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Efficacy and safety of Bushen Tiaochong Recipe combined with alendronate sodium for treating postmenopausal senile degenerative osteoporosis

Efficacy and safety of Bushen Tiaochong Recipe combined with alendronate sodium for treating postmenopausal senile degenerative osteoporosis

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-IOR-17013947
Enrollment
Unknown
Registered
2017-12-15
Start date
2018-01-01
Completion date
Unknown
Last updated
2017-12-18

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

Conditions

postmenopausal senile degenerative osteoporosis

Interventions

1:alendronate sodium tablets and calcium carbonate D3 chewable tablets
2:alendronate sodium tablets, calcium carbonate D3 chewable tablets and Bushen Tiaochong Recipe

Sponsors

Affiliated Hospital of Qinghai University
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
55 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. In accordance with Guidelines for the diagnosis and treatment of primary osteoporosis (2011); 2. Kidney deficiency and blood stasis syndrome in accordance with Guiding principles of clinical study of new Chinese medicine; 3. Two years of natural menopause; 4. Signed informed consent.

Exclusion criteria

Exclusion criteria: 1. Metabolic bone disease, such as hyperthyroidism, diabetes, chronic kidney disease; 2. Sex hormone replacement therapy in nearly 3 months; 3. Severe heart, cerebrovascular, liver, kidney, and hematopoietic system diseases; 4. Mental illness; 5. Tumor disease; 6. Bone fracture; 7. Abnormal uterine bleeding.

Design outcomes

Primary

MeasureTime frame
Total efficacy;

Secondary

MeasureTime frame
Visual analogue scale scores for waist and back pain;L2-4 bone mineral density;Serological indicators;Incidence of adverse reactions;

Countries

China

Contacts

Public ContactMeige Qi

Affiliated Hospital of Qinghai University

meigege6797@163.com+86 13897436797

Outcome results

None listed

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