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Effects of zoledronic acid for anti-osteoporosis therapy on blood lipid levels in patients with osteoporosis

Effects of zoledronic acid for anti-osteoporosis therapy on blood lipid levels in patients with osteoporosis

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2200055923
Enrollment
Unknown
Registered
2022-01-25
Start date
2022-02-01
Completion date
Unknown
Last updated
2024-07-22

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

Conditions

Osteoporosis

Interventions

Zoledronic acid treatment group:Nil
None zoledronic acid treatment group:Nil

Sponsors

Leshan People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
18 Years to 85 Years

Inclusion criteria

Inclusion criteria: 1. Inpatients with zoledronic acid for osteoporosis and those without zoledronic acid in the endocrinology department; 2. Men or women aged 18 to 85 years; 3. Voluntarily chose to participate in this clinical study.

Exclusion criteria

Exclusion criteria: 1. Patients with type 1 diabetes, type 2 diabetes, gestational diabetes, diabetes of unknown type, and special type of diabetes; 2. GFR sustained < 45mL/min/1.73^2, patients with severe renal impairment, end-stage renal disease or dialysis; 3. Women who are pregnant or breastfeeding, have had malignant tumor within 2 years and acute cerebrovascular accident within half a year; 4. Patients with abnormal thyroid function, hyperthyroidism, and hypothyroidism;

Design outcomes

Primary

MeasureTime frame
blood lipids;

Countries

China

Contacts

Public ContactLuo Wei

Leshan People's Hospital

Rainbowluowei@hotmail.com+86 13882722014

Outcome results

None listed

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