Bone density.
Conditions
Interventions
Intervention group: These people will intervene after a bone density measurement test and confirmation of osteoporosis, if there is conscious consent,Individuals receive subcutaneous doses of 60 mg o
Sponsors
Deputy of research and technology of Alborz university of medical sciences
Eligibility
Sex/Gender
All
Age
18 Years to 60 Years
Inclusion criteria
Inclusion criteria: The patient should have informed consent to participate in the intervention The patient should be undergone hemodialysis courses The patient has a medical diagnosis of osteoporosis
Exclusion criteria
Exclusion criteria: The patient does not have conscious consent to participate in the intervention The patient does not have a medical diagnosis of osteoporosis The patient has a history of previous fractures
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Bone density. Timepoint: The amount of bone density will be measured before the intervention and one month after the subcutaneous injection of the prolia drug. Method of measurement: Bone density measurement test. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactElahe Dolatshahipirooz
Alborz University of Medical Sciences
Outcome results
None listed