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Comparative study of zoledronic acid and alendronate in the treatment of postmenopausal osteoporosis

Comparative study of zoledronic acid and alendronate in the treatment of postmenopausal osteoporosis

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100045485
Enrollment
Unknown
Registered
2021-04-17
Start date
2021-05-31
Completion date
Unknown
Last updated
2021-11-29

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

Conditions

Postmenopausal osteoporosis

Interventions

Alendronate Group:Alendronate 70mg/week orally
Zoledronic acid :Zoledronic acid 5mg/year intravenously

Sponsors

The First Affiliated Hospital of Xi 'an Jiaotong University
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
50 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Women's natural menopause time >= 2 years; 2. In line with the 2020 AACE/ACE "Diagnosis and Treatment of Postmenopausal Osteoporosis" guidelines, all patients have undergone dual-energy X-ray absorptiometry to determine the lumbar spine (front and back), femoral neck, total hip joint or distal radius 1 3 Bone mineral density T value <=2.5.

Exclusion criteria

Exclusion criteria: 1. Long-term use of glucocorticoids; 2. Use bisphosphonates, calcitonin and other drugs that affect bone metabolism within 1 year before enrollment; 3. Suffer from diseases that affect bone metabolism, such as diabetes, multiple myeloma, rheumatic diseases, thyroid and parathyroid diseases, etc.; 4. Patients with tumors and abnormal immune function; 5. Severe pathological changes in important organs such as heart, liver, kidney and brain, including: estimated eGFR < 35mL /min, liver cirrhosis, etc.; 6. Patients with mental disorders who do not cooperate with treatment; 7. Patients who are allergic to the test drug; 8. Patients who are contraindicated with the test drug: patients with hypocalcemia, pregnant women, breastfeeding women, esophageal abnormalities that cause delay in emptying of the embassy, such as esophageal stenosis, patients who cannot stand or sit upright for at least 30 minutes.

Design outcomes

Primary

MeasureTime frame
total hip joint T value;Bone trabecular fraction of Lumbar spine;N-terminal propeptide of type I procollagen;ß cross-linked C-telopeptide of type 1 collagen;

Countries

China

Contacts

Public ContactCui Wei

The First Affiliated Hospital of Xi'an Jiaotong University

doctorweiwei.cui@126.com+86 18991232462

Outcome results

None listed

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