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Clinical Trials/TCTR20221001001
TCTR20221001001
Terminated
Phase 3

Calcium and Aspirin Supplementation for Prevention of Preeclampsia (in High Risk Pregnancy)

/A0 sites130 target enrollmentOctober 1, 2022

Overview

Phase
Phase 3
Intervention
Not specified
Conditions
Pregnant women with one or more high risk and women with two or more moderate risk of developing preeclampsia
Sponsor
/A
Enrollment
130
Status
Terminated
Last Updated
last year

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
October 1, 2022
End Date
April 5, 2022
Last Updated
last year
Study Type
Interventional
Sex
Female

Investigators

Sponsor
/A

Eligibility Criteria

Inclusion Criteria

  • Those who have one or more high\-risk or two or more moderate risks of developing pre\-eclampsia High risk of developing pre\-eclampsia was defined as a pregnant woman with multifetal gestation, chronic hypertension, type 1 or type 2 diabetes, renal disease, autoimmune disease (e.g., systemic lupus erythematosus and antiphospholipid syndrome), and a history of pre\-eclampsia. Moderate risk was defined as women with nulliparity, obesity with body mass index more than 30 kg/m2, family history of pre\-eclampsia, age 35 years or older, personal history factors (e.g., low birthweight or small for gestational age, previous adverse pregnancy outcome, more than 10\-year pregnancy interval)

Exclusion Criteria

  • Exclusion criteria were patients with a history of kidney or ureteric stone, parathyroid disorders, untreated nasal polyp, aspirin\-induced bronchospasm, gastrointestinal or urinary hemorrhage, severe liver disease, hypercalcemia (serum corrected calcium level more than 10\.5 mg/dL), allergic to aspirin or CaCO3, and other underlying diseases already receiving aspirin or calcium supplementation.

Outcomes

Primary Outcomes

Not specified

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