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NCT00148915 · ClinicalTrials.gov registry record · Phase 4
A Study To Assess the Quality and Strength of Bone in Women Participants With Osteoporosis Taking Oral Ibandronate Versus Placebo
A Phase 4 study, sponsored by Hoffmann-La Roche.
- Completed
- Registry status
- Phase 4
- Development phase
- 98
- Enrollment target
NCT00148915: Completed Phase 4 study, sponsored by Hoffmann-La Roche.
NCT00148915 is a Phase 4 study that has completed, run by Hoffmann-La Roche. The registered enrollment target is 98 participants, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (81% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT00148915, a Phase 4 study, has completed, sponsored by Hoffmann-La Roche.
- COMPLETED
- Registry status
- Phase 4
- Development phase
- 98 participants
- Enrollment target
Study Summary
The purpose of this randomized, double-blind, placebo-controlled study is to estimate the effect of oral ibandronate sodium (Boniva) taken once monthly versus placebo on bone quality and strength at the proximal femur at one year.
Interventions
- DRUG Placebo
- DRUG ibandronate
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 98 participants |
| Start Date | 2005-08 |
| Est. Completion | 2007-08 |
| Phase | Phase 4 |
What the finished NCT00148915 record still lists
NCT00148915 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 98 participants, a relatively small participant target, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (81% lower).
The record links to 0 conditions, and to 2 interventions - of which Placebo is the first listed.
NCT00148915 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT00148915 about?
NCT00148915 is a clinical study titled "A Study To Assess the Quality and Strength of Bone in Women Participants With Osteoporosis Taking Oral Ibandronate Versus Placebo". The purpose of this randomized, double-blind, placebo-controlled study is to estimate the effect of oral ibandronate sodium (Boniva) taken once monthly versus placebo on bone quality and strength at the proximal femur at one year.
What is the current status of trial NCT00148915?
This trial is currently completed. It is a Phase 4 study. The enrollment target is 98 participants. The study started on 2005-08. Estimated completion is 2007-08.
What interventions are being tested in trial NCT00148915?
The interventions under investigation include: Placebo (DRUG), ibandronate (DRUG).
Who is sponsoring clinical trial NCT00148915?
This trial is sponsored by Hoffmann-La Roche, which has 909 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT00148915's enrollment target sits among peer trials
98 854th of 2000 higher than 1,140 of 2,000 other Phase 4 trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Phase 4 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source ClinicalTrials.gov registry export · 2026-08-08
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