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Kefir on Bone Mineral Density and Bone Metabolism in Osteoporotic Patients

M

Ministry of Science and Technology, Taiwan

Status

Completed

Conditions

Osteoporosis

Treatments

Other: Kefir
Other: Placebo
Other: CaCO3

Study type

Interventional

Funder types

Other

Identifiers

NCT02361372
NSC-99-2324-B-005-017-CC1

Details and patient eligibility

About

In a controlled, parallel, double-blind intervention study over 6 months, the investigators investigated the effects of kefir-fermented milk (1,600 mg/kg) supplemented with calcium bicarbonate (CaCO3, 1,500 mg/kg) and bone metabolism in 40 osteoporosis patients, and compared them with CaCO3 alone without kefir supplements. Bone turnover markers were measured in fasting blood samples collected before therapy and at 1, 3, and 6 months. BMD values at the spine, total hip, and hip femoral neck were assessed by dual-energy x-ray absorptiometry (DXA) at baseline and at 6 months.

Enrollment

69 patients

Sex

All

Ages

55 to 70 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Clinical diagnosis of osteoporosis patients

Exclusion criteria

  • Any previous use of parathyroid hormone or sodium fluoride, use of anabolic steroids or growth hormone within 6 months before trial entry or oral or intravenous systemic corticosteroids within 12 months, and any previous use of strontium.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

69 participants in 2 patient groups, including a placebo group

Kefir and CaCO3
Experimental group
Description:
Kefir were administered 1,600 mg kefir-fermented milk per day and an accompanying supplement of 1,500 mg CaCO3 for 6 months
Treatment:
Other: Kefir
Placebo and CaCO3
Placebo Comparator group
Description:
Placebo and 1,500 mg of CaCO3 daily for 6 months
Treatment:
Other: Placebo
Other: CaCO3

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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