Changes of Bone Turnover Markers and Bone Mineral Density After Osteoporosis Treatment

September 20, 2021 updated by: Yukio Nakamura, Shinshu University

Changes of Bone Turnover Markers and Bone Mineral Density After Treatment in Osteoporotic Patients

To examine the changes of bone mineral density and bone turnover markers after Bonviva treatment in osteoporotic patients

Study Overview

Status

Recruiting

Conditions

Intervention / Treatment

Study Type

Interventional

Enrollment (Anticipated)

100

Phase

  • Phase 4

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

  • Japan
    • Nagano
      • Komagane, Nagano, Japan, 399-4117
        • Recruiting
        • Showa Inan General Hospital

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

20 years to 100 years (Adult, Older Adult)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • Osteoporosis

Exclusion Criteria:

  • Kidney, parathyroid, congenital bone metabolic disease

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Treatment
  • Allocation: N/A
  • Interventional Model: Single Group Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Osteoporosis
Device: Ibandronic acid, vitamin D

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Changes of bone mineral density
Time Frame: every 4-6 months
To examine the changes of bone mineral density for the purpose of the effectiveness of the drug
every 4-6 months

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Improvement of bone turnover markers
Time Frame: Every 3-6 months
To examine the changes of bone turnover markers for the purpose of the effectiveness of the drug
Every 3-6 months

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Shinshu University

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

June 1, 2014

Primary Completion (Anticipated)

October 1, 2022

Study Completion (Anticipated)

December 1, 2025

Study Registration Dates

First Submitted

June 1, 2014

First Submitted That Met QC Criteria

June 3, 2014

First Posted (Estimate)

June 5, 2014

Study Record Updates

Last Update Posted (Actual)

September 21, 2021

Last Update Submitted That Met QC Criteria

September 20, 2021

Last Verified

September 1, 2021

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • IB2014

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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