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NCT01153425 · ClinicalTrials.gov registry record · Phase 4
µMRI of Therapeutic Intervention in Postmenopausal Osteoporosis
A Phase 4 study, sponsored by University of Pennsylvania.
- Completed
- Registry status
- Phase 4
- Development phase
- 33
- Enrollment target
NCT01153425: Completed Phase 4 study, sponsored by University of Pennsylvania.
NCT01153425 is a Phase 4 study that has completed, run by University of Pennsylvania. The registered enrollment target is 33 participants, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (94% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT01153425, a Phase 4 study, has completed, sponsored by University of Pennsylvania.
- COMPLETED
- Registry status
- Phase 4
- Development phase
- 33 participants
- Enrollment target
Study Summary
The purpose of this study is to apply a novel advanced magnetic resonance imaging methodology to evaluate the response to drug intervention involving two treatment arms of postmenopausal participants with osteoporosis, randomized into either a teriparatide (Forteo™) or zoledronic acid (Reclast™) group.
Primary Outcome
Ratio of the volume densities of surface (S) and curve (C)-type voxels, S/C
Interventions
- DRUG Zoledronic Acid
- DRUG Teriparatide
- OTHER Virtual Bone Biopsy
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 33 participants |
| Start Date | 2008-07 |
| Est. Completion | 2012-12 |
| Phase | Phase 4 |
What the finished NCT01153425 record still lists
NCT01153425 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 33 participants, a relatively small participant target, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (94% lower).
The record links to 0 conditions, and to 3 interventions - of which Zoledronic Acid is the first listed.
NCT01153425 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT01153425 about?
NCT01153425 is a clinical study titled "µMRI of Therapeutic Intervention in Postmenopausal Osteoporosis". The purpose of this study is to apply a novel advanced magnetic resonance imaging methodology to evaluate the response to drug intervention involving two treatment arms of postmenopausal participants with osteoporosis, randomized into either a teriparatide (Forteo™) or zoledronic acid (Reclast™) gro...
What is the current status of trial NCT01153425?
This trial is currently completed. It is a Phase 4 study. The enrollment target is 33 participants. The study started on 2008-07. Estimated completion is 2012-12.
What interventions are being tested in trial NCT01153425?
The interventions under investigation include: Zoledronic Acid (DRUG), Teriparatide (DRUG), Virtual Bone Biopsy (OTHER).
Who is sponsoring clinical trial NCT01153425?
This trial is sponsored by University of Pennsylvania, which has 1,423 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT01153425's enrollment target sits among peer trials
33 1528th of 2000 higher than 467 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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