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Comparison of Aspirin 75 mg versus 150 mg in preventing preeclampsia in high risk pregnant women

To compare the role of aspirin 75 mg vs aspirin 150 mg in prevention of pre eclampsia in patients at risk of developing pre eclampsia - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/04/108484
Enrollment
100
Registered
2026-04-15
Start date
Unknown
Completion date
Unknown
Last updated
2026-04-27

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

Conditions

Health Condition 1: O00-O9A- Pregnancy, childbirth and the puerperium

Interventions

Intervention1: Group A: Aspirin 75 mg: Women in this group will receive aspirin 75mg one tablet daily throughout the pregnancy and to stop taking tablets at 36 weeks of gestation or earlier in the eve

Sponsors

Dr RPGMC Kangra at Tanda
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Age more than equal to 18 years and less than equal to 40 years Singleton pregnancy Live fetus at the gestational age of 12 to 28 weeks High or moderate risk of developing pre eclampsia as per ACOG Atleast 1 high risk factor namely History of pre eclampsia Diabetes mellitus type 1 or 2 Chronic hypertension Chronic kidney disease Autoimmune disease Multi fetal gestation Combination of multiple moderate risk factors Or Atleast 2 or more of the following moderate risk factors including Obesity pre pregnancy BMI more than equal to 30 Advanced maternal age more than equal to 35 years Family history of pre eclampsia Nulliparity First degree relative with pre eclampsia Conception after in vitro fertilization

Exclusion criteria

Exclusion criteria: Allergy to aspirin Asthma Peptic ulcers History of alcohol or drug abuse within 6 months Previous registration in another drug trial within the previous 3 months

Design outcomes

Primary

MeasureTime frame
Prevention of pre eclampsia Timepoint: Before 34 weeks of gestation 34 to 36 weeks 6 days of gestation At or after 37 weeks of gestation

Secondary

MeasureTime frame
Comparison of feto maternal outcomes between the two groupsTimepoint: Before 37 weeks & after 37 weeks

Countries

India

Contacts

Public ContactDr Ajay Sood

Dr RPGMC Kangra at Tanda

chandelpreeti250299@gmail.com7018870498

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: May 1, 2026