Evaluation of the efficacy of teriparatide for distal radial fracture repair after plate fixation in osteoporotic patients:A prospective randomized control study.

Not Applicable

• Conditions: osteoporosis

• Registration Number: JPRN-UMIN000015903
• Lead Sponsor: Yokohama City University Medical Center

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2015-01-01
• Study Completion: 2016-09-01
• Last Update Posted: 17 October 2023

Recruitment & Eligibility

• Status: Complete: follow-up complete
• Sex: All
• Target Recruitment: 20

Inclusion Criteria

Not provided

Exclusion Criteria

1)Primary malignant bone tumors or bone metastasis 2)Metabolic bone disease except primary osteoporosis 3)Under medication for osteoporosis(bisphosphonates, teriparatide, or SERM ) 4)Under medication of steroid 5)Hypercalcemia 6)Suspection of metal allergy 7)Dementia, Schizophrenia, Panic disorder and other diseases that may have affect the evaluation or obstruct obtaining consent

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Primary outcome is the comparison of the percent chage of bone mineral density (BMD)of the fracture site as measured by dual-energy x-ray absorptiometry(DEXA)with or without teriparatide administration from baseline to 24 weeks after surgery.

Secondary Outcome Measures

Name	Time	Method
Secondary outcome is the comparison of the percent change in markers of bone formation and resorption with or without teriparatide administration from baseline to 24 weeks after surgery.