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A retrospective analysis of the clinical efficacy of denosumab injections in the treatment of postmenopausal osteoporosis

A retrospective analysis of the clinical efficacy of denosumab injections in the treatment of postmenopausal osteoporosis

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2400090814
Enrollment
Unknown
Registered
2024-10-14
Start date
2024-10-16
Completion date
Unknown
Last updated
2024-10-21

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

Conditions

postmenopausal osteoporosis

Interventions

Denosumab injections Group:None
Control Group:None

Sponsors

Xi'an Honghui Hospital of Xi'an Jiaotong University
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
45 Years to 85 Years

Inclusion criteria

Inclusion criteria: The following criteria must all be met for trial inclusion: 1. Postmenopausal women aged between 45 and 85 years. 2. Conformance to the Western medicine diagnostic criteria for postmenopausal osteoporosis. 3. Those who have received at least two treatments of Denosumab injection. 4. Detailed records of initial and follow-up medical histories, along with comprehensive examination results. 5. Willingness to participate in this study.

Exclusion criteria

Exclusion criteria: To be eligible for the trial, all of the following criteria must be not met: 1.Patients with secondary osteoporosis. 2.Patients who are allergic to the study drug. 3.Patients with hypocalcemia. 4.Patients who participate in other clinical trials during the treatment period. 5.Any other conditions deemed inappropriate for the study by the investigator.

Design outcomes

Primary

MeasureTime frame
Bone mineral density;

Secondary

MeasureTime frame
ß-CrossLaps;Human N-terminal midfragmen of Osteocalcin;Serum Calcium 2+;Vitamin D;Parathyroid Hormone;Body Mass Index;

Countries

China

Contacts

Public ContactWang jun

Xi'an Honghui Hospital of Xi'an Jiaotong University

ttyy_163@163.com+86 134 6895 0290

Outcome results

None listed

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