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The aim of this study is to examine the efficacy and adverse events in the following 3 groups in osteoporosis patients: 1. The administration period of teriparatide is less than 6 months and thereafter, denosumab for 24 months. 2. The administration period of teriparatide is from 6 to 12 months and thereafter, denosumab for 24 months. 3. The administration period of teriparatide is more than 12 months and thereafter, denosumab for 24 months.
Age
20 - 120 years
Sex
ALL
Healthy Volunteers
No
Yukio Nakamura
Matsumoto, Nagano, Japan
Start Date
October 9, 2018
Primary Completion Date
October 8, 2023
Completion Date
October 8, 2025
Last Updated
September 21, 2021
90
ESTIMATED participants
"Teriparatide", "Forteo® or Teribon"
DRUG
Lead Sponsor
Shinshu University
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.
View ClinicalTrials.gov Terms and ConditionsNCT07281586