Clinical Trials Directory

Trials / Unknown

UnknownNCT05221164

162 mg of Aspirin for Prevention of Preeclampsia

Status
Unknown
Phase
Phase 4
Study type
Interventional
Enrollment
200 (estimated)
Sponsor
Methodist Medical Center of Illinois · Academic / Other
Sex
Female
Age
Healthy volunteers
Accepted

Summary

This is a study to assess if 162 mg of aspirin will decrease rates of preeclampsia in pregnant patients compared to 81 mg of aspirin.

Detailed description

After screening to meet inclusion criteria, pregnant patients at the Family Medicine Clinic will be asked to take 162 mg aspirin daily for 6 months, starting at about 12 weeks gestation and continued until the end of pregnancy. They will be monitored every 4 weeks until week 28, then every 2 weeks until week 36, and then weekly from week 36 on. Participants will be screened at these visits for medication compliance (taking, missed doses, side effects, etc). Patients will be subject to lab work as is routinely indicated for preeclampsia. At the end of the study period, accumulated study data will be compared with historical data from the Family Medicine Clinic on rates of preeclampsia and outcomes in patients taking 81 mg for preeclampsia prevention.

Conditions

Interventions

TypeNameDescription
DRUGAspirin 162 mgDaily aspirin 162 mg during pregnancy to prevent preeclampsia

Timeline

Start date
2021-07-06
Primary completion
2022-06-09
Completion
2022-06-09
First posted
2022-02-02
Last updated
2022-02-02

Locations

1 site across 1 country: United States

Regulatory

Source: ClinicalTrials.gov record NCT05221164. Inclusion in this directory is not an endorsement.