Effects of Teriparatide Therapy for Japanese

Sponsor
Tomidahama Hospital (Other)
Overall Status
Unknown status
CT.gov ID
NCT01956461
Collaborator
(none)
500
1
85
5.9

Study Details

Study Description

Brief Summary

In this study, the investigators would like to analyze the bone mineral density (BMD) , bone turnover makers, and fracture prevention effects of daily teriparatide in Japanese patients under clinical practice. The participants are treated in the investigators hospital, who are under severe osteoporotic condition.

Several determinants were reported to be related to subsequent BMD increase, such as baseline bone turnover markers (BTMs), low BMD at baseline, age, prior treatment, but comprehensive discussion is lacking. Specifically, there analyses were performed fragmentarily.

The main objective of this study is to reveal the determinants of subsequent BMD increase and fracture preventing effect by teriparatide.

Next, in Japan, as the baby boom generation retires, aging and depopulation occur rapidly. As a result, there is a lot of nursing home. But there are few reports concerning to the efficacy of teriparatide treatment in nursing home patients. The second objective is to reveal the efficacy of teriparatide for patients living nursing home, especially BMD changes, bone turnover makers change, and adverse events.

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    Registry criteria: Patients treated in the investigators hospital using teriparatide. Enrolled patients are severe osteoporosis; more than two previous osteoporotic fractures, low BMD (< young adult mean 65%).

    Interventions: blood analyses and dual-energy X-ray absorptiometry (DXA) every 4 months Informed consent: Written informed consent will be obtained. Sample size: Five-hundreds participants

    Study Design

    Study Type:
    Observational [Patient Registry]
    Anticipated Enrollment :
    500 participants
    Observational Model:
    Case-Only
    Time Perspective:
    Prospective
    Study Start Date :
    Sep 1, 2010
    Anticipated Primary Completion Date :
    Nov 1, 2016
    Anticipated Study Completion Date :
    Oct 1, 2017

    Outcome Measures

    Primary Outcome Measures

    1. The determinants related to BMD increase and fracture prevention for teriparatide treatment [Up to 36 months]

      The investigators plan to analyze 500 patients who undergo teriparatide treatments 12 months. To enroll 500 participants, up to 24 months is required beside 12 months treatment periods. We investigate several determinants related to BMD increase, such as baseline age, gender, body mass index, BMD, BTMs, history of fracture, and prior treatment. We also investigate determinants related to fracture prevention effects by teriparatide treatment, such as baseline age, gender, body mass index, BMD, BTMs, history of fracture, prior treatment, walking ability, dementia,and site of living. To determine the response variables of BMD changes and fracture prevention effects, initially univariate analyses are performed by Spearman correlation coefficients and Mann-Whitney U test. Data are further analyzed with a multiple regression. To estimate odds ratios and 95% confidence intervals (95% CIs) of each determinants, logistic regression analyses are performed.

    Secondary Outcome Measures

    1. BMD and BTMs response, and fracture prevention effects of teriparatide for the patients in nursing home [Oct 2014]

      We plan to evaluate longitudinal BMD and BTMs changes for 24 months. BMD was evaluated every four months, ans BTMs are evaluated one months after treatment, and every four months. Fracture prevention effects are evaluated by radiography, if fracture is suspected. Statical analyses are performed using Spearman correlation coefficients, paired t-test, Mann-Whitney U test, and Kaplan-Meier method.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    45 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • severe osteoporotic patients
    Exclusion Criteria:
    • cancer, hypercalcemia, etc (i.e. patients who could not use teriparatide)

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Tomidahama Hospital Yokkaichi Mie Japan 510-8008

    Sponsors and Collaborators

    • Tomidahama Hospital

    Investigators

    None specified.

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Toshihiko Kono, Head of Hospital, Tomidahama Hospital
    ClinicalTrials.gov Identifier:
    NCT01956461
    Other Study ID Numbers:
    • IRB TH No 6
    First Posted:
    Oct 8, 2013
    Last Update Posted:
    Oct 19, 2016
    Last Verified:
    Oct 1, 2016
    Keywords provided by Toshihiko Kono, Head of Hospital, Tomidahama Hospital
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Oct 19, 2016