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NCT03186131 Clinical Trial

Efficacy of Oral Ibandronate in Osteoporosis

Osteoporosis Clinical Trial

Official title:
Examination of Bone Metabolism and Bone Mineral Density in Primary and Secondary Osteoporosis Treated by Oral Ibandronate

Clinical Trial Details — Status: Recruiting

Administrative data
NCT number NCT03186131
Other study ID # Oral IBN2017
Secondary ID
Status Recruiting
Phase Phase 2
First received
Last updated
Start date October 12, 2017
Est. completion date June 8, 2025

Study information
Verified date September 2021
Source Shinshu University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

There has been no comparative data between oral ibandronate and oral ibandronate plus active vitamin D

Recruitment information / eligibility
Status Recruiting
Enrollment 100
Est. completion date June 8, 2025
Est. primary completion date December 8, 2022
Accepts healthy volunteers No
Gender All
Age group 20 Years and older
Eligibility Inclusion Criteria: - Osteoporotic patients who want to take oral ibandronate Exclusion Criteria: - Patients who are allergic to oral ibandronate or vitamin D Patients who have not taken oral ibandronate for the last 2 years

Study Design

Related Conditions & MeSH terms

Intervention

Drug:
• Ibandronate
To examine the efficacy of oral Ibandronate in osteoporosis
• Oral Ibandronate and Vitamin D
To examine the efficacy of oral Ibandronate and Vitamin D in osteoporosis

Locations
Country Name City State
Japan Yukio Nakamura Matsumoto Nagano

Sponsors (1)
Lead Sponsor Collaborator
Shinshu University

Country where clinical trial is conducted

Japan, 

Outcome
Type Measure Description Time frame Safety issue
Primary Bone mineral density Change from Baseline Values at 1 year
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