Osteoporosis, Postmenopausal Clinical Trial
— BRAVOOfficial title:
Quality of Life(QoL) in Korean Postmenopausal Osteoporosis Patients With Bisphosphonate Treatment
| Verified date | June 2017 |
| Source | GlaxoSmithKline |
| Contact | n/a |
| Is FDA regulated | No |
| Health authority | |
| Study type | Observational |
Quality of Life (QoL) in Korean postmenopausal osteoporosis patients with bisphosphonate treatment
| 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 |
| Country | Name | City | State |
|---|---|---|---|
| Korea, Republic of | GSK Investigational Site | Seoul |
| Lead Sponsor | Collaborator |
|---|---|
| GlaxoSmithKline |
Korea, Republic of,
| 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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