 — The Investigation of the Prediction Model and Prevention Strategy of Serious Pregnancy Complications in Hypertensive Dis · unknown
Other recruiting trials for Hypertensive Disorder of Pregnancy
Currently open trials in the same condition.
- NCT07405723 — Arm Position and Blood Pressure Measurement Accuracy During Pregnancy · NA · recruiting
- NCT07204756 — HOPE-BP 2.0: Evaluating the Optimal Duration of Postpartum Remote Blood Pressure Monitoring · NA · recruiting
- NCT06362356 — Microbial Metabolites and Outcomes of Pregnancy Study · active not recruiting
- NCT05655936 — Eliminating Severe Maternal Morbidity With Heart Health Doulas Trial · NA · recruiting
- NCT05659173 — Vitamin D Deficiency With Selected Vitamin D Receptor Gene Polymorphism in Gestational Hypertension · active not recruiting
Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT06281665 (US National Library of Medicine, public domain)
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by Malamo Countouris
- Last refreshed: 5 February 2026
Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT06281665.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing