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

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

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
TCTR
Registry ID
TCTR20221001001
Enrollment
222
Registered
2022-10-01
Start date
2021-05-19
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

Pregnant women with one or more high risk and women with two or more moderate risk of developing preeclampsia calcium carbonate pre-eclampsia prevention

Interventions

1250 mg of calcium carbonate tablet, taking three times a day starting at the enrollment or at 12 weeks of gestation,1250 mg of calcium carbonate tablet, taking once daily
High-dose calcium carbonate,Standard dose calcium carbonate

Sponsors

None listed

Eligibility

Sex/Gender
Female

Inclusion 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: 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.

Design outcomes

Primary

MeasureTime frame
Incidence of pre-eclampsia with severe features Until delivery Incidence

Secondary

MeasureTime frame
Incidence of pre-eclampsia without severe features Until delivery Incidence,Incidence of gestational hypertension Until delivery Incidence,Gestational age at delivery until delivery gestational age (weeks),Neonatal outcome until discharge Apgar, birthweight, NICU admission and length of stay,Adverse event until delivery constipation, nausea and vomiting, PPH

Countries

Thailand

Contacts

Public ContactPat Leelaamornvichet

Department of Obstetrics and Gynelocogy, Chonburi Hospital

mel_on.pat@hotmail.com0909821192

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 9, 2026