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A prospective, randomized controlled study of elcatonin treatment for acute bone loss in perioperative period of fracture surgery

A prospective, randomized controlled study of elcatonin treatment for acute bone loss in perioperative period of fracture surgery

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500106599
Enrollment
Unknown
Registered
2025-07-25
Start date
2025-08-01
Completion date
Unknown
Last updated
2025-08-18

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

Conditions

Hip fracture

Interventions

Daily treatment group:Elcitonin injection 40IU, administered intramuscularly daily, until 2 weeks after the operation
Weekly treatment group:Elcitonin injection 20IU, administered intramuscularly once a week until 2 weeks after the operation
Control group:Conventional treatment (without calcitonin drugs), but standard perioperative bone health management is provided (including calcium and vitamin D supplementation, rehabilitation guidance

Sponsors

Peking Union Medical College Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
50 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Age over 50; 2. Hip fracture; 3. Braking is required for a certain period of time; 4. Newly diagnosed patients who have not received calcitonin treatment; 5. The liver, kidneys and other organ functions are good, and the patient can tolerate surgery and drug treatment. 6. Patients and their families can understand the research protocol and voluntarily participate in this study, and voluntarily sign the informed consent form.

Exclusion criteria

Exclusion criteria: 1. Hypocalcemia 2. Those who are allergic to or intolerant to elcitonin drugs; 3. Patients with allergic constitutions who are prone to rashes (erythema, rubella), etc. 4. Patients who have received calcitonin preparations or the bone resorption inhibitor bisphosphonate within the past three months; 5. Patients who concurrently use cardiac glycosides or calcium channel blockers during the treatment period; 6. Patients with bronchial asthma or a history of the disease; 7. Diseases or factors with abnormal clinical manifestations that need to be ruled out, including but not limited to diseases of the nervous system, cardiovascular system, kidneys, liver, gastrointestinal tract, respiratory system, metabolism, bones and other systems; 8. Participated in other clinical researchers in the past three months; 9. Have any other circumstances that the researcher deems unsuitable for inclusion.

Design outcomes

Primary

MeasureTime frame
Bone mineral density (BMD);

Secondary

MeasureTime frame
Bone turnover marker;Blood calcium level;24-hour urinary calcium level;Visual analogue scale,VAS;Sarcopenia score;The patients safety assessment ;

Countries

China

Contacts

Public ContactJia Zhang

Peking Union Medical College Hospital

zhangjiapumch@163.com+86 139 0116 6987

Outcome results

None listed

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