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The clinical effect of teriparatide on BRONJ (bisphosphonate-related osteonecrosis of the jaw)

Not Applicable
Conditions
bisphosphonate-related osteonecrosis of the jaw
Registration Number
JPRN-UMIN000042862
Lead Sponsor
Kyushu Dental University
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete: follow-up complete
Sex
All
Target Recruitment
27
Inclusion Criteria

Not provided

Exclusion Criteria

Patients with hypercalcemia Patients who are considered to be at high risk of developing osteosarcoma as follows (a) Patients with Paget's disease of bone (b) Patients with unexplained high alkaline phosphatase levels (c) Young patients whose epiphyseal line has not yet closed (d) Patients who have received radiation therapy that may affect bone in the past. Patients with primary malignant bone tumors or metastatic bone tumors Patients with metabolic bone diseases other than osteoporosis (hyperparathyroidism, etc.) Pregnant women, women who may become pregnant, and lactating women Patients with a history of hypersensitivity to teriparatide components or teriparatide acetate Patients with serious complications such as cancer, cardiac disease, liver disease, and renal disorder Patients currently using an activated vitamin D preparation or a digitalis preparation Patients who are unable to give informed consent Patients who are judged by the physician to be unsuitable for teriparatide treatment

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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