A Safety and Efficacy Study for Treatment of Painful Vertebral Compression Fractures Caused by Osteoporosis
Public ClinicalTrials.gov record NCT00290862. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.
Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.
Official title
A Randomized, Controlled Clinical Study to Evaluate the Safety and Effectiveness of CORTOSS® Synthetic Cortical Bone Void Filler in Vertebral Augmentation
Study identification
- NCT ID
- NCT00290862
- Recruitment status
- Not listed
- Study type
- Interventional
- Phase
- Not applicable
- Lead sponsor
- Orthovita d/b/a Stryker
- Industry
- Enrollment
- 256 participants
Conditions and interventions
Conditions
Interventions
- Percutaneous Vertebral Augmentation of compression fractures Device
Device
Eligibility (public fields only)
- Age range
- 18 Years and older
- Sex
- All
- Healthy volunteers
- Accepts healthy volunteers
This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.
Study timeline
- Start date
- Aug 31, 2004
- Primary completion
- Not listed
- Completion
- Feb 28, 2009
- Last update posted
- Oct 14, 2008
2004 – 2009
United States locations
- U.S. sites
- 18
- U.S. states
- 13
- U.S. cities
- 17
| Facility | City | State | ZIP | Site status |
|---|---|---|---|---|
| Scottsdale Medical Center | Scottsdale | Arizona | 85251 | — |
| Core Orthopaedic Medical Center, P.C. | Encinitas | California | 92024 | — |
| Eisenhower Medical Center | Rancho Mirage | California | 92270 | — |
| St. John's Spine Institute | Santa Monica | California | 90404 | — |
| Indian River Radiology | Vero Beach | Florida | 32960 | — |
| Emory Orthopaedics and Spine Center | Atlanta | Georgia | 30329 | — |
| Millenium Pain Center | Bloomington | Illinois | 61701 | — |
| Northwestern University | Chicago | Illinois | 60611 | — |
| The Spine Institute of Louisiana | Shreveport | Louisiana | 71101 | — |
| Washington University Medical Center | St Louis | Missouri | 63110 | — |
| Hospital for Special Surgery (HSS) | New York | New York | 10021 | — |
| Montefiore Medical Center | The Bronx | New York | 10467 | — |
| Mission Hospitals | Asheville | North Carolina | 28801 | — |
| Dayton Interventional Radiology | Kettering | Ohio | 45409 | — |
| Edmond Medical Center | Oklahoma City | Oklahoma | 73034 | — |
| Mercy Health Center | Oklahoma City | Oklahoma | 73120 | — |
| Pennsylvania Hospital | Philadelphia | Pennsylvania | 19107 | — |
| Endovascular Center of Houston | Houston | Texas | 77030 | — |
Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.
About this trial record page
- What this page shows
- Public field values for ClinicalTrials.gov record NCT00290862, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
- What this page does not do
- No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
- Where the data comes from
- Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
- Last refresh
- Last update posted Oct 14, 2008 · Synced Jul 22, 2026
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Open the official record
The complete protocol, eligibility criteria, and contact information for NCT00290862 live on ClinicalTrials.gov.