# A Safety and Efficacy Study for Treatment of Painful Vertebral Compression Fractures Caused by Osteoporosis

> **NCT00290862** · NA · UNKNOWN · sponsor: **Orthovita d/b/a Stryker** · enrollment: 256 (actual)

## Conditions studied

- Spinal Fractures

## Interventions

- **DEVICE:** Percutaneous Vertebral Augmentation of compression fractures

## Key facts

- **NCT ID:** NCT00290862
- **Lead sponsor:** Orthovita d/b/a Stryker
- **Sponsor class:** INDUSTRY
- **Phase:** NA
- **Study type:** INTERVENTIONAL
- **Status:** UNKNOWN
- **Start date:** 2004-09
- **Primary completion:** —
- **Final completion:** 2009-03
- **Target enrollment:** 256 (ACTUAL)
- **Last updated:** 2008-10-15


## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT00290862

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT00290862, "A Safety and Efficacy Study for Treatment of Painful Vertebral Compression Fractures Caused by Osteoporosis". Retrieved via AI Analytics 2026-07-31 from https://api.ai-analytics.org/clinical/NCT00290862. Licensed CC0.

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