162 mg of Aspirin for Prevention of Preeclampsia

Status Recruiting

Clinical Trial 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.

Clinical Trial 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. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT05221164
Study type	Interventional
Source	Methodist Medical Center of Illinois
Contact
Status	Recruiting
Phase	Phase 4
Start date	July 6, 2021
Completion date	June 9, 2022

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