Can a smaller calcium dose do the same job in pregnancy?
NCT ID NCT07784218
First seen Aug 25, 2026 · Last updated Aug 26, 2026 · Updated 1 time
Summary
This trial asks whether a lower daily calcium dose (300 mg) can match the standard higher dose (600 mg) in supporting bone health during pregnancy. Pregnant women between 22 and 28 weeks of gestation will be randomly assigned to one of the two doses. Researchers will measure changes in bone density, blood calcium levels, and urine calcium to see if the lower dose is enough. They will also track side effects like constipation and check for any impact on pregnancy outcomes such as preeclampsia or preterm birth.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Calcium supplement (300 mg/day vs 600 mg/day)
- What this could lead to
- If a lower calcium dose works as well as the standard one, it could reduce side effects like constipation and kidney strain while keeping bones and pregnancy healthy.
- What could go wrong
- This is a small pilot study, so results may not apply to all pregnancies. Lower calcium might not protect bone density or prevent complications as effectively as the higher dose.
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Study facts
What this study's own registry entry says, in plain language.
- Phase
-
Phase 4
Runs after approval, following long-term safety and how well the treatment works in everyday use.
- Participants
-
117 people
The number who actually took part.
- Started
-
Sep 2025
- Finished
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Jul 2026
- Lead sponsor
-
Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
-
14 to 45 years
- Sex
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Female participants only
- Healthy volunteers
-
Accepted
You do not need to have the condition being studied to take part.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Pregnant women aged 18 to 45 years * Gestational age between 22 and 28 weeks * Body mass index (BMI) between 19.0\~28.0 kg/m2 * Willingness to comply with the study protocol and provision of informed consent Exclusion Criteria: * Known hypersensitivity or allergy to any active components or excipients of the study medications * Multifetal gestation * History of chronic constipation or functional defecation disorders prior to or during early pregnancy * Current clinical hypercalcemia, hyperuricemia, familial hyperlipidemia, or intestinal malabsorption disorders * History of prolonged extreme low-calcium diets or severe diagnosed nutritional deficiencies * History of illicit substance abuse, chronic alcoholism, heavy smoking, or excessive caffeine intake
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As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Hangzhou First People's Hospital
Hangzhou, China
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