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A randomized controlled exploratory study on the effects of different injection frequencies of teriparatide on bone metabolism in postmenopausal patients with hip fractures

A randomized controlled exploratory study on the effects of different injection frequencies of teriparatide on bone metabolism in postmenopausal patients with hip fractures

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600122353
Enrollment
Unknown
Registered
2026-04-13
Start date
2026-04-13
Completion date
Unknown
Last updated
2026-04-20

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

Conditions

Postmenopausal osteoporotic hip fracture

Interventions

Group A:Administer once daily. Teriparatide (20 µg per dose, administered once daily for three consecutive months)
Group B:Administer the drug twice a week. Teriparatide (28.5 µg per dose, twice a week, for a total of three months of continuous administration)

Sponsors

Peking University First Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
60 Years to 85 Years

Inclusion criteria

Inclusion criteria: 1. Age: 60 - 85 years (inclusive of the boundary value); 2. Fresh hip fractures after menopause confirmed by medical history and X-ray, and the time of fracture occurrence is = 20 ng/mL. If all other inclusion and exclusion criteria are met, the subjects can be given vitamin D and then re-tested; 5. PTH (15-65 pg/mL) and Ca (2.2-2.7 mmol/L) are within the normal detection range; 6. Fully capable of civil conduct, understanding the research process and methods, voluntarily participating in this trial, and signing the informed consent form in person.

Exclusion criteria

Exclusion criteria: 1. There are patients with bone metabolism disorders other than osteoporosis (such as osteomalacia, osteogenesis imperfecta, Paget's disease, Cushing's syndrome, hyperprolactinemia, etc.); 2. Before screening, they have used drugs that affect bone metabolism: within 2 years, they have used intravenous bisphosphonates, fluorides or strontium; within 6 months, they have used teriparatide or denosumab; the last oral bisphosphonate use was less than 1 year ago (excluding those with cumulative use 8.5%, severe arrhythmia); 8. Are allergic to teriparatide; 9. Are currently participating in other drug clinical trials; 10. There are other conditions that the investigator deems unsuitable for inclusion in the study.

Design outcomes

Primary

MeasureTime frame
Serum procollagen type I N-terminal propeptide (P1NP);Serum ß-type I collagen C-terminal peptide cross-linking (ß-CTX);Alkaline phosphatase (ALP);

Secondary

MeasureTime frame
Bone mineral density of lumbar spine and total hip;

Countries

China

Contacts

Public ContactCao Yongping

Peking University First Hospital

freehorse66@163.com+86 10 8357 2268

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Apr 23, 2026