Aspirin Dosage Comparison for Preeclampsia Prevention in High-Risk Pregnancies
This study observes if different aspirin dosages can prevent preeclampsia in high-risk pregnancies, tracking both early and late onset of the condition.
Aspirin 75 mg
+ Aspirin 150 mg
Urogenital Diseases+2
+ Female Urogenital Diseases and Pregnancy Complications
+ Pre-Eclampsia
Prevention Study
Summary
Study start date: November 1, 2025
Actual date on which the first participant was enrolled.This study focuses on finding the best dose of Aspirin to help prevent pre-eclampsia in pregnant women who are at high risk for this condition. Pre-eclampsia is a serious condition that can affect both the mother and the baby, potentially leading to complications during pregnancy. It occurs in 5-7% of all pregnancies and can be life-threatening. Aspirin is known to help prevent pre-eclampsia by improving blood flow to the placenta and reducing inflammation and blood clot formation. This study aims to compare two different doses of Aspirin, 75mg and 150mg, to see which is more effective in the Pakistani population, as different guidelines exist on the appropriate dose for prevention of pre-eclampsia. Participants in this study will take either 75mg or 150mg of Aspirin daily from early in their pregnancy, starting at 12 weeks. Researchers will monitor the participants to see if they develop pre-eclampsia, and if so, whether it occurs early or later in the pregnancy. The outcomes will be measured by checking whether pre-eclampsia develops before or after 34 weeks of pregnancy. The study will help determine if a higher dose of Aspirin is more effective in preventing pre-eclampsia, potentially leading to improved care for pregnant women at risk of this condition. The main focus is on assessing whether the benefits of preventing pre-eclampsia outweigh any potential side effects of taking a higher dose of Aspirin.
Protocol
This section provides details of the study plan, including how the study is designed and what the study is measuring.340 patients to be enrolled
Total number of participants that the clinical trial aims to recruit.Prevention Study
Eligibility
Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.Female
Biological sex of participants that are eligible to enroll.From 18 to 30 Years
Range of ages for which participants are eligible to join.Healthy volunteers not allowed
If individuals who are healthy and do not have the condition being studied can participate.Conditions
Pathology
Criteria
Study Plan
Find out more about all the medication administered in this study, their detailed description and what they involve.2 intervention groups are designated in this study
This study does not include a placebo group
Treatment Groups
Group I
ExperimentalGroup II
ExperimentalStudy Objectives
Primary Objectives
Secondary Objectives
Study Centers
These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.This study has 1 location