Skip to content

A retrospective study of zoledronic acid treatment in patients with primary osteoporosis—data from a 9-year osteoporosis patient management platform

A retrospective study of zoledronic acid treatment in patients with primary osteoporosis—data from a 9-year osteoporosis patient management platform

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2200060116
Enrollment
Unknown
Registered
2022-05-19
Start date
2022-05-07
Completion date
Unknown
Last updated
2024-04-22

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

Conditions

osteoporosis

Interventions

case series:None

Sponsors

Jiangxi Provincial People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
50 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Postmenopausal women or men aged over 50 years who have used zoledronic acid 5mg injection at least once for primary osteoporosis; 2. Patients diagnosed with osteoporosis according to the WHO diagnostic criteria for osteoporosis.

Exclusion criteria

Exclusion criteria: 1. Any bone disease other than primary osteoporosis; 2. Patients who received other bisphosphonate anti-osteoporosis drugs in the last 1 year before first zoledronic acid treatment, patients who used other anti-osteoporosis drugs in the last 6 months for more than 2 weeks: Teriparatide, estrogen, selective estrogen receptor modulator, strontium salt, or glucocorticoids in the last 6 months orally or intravenously for more than 3 months; 3. New diseases that affect bone metabolism after treatment with perzoledronic acid or drugs that affect bone metabolism.

Design outcomes

Primary

MeasureTime frame
Type 1 tropocollagen N - terminal propeptide;Type 1 procollagen carboxy-terminal peptide cross-linked peptide;Vitamin D;Blood calcium;Phosphorus in blood;Alkaline phosphatase;Bone density;

Countries

China

Contacts

Public ContactHuo Ya'nan

Jiangxi Provincial People's Hospital

hyn_hyn0216@126.com+86 13970029871

Outcome results

None listed

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