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Aspirin Dosing in Pregnancy

Aspirin Dosing and Platelet Phenotype in Pregnancy

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07525635
Enrollment
30
Registered
2026-04-13
Start date
2026-04-27
Completion date
2028-02-20
Last updated
2026-05-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Preeclampsia Possible

Keywords

Asprin, Pregnancy

Brief summary

The purpose of this study is assess platelet phenotypes based on aspirin dosing in pregnant patients at risk for the development preeclampsia who are taking 81mg twice a day aspirin. Blood samples will be collected approximately 4 weeks after initiation of aspirin to evaluate the platelet phenotype during pregnancy in patients.

Interventions

DRUGAspirin

81mg twice a day (162mg total)

Sponsors

NYU Langone Health
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 50 Years
Healthy volunteers
No

Inclusion criteria

* Pregnant people prior to 17 weeks * Prenatal care at NYU Langone Health Obstetrics and Gynecology Associates * Age 18-50 years * Singleton viable gestation * Pregnant patients at high risk of preeclampsia: Patients meeting USPSTF recommendation for aspirin prophylaxis for preeclampsia based on clinical risk factors.

Exclusion criteria

* Undergoing glucose challenge test (GCT) at time of blood draw * Allergy or intolerance to aspirin * Antithrombotic or antiplatelet therapy * Anemia (hemoglobin \<10 g/dl) or thrombocytopenia (platelet count \<100,000), or thrombocytosis (platelet count \>600,000) * Known hemorrhagic diathesis * Planned delivery outside of NYU

Design outcomes

Primary

MeasureTime frame
Measures of platelet aggregation assessed by Light Transmission Aggregometry (LTA)Baseline, 4 weeks after initiation of aspirin

Secondary

MeasureTime frameDescription
Change in serum thromboxaneBaseline, 4 weeks after initiation of aspirin
Change in complete blood countBaseline, 4 weeks after initiation of aspirin
Change in Mean Platelet Volume (MPV)Baseline, 4 weeks after initiation of aspirin
Change in Platelet Distribution Width (PDW)Baseline, 4 weeks after initiation of aspirin
Change in Plateletcrit (PCT)Baseline, 4 weeks after initiation of aspirin
Change in Life's Essential 8 questionnaireBaseline, 4 weeks after initiation of aspirinLife's Essential 8 (LE8) is a cardiovascular health scoring system from the American Heart Association that rates health from 0 to 100 based on diet, activity, smoking, sleep, BMI, cholesterol, blood sugar, and blood pressure. Scores indicate high cardiovascular health, 50-79 is moderate, and below 50 is low. A score of 100 is ideal, while 0 represents the lowest health condition, such as severe, uncontrolled risk factors.

Countries

United States

Contacts

CONTACTChristina A. Penfield, MD, MPH
Christina.Penfield@nyulangone.org646-754-2700
CONTACTLucia Muzzarelli
Lucia.Muzzarelli@nyulangone.org646-754-2760
PRINCIPAL_INVESTIGATORChristina A. Penfield, MD, MPH

NYU Langone Health

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: May 19, 2026