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Calcium Absorption in Postmenopausal Thai Women

C

Cornell University

Status

Completed

Conditions

Fractional Calcium Absorption

Study type

Observational

Funder types

Other

Identifiers

NCT02291315
IRB #: MU 2007-145

Details and patient eligibility

About

Adequate calcium absorption is essential for reducing one's risk of developing osteoporosis. However, postmenopausal Thai women consume diets which are habitually low in calcium due to lactose intolerance and dietary patterns which typically do not include milk-based products. The primary goal of this study is to measure the fractional calcium absorption from milk and a commonly ingested green leafy vegetable (cassia) in postmenopausal Thai women with habitually low calcium intakes. The secondary objective is to determine associations between calcium absorption and biomarkers which impact vitamin D status and bone metabolism.

Full description

Postmenopausal Thai women (n=22) will be recruited from the community surrounding Bangkok and Nakhon Pathon, Thailand. They will be invited to participate in an isotope study comparing the fractional calcium absorption from milk and cassia. Upon arrival, a fasting blood sample will be drawn on the morning of the absorption study to analyze serum markers of vitamin D and bone metabolism (25-hydroxy vitamin D [25OHD], parathyroid hormone [PTH], and beta-crossLaps) and to determine their impact on calcium absorption. Following this blood draw, women will receive a stable calcium isotope (42Ca) intravenously. Then for breakfast and lunch respectively, the women will be randomly assigned to orally ingest a stable calcium isotope from either the milk (44Ca) or cassia (43Ca) test meals. On day two, women will receive a breakfast, snack, and lunch meal. Urine samples will be collected over the entire 28 hour period and the 24-hr urine collection will be used to measure urinary calcium concentration and to calculate fractional calcium absorption.

Enrollment

22 patients

Sex

Female

Ages

53 to 65 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Healthy
  • At least 3 years postmenopausal

Exclusion criteria

  • Diagnosed gastrointestinal or metabolic diseases known to interfere with calcium absorption and metabolism
  • Women taking medications (including thiazide diuretics, hormonal replacement therapy, etc.) within two months prior to the study
  • Women taking dietary supplements within two months prior to the study

Trial design

22 participants in 1 patient group

Test meal ingestion
Description:
On the morning of the absorption study, fasted women received 2 mg of 42Ca intravenously (in 5 ml of isotonic saline) over 5 minutes before being randomly assigned to receive either the milk or cassia meal first for breakfast and the milk or cassia meal second for lunch. The milk meal consisted of approximately 100 mg of fresh ultrahigh temperature (UHT) milk to which 2 mg of 44Ca was added and allowed to equilibrate for 12 h prior to ingestion and the cassia meal consisted of 142 g of cooked cassia to which 1 mg of 43Ca was extrinsically added.

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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