Osteoporosis
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1)Female 2)Over 65 years old 3)Out patients 4)Primary osteoporosis with high risks of fragile fracture 5)Patients with sufficient informed consent to participate this study
Exclusion criteria
Exclusion criteria: 1)Patients with contraindication for the administration of teriparatide acetate 2)Patients who cannot drink a water orally 3)Patients who already had finished 104 times of the administration of teriparatide acetate, or were administrated several times 4)Patients who refused to participate this study by sufficient information 5)Other patients who are judged inappropriate to participate this study by director of this study
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The primary outcomes are the incidence of nausea after the administration of Teriparatide acetate. | — |
Secondary
| Measure | Time frame |
|---|---|
| The secondary outcomes are the change of blood pressures immediately after administration of Teriparatide acetate and persistence rate of the administration. | — |
Countries
Japan
Contacts
Kansai medical university, Kori Hospital Department of Orthopedic surgery