OsteoporosisBONPMSNCT01381393
BONVIVA(Ibandronate) PMS(Post-marketing Surveillance )
An observational study of Osteoporosis, run by GlaxoSmithKline at 1 site in South Korea.
Trial summary
This is an open label, multi-centre, non-interventional post-marketing surveillance. Read more about this study
- Who is it for?
- Any age, women only
- Conditions the study is for
- Osteoporosis
- What is being tested?
- Ibandronate
- How many people
- 659 participants
- Where
- 1 siteSouth Korea
- Study dates
- Jun 2007to Mar 2012
- Phase
- Observational
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages Any age
- Women only
- No healthy volunteers
- Child, Adult, Older adult
Study population: Patients administrated ibandronate with postmenopausal osteoporosis in Korea
Who may be able to join
- All subjects must satisfy the following criteria at study entry:
- Subjects diagnosed with osteoporosis in postmenopausal women.
- Subjects who the investigator believes that they can and will comply with the requirements of the protocol
- Subjects with no experience of treatment using ibandronate.
- Subjects who are administered of ibandronate in normal prescription use
Who cannot join
- Considering the nature of this non-interventional PMS study, there is no strict exclusion criteria set up. The doctors participating this study to enrol the subjects prescribed with ibandronate following the locally approved Prescribing Information.
- The following criteria should be checked at the time of study entry.
- According to contraindication on the prescribing information, ibandronate should not be administered to the following patients:
- Patients with known hypersensitivity to ibandronate or to any of its excipients
- Uncorrected hypocalcemia
- Inability to stand or sit upright for at least 60 minutes
Trial locations and contacts
1 site in 1 country.
About this study
Official title: An Open Label, Multi-centre, Non-interventional Post-marketing Surveillance to Monitor the Safety of BONVIVA(Ibandronate) Administered in Korean Patients According to the Prescribing Information
This is an open label, multi-centre, non-interventional post-marketing surveillance.
Read the detailed description
This is an open label, multi-centre, non-interventional post-marketing surveillance to monitor the safety of ibandronate administered in Korean patients according to the prescribing information.
- Conditions
- Osteoporosis
- Being tested
- Ibandronate
- Keywords
- osteoporosis, ibandronate
- Medical subject headings
- Osteoporosis
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
IbandronateDrug
Also called BONVIVA
Basically there is no treatment allocation. Subjects who would be administered of ibandronate at their physicians' discretion will be enrolled. Dosage regimen will be recommended according to the prescribing information. Subjects will be enrolled consecutively.
| Study group | Role | What they receive |
|---|---|---|
| Ibandronate | The subjects with osteoporosis in postmenopausal women Receives: Drug: Ibandronate |
What is being measured
The primary outcome is the main question the study is designed to answer.
The number of adverse event after ibandronate administration
Measured: 6 months
Secondary outcomes (2)
The number of unexpected adverse events after ibandronate administration
Measured: 6 months
The number of serious adverse events after ibandronate administration
Measured: 6 months
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted27 Jun 2011 (estimated)
- Study startJun 2007
- Primary completionMar 2012
- Study completionMar 2012
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for OsteoporosisStudies of the same condition, open and under way.
- More trials run by GlaxoSmithKlineThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Observational
- Observational model
- Cohort
- Time perspective
- Prospective
- Enrolment
- 659 participants (actual)
Sponsor and investigators
- Lead sponsor
- GlaxoSmithKline
- Sponsor type
- Industry (pharma, biotech, devices)
- Responsible party
- Sponsor
- Investigators
- GSK Clinical Trials, Study director, GlaxoSmithKline
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT01381393
- Sponsor's protocol ID
- 110603
- Acronym
- BONPMS
- Status last verified
- Nov 2012
- First submitted
- 23 Jun 2011
- Last updated
- 30 Nov 2012
- Results posted
- No
- Data monitoring committee
- No
Study at a glance
From the registry record, last updated by the sponsor on 30 Nov 2012. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- An Open Label, Multi-centre, Non-interventional Post-marketing Surveillance to Monitor the Safety of BONVIVA(Ibandronate) Administered in Korean Patients According to the Prescribing Information
- ClinicalTrials.gov ID
- NCT01381393
- Acronym / sponsor ID
- BONPMS / 110603
- Conditions
- Osteoporosis
- Keywords
- osteoporosis, ibandronate
- Study type
- Observational
- Recruitment status
- Completed
- Enrolment
- 659 participants (actual)
- Lead sponsor
- GlaxoSmithKlineIndustry (pharma, biotech, devices)
- Study start
- Jun 2007
- Primary completion
- Mar 2012 (actual)
- Study completion
- Mar 2012 (actual)
- First posted
- 27 Jun 2011 (estimated)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
This is an open label, multi-centre, non-interventional post-marketing surveillance.
Detailed description
This is an open label, multi-centre, non-interventional post-marketing surveillance to monitor the safety of ibandronate administered in Korean patients according to the prescribing information.
Study design
- Observational model
- Cohort
- Time perspective
- Prospective
- Number of arms
- 1
| Arm | Type | Receives |
|---|---|---|
| Ibandronate | – | Drug: IbandronateThe subjects with osteoporosis in postmenopausal women |
Who may qualify
- Sex
- Female only
- Healthy volunteers
- Not accepted
- Age groups
- Child, Adult, Older adult
- Study population
- Patients administrated ibandronate with postmenopausal osteoporosis in Korea
Key inclusion criteria (5 listed)
- Subjects diagnosed with osteoporosis in postmenopausal women.
- Subjects who the investigator believes that they can and will comply with the requirements of the protocol
- Subjects with no experience of treatment using ibandronate.
- Subjects who are administered of ibandronate in normal prescription use
Key exclusion criteria (6 listed)
- Considering the nature of this non-interventional PMS study, there is no strict exclusion criteria set up. The doctors participating this study to enrol the subjects prescribed with ibandronate following the locally approved Prescribing Information.
- The following criteria should be checked at the time of study entry.
- According to contraindication on the prescribing information, ibandronate should not be administered to the following patients:
- Patients with known hypersensitivity to ibandronate or to any of its excipients
- Uncorrected hypocalcemia
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| IbandronateAlso: BONVIVABasically there is no treatment allocation. Subjects who would be administered of ibandronate at their physicians' discretion will be enrolled. Dosage regimen will be recommended according to the prescribing information. Subjects will be enrolled consecutively. | Drug | Ibandronate |
Primary outcome
The number of adverse event after ibandronate administration
Time frame: 6 months
2 secondary outcomes
The number of unexpected adverse events after ibandronate administration
Time frame: 6 months
The number of serious adverse events after ibandronate administration
Time frame: 6 months
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 30 Nov 2012.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
GSK Clinical Trials study director
GlaxoSmithKline
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
An observational study of Osteoporosis, run by GlaxoSmithKline at 1 site in South Korea.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 5 inclusion and 6 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: finished, as of the sponsor's last update on 30 Nov 2012. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in South Korea. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
The number of adverse event after ibandronate administration (time frame: 6 months). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 30 Nov 2012; AzTrials last refreshed its copy on 6 Nov 2026.