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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01227369
Other study ID # 111720
Secondary ID
Status Completed
Phase N/A
First received June 3, 2010
Last updated June 6, 2017
Start date June 2008
Est. completion date November 2009

Study information

Verified date June 2017
Source GlaxoSmithKline
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Quality of Life (QoL) in Korean postmenopausal osteoporosis patients with bisphosphonate treatment


Description:

Cross-sectional quality of life survey using self-administered OPSAT-QTM questionnaire in Korean postmenopausal osteoporosis patients with bisphosphonate treatment


Recruitment information / eligibility

Status Completed
Enrollment 4376
Est. completion date November 2009
Est. primary completion date November 2009
Accepts healthy volunteers No
Gender Female
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Who have been diagnosed with postmenopausal osteoporosis by physician Who have received any oral bisphosphonates (weekly or monthly) at least for 2 months to provide answer of OPSAT-QTM questionnaire Who provide informed consent for study participation

Exclusion Criteria:

- Do not understand the contents of the questionnaire

Study Design


Related Conditions & MeSH terms


Intervention

Other:
OPSAT-Q
A linguistically validated Korean version of OPSAT-Q

Locations

Country Name City State
Korea, Republic of GSK Investigational Site Seoul

Sponsors (1)

Lead Sponsor Collaborator
GlaxoSmithKline

Country where clinical trial is conducted

Korea, Republic of, 

Outcome

Type Measure Description Time frame Safety issue
Primary Mean of composite satisfaction score (CSS) of OPSAT-QTM 0day
Secondary Mean of subscale satisfaction scores of OPSAT-QTM oday
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