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Exploration of individualized drug interval for zoledronic acid in the treatment of primary osteoporosis

Exploration of individualized drug interval for zoledronic acid in the treatment of primary osteoporosis

Status
Recruiting
Phases
Phase 4
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR1900021323
Enrollment
Unknown
Registered
2019-02-15
Start date
2019-02-20
Completion date
Unknown
Last updated
2019-02-18

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

Conditions

Primary osteoporosis

Interventions

First infusion of zoledronic acid:Zoledronic acid
Second infusion of zoledronic acid: Zoledronic acid

Sponsors

Department of Endocrinology and Metabolism, West China Hospital, Sichuan University
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: 1) elderly women after menopause; 2) Meet the diagnostic criteria for osteoporosis and diagnosed as osteoporosis; 3) indication of zoledronic acid medication; 4) Patients voluntarily participate in the trial, determine informed consent for drug interventions and indicators, are willing to bear the risk of medication and sign informed consent; 5) Can check and feedback according to the plan, and cooperate with the researcher of this topic.

Exclusion criteria

Exclusion criteria: 1) Those who do not meet the inclusion criteria; 2) Those who are allergic to any of the bisphosphonates or pharmaceutical ingredients; 3) People with various endocrine and metabolic diseases that cause secondary osteoporosis (such as hyperparathyroidism, diabetes, and other diseases that seriously affect bone or calcium metabolism; 4) Patients with severe liver and renal insufficiency and long-term glucocorticoid and immunosuppressive therapy 5) The patient has taken drugs that affect bone metabolism within 3 months. 6) patients with hypocalcemia, renal insufficiency and hypercalcemia patients; 7) Patients with malignant tumors; 8) severe liver disease, cirrhosis, severe heart failure, arterial calcification; 9) Clinical trial participants who have participated in other research drugs in the past four weeks; 10) Those who have poor compliance and cannot complete the test according to the research plan; 11) For any reason, the investigator believes that the subject is not suitable for the study.

Design outcomes

Primary

MeasureTime frame
Bone metabolism biochemical markers;

Secondary

MeasureTime frame
Clinical symptom score (degree of pain, mobility, coldness, grip);Bone density;

Countries

China

Contacts

Public ContactDecai Chen

Department of Endocrinology and Metabolism, West China Hospital, Sichuan University

18980601309@163.com+86 18980601309

Outcome results

None listed

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