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Study on the effect and mechanism of dairy products on the bone condition of postmenopausal women

Study on the effect and mechanism of dairy products on the bone condition of postmenopausal women

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200064825
Enrollment
Unknown
Registered
2022-10-19
Start date
2022-10-31
Completion date
Unknown
Last updated
2023-05-15

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

Conditions

Postmenopausal osteoporosis

Interventions

Experimental group:Drink high calcium fresh milk
Control group:Drink regular fresh milk

Sponsors

Beijing Ditan Hospital, Capital Medical University
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
40 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Women aged 40-75 years who have been postmenopausal for at least 1 year; 2. T score: t value is less than -1; 3. No symptoms of anorexia, intolerance or allergy to high calcium milk or other dairy products; 4. Stable living in Beijing and no plan to move out of Beijing in the past two years, stable eating habits, and able to cooperate with the completion of the research.

Exclusion criteria

Exclusion criteria: 1. Those who suffer from mental illness and cannot answer questions correctly or are unwilling to conduct questionnaires; those who cannot take care of themselves, cannot recall clearly and answer questions clearly, or have obvious movement disorders; 2. Suffering from any type of bone degenerative chronic disease (such as diabetes, kidney stones, remission of heart disease, cancer, hyperthyroidism and hypothyroidism, hyperparathyroidism, impaired kidney and liver function), history of traumatic fractures, Osteomalacia, renal osteodystrophy and other metabolic bone diseases or bone tumors; moderate or severe renal impairment (serum creatinine>2mg/dL or 177mmol/L), or abnormal liver function (ALT>2 times normal value) upper limit); moderate to severe chronic obstructive pulmonary disease; severe hypertension, cerebrovascular accident; 3. History of digestive system surgery, such as gastrectomy, fundoplication, colostomy, etc., or persistent vomiting or suspected digestive tract obstruction; 4. History of drug treatment, in the past 48 weeks, received hormone-related therapy to prevent postmenopausal diseases, or ingested anti-osteoporosis drugs and drugs that have an effect on bone metabolism, such as phenytoin, carbamazepine, etc.; or In the past 3 months, receiving drug treatment for the following diseases: cholecystitis, peptic ulcer, urinary tract infection, acute pyelonephritis, cystitis, hyperthyroidism and other abnormal thyroid function; 5. Patients with acute or chronic inflammatory diseases, or who are receiving antibiotics, probiotics, probiotics, or any other drugs that may affect the gut microbiota in the first 3 months of inclusion; 6. Suffering from infectious diseases such as tuberculosis and AIDS, and suffering from serious organic diseases, such as cancer, coronary heart disease, myocardial infarction and stroke; 7. Consuming other dietary supplements known to affect bone metabolism during treatment, including other milk, other soy milk, vitamin D, vitamin K, multivitamins and calcium tablets, etc., if this happens, they will be withdrawn from the group.

Design outcomes

Primary

MeasureTime frame
bone density;blood metabolites;

Countries

China

Contacts

Public ContactLiu Jun

Beijing Ditan Hospital, Capital Medical University

zhaojunying5183@dingtalk.com+86 18910005159

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026