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Completed
NCT07852585
Comparison of Pregnancy Outcomes in Primigravida Receiving Low-Dose Aspirin for the Prevention of Preeclampsia.
Conditions: Preeclampsia
Sex: Female
Ages: 18 Years – 40 Years
Healthy volunteers: No
Phase: NA
Enrollment: 160
Sponsor: Muhammad Aamir Latif
Location: Bahawal Victoria Hospital/Quaid-e-Azam Medical College Bahawalpur Punjab Province
Summary
Local data on the effectiveness of low-dose aspirin in high-risk primigravida are limited. The present study was planned to compare pregnancy outcomes between high-risk primigravida receiving low-dose aspirin (75 mg/day) from 12 weeks of gestation and those not receiving aspirin.
Eligibility Criteria
Inclusion Criteria:
* Primigravida women
* High-risk pregnancy
* Aged 18-40 years
* Singleton pregnancy
* Gestational age ≤12 weeks
Exclusion Criteria:
* Women with pre-existing chronic hypertension
* Renal disease
* Diabetes mellitus
* Autoimmune disease
* Bleeding disorders
* Hypersensitivity to aspirin
* History of peptic ulcer disease
* Those using aspirin or other antiplatelet drugs
Source: ClinicalTrials.gov (NCT07852585). StuddyBuddy aggregates publicly available trial information.
