| Primary | Percentage of Participants Current Daily or Weekly Bisphosphonate Users in Part A Who Answer 'Yes' to Any of the Questions in the Candidate Identification Questionnaire (CIQ) | The CIQ was completed in Part A by all the participants. The information from the CIQ was used to determine the percentage of current daily or weekly bisphosphonate users for whom monthly ibandronate represented a potentially more satisfactory therapeutic option. In the CIQ participants were asked to answer either 'yes' or 'no' to the following 3 questions:
- I would prefer a monthly oral dosing schedule to my current (daily or weekly) dosing schedule.
- More than once per month, I have experienced stomach upset within 48 hours of taking my osteoporosis medication.
- Over the past 3 months, I have missed taking 3 or more doses of my current (daily or weekly) osteoporosis medication.
| All enrolled participants who completed the part A of the study. | Posted | | Number | | percentage of participants | | Visit 0 (less than or equal to [<=] Day -30) | | | | ID | Title | Description |
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| OG000 | Ibandronate | Participants completed Candidate Identification Questionnaire (CIQ) in Part A and received Ibandronate 150 milligram (mg) tablet orally once-monthly up to 6 months in Part B of the study. |
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| Primary | Percentage of Participants Who Reported Preference for Monthly Ibandronate | Percentage of participants who reported preference for monthly ibandronate were reported. | All enrolled participants who completed the part A of the study. | Posted | | Number | | percentage of participants | | Visit 0 (<= Day -30) | | | | ID | Title | Description |
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| OG000 | Ibandronate | Participants completed Candidate Identification Questionnaire (CIQ) in Part A and received Ibandronate 150 milligram (mg) tablet orally once-monthly up to 6 months in Part B of the study. |
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| Primary | Percentage of Participants With Positive Change in Total Composite Satisfaction Score (CSS) at Month 6 in Part B by CIQ Fracture (Fr) Group | Participants with a positive change from their baseline CSS at Month 6 are considered those participants who are satisfied with once-monthly dosing of ibandronate after 6 months of use were reported. The CSS is scaled from 0 to 100 and is an average of the 4 domain scores of the Osteoporosis Patient Satisfaction Questionnaire (OPSAT-Q): Convenience (questions 1 to 6), Quality of Life (questions 7 and 8), Overall Satisfaction (questions 9 and 10) and Side Effects (questions 11 to 16). Higher scores indicating greater satisfaction. | The intent-to treat (ITT) population included all participants who received at least one dose of study medication. Number of participant analyzed are with or without previous history of Fr. | Posted | | Number | | percentage of participants | | Month 6 | | | | ID | Title | Description |
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| OG000 | Ibandronate | Participants completed Candidate Identification Questionnaire (CIQ) in Part A and received Ibandronate 150 milligram (mg) tablet orally once-monthly up to 6 months in Part B of the study. |
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| Secondary | Percentage of Participants Eligible Current Daily or Weekly Bisphosphonate Users at Screening Who Elect to Enter Part B by CIQ | | The ITT population included all participants who received at least one dose of study medication. | Posted | | Number | | percentage of participants | | Visit 0 (<= Day -30) | | | | ID | Title | Description |
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| OG000 | Ibandronate | Participants completed Candidate Identification Questionnaire (CIQ) in Part A and received Ibandronate 150 milligram (mg) tablet orally once-monthly up to 6 months in Part B of the study. |
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| Secondary | Percentage of Participants Who Reported an Improved Satisfaction Score After 6 Months in Part B | Percentage of participants who report an improved satisfaction score after 6 months of monthly ibandronate therapy as compared to daily or weekly alendronate or risendronate at baseline based on responses to each individual question in the CIQ were reported. In the CIQ participants were asked to answer either 'yes' or 'no' to the following 3 questions:
- I would prefer a monthly oral dosing schedule to my current (daily or weekly) dosing schedule
- More than once per month, I have experienced stomach upset within 48 hours of taking my osteoporosis medication
- Over the past 3 months, I have missed taking 3 or more doses of my current (daily or weekly) osteoporosis medication
| The ITT population included all participants who received at least one dose of study medication. | Posted | | Number | | percentage of participants | | Month 6 | | | | ID | Title | Description |
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| OG000 | Ibandronate | Participants completed Candidate Identification Questionnaire (CIQ) in Part A and received Ibandronate 150 milligram (mg) tablet orally once-monthly up to 6 months in Part B of the study. |
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| Secondary | Percentage of Participants Who Have Greater Than or Equal to (>=) 80% Compliance With 6 Monthly Doses of Ibandronate in Part B | | The ITT population included all participants who received at least one dose of study medication. | Posted | | Number | | percentage of participants | | Up to Month 6 | | | | ID | Title | Description |
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| OG000 | Ibandronate | Participants completed Candidate Identification Questionnaire (CIQ) in Part A and received Ibandronate 150 milligram (mg) tablet orally once-monthly up to 6 months in Part B of the study. |
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| Secondary | Percentage of Participants Who Choose a Monthly Reminder to Take Ibandronate in Part B | | The ITT population included all participants who received at least one dose of study medication. | Posted | | Number | | percentage of participants | | Visit 0 (<= Day -30) | | | | ID | Title | Description |
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| OG000 | Ibandronate | Participants completed Candidate Identification Questionnaire (CIQ) in Part A and received Ibandronate 150 milligram (mg) tablet orally once-monthly up to 6 months in Part B of the study. |
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| Secondary | Percentage of Participants Who Reported an Improvement in the Frequency of Gastro-intestinal (GI) Symptoms Per Month in Part B | | Analysis was not performed because the data were difficult or impossible to derive from the database. | Posted | | | | | | Baseline to Month 6 | | | | ID | Title | Description |
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| OG000 | Ibandronate | Participants completed Candidate Identification Questionnaire (CIQ) in Part A and received Ibandronate 150 milligram (mg) tablet orally once-monthly up to 6 months in Part B of the study. |
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| Secondary | Percentage of Participants by Age and Activity Level Reporting High Satisfaction According to the Osteoporosis Patient Satisfaction Questionnaire (OPSAT-Q) in Part B | | Analysis was not performed because the data were difficult or impossible to derive from the database. | Posted | | | | | | Month 6 | | | | ID | Title | Description |
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| OG000 | Ibandronate | Participants completed Candidate Identification Questionnaire (CIQ) in Part A and received Ibandronate 150 milligram (mg) tablet orally once-monthly up to 6 months in Part B of the study. |
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| Secondary | Osteoporosis Patient Satisfaction Questionnaire (OPSAT-Q) Domain Scores in Part B | The OPSAT-Q is a validated questionnaire designed to capture satisfaction with bisphosphonate treatment. It comprises four domains: convenience (questions 1-6), quality of life (questions 7 and 8), overall satisfaction (questions 9 and 10), and side effects (questions 11-16). Each domain (scale) ranges 0-100 scale. All items were scored such that higher scores represented greater satisfaction or less bother. Treatment satisfaction was measured with the OPSAT-Q composite satisfaction score (OPSAT-Q CSS), which was the average of the scores from the four domains of the OPSAT-Q converted to a 0-100-point scale, in which higher scores indicate greater satisfaction. | The ITT population included all participants who received at least one dose of study medication. | Posted | | Mean | Standard Deviation | units on a scale | | Baseline, Month 6 | | | | ID | Title | Description |
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| OG000 | Ibandronate | Participants completed Candidate Identification Questionnaire (CIQ) in Part A and received Ibandronate 150 milligram (mg) tablet orally once-monthly up to 6 months in Part B of the study. |
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