# Medtronic SCORE Study - Study of Curette Use for Obtaining Restoration of Vertebral Body Anatomy in Balloon Kyphoplasty

> **NCT00810043** · PHASE4 · COMPLETED · sponsor: **Medtronic Spine LLC** · enrollment: 120 (actual)

## Conditions studied

- Vertebral Body Compression Fractures (VCFs)

## Interventions

- **DEVICE:** Kyphon® Curette

## Key facts

- **NCT ID:** NCT00810043
- **Lead sponsor:** Medtronic Spine LLC
- **Sponsor class:** INDUSTRY
- **Phase:** PHASE4
- **Study type:** INTERVENTIONAL
- **Status:** COMPLETED
- **Start date:** 2009-02
- **Primary completion:** 2010-10
- **Final completion:** 2010-10
- **Target enrollment:** 120 (ACTUAL)
- **Last updated:** 2017-12-08


## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT00810043

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT00810043, "Medtronic SCORE Study - Study of Curette Use for Obtaining Restoration of Vertebral Body Anatomy in Balloon Kyphoplasty". Retrieved via AI Analytics 2026-05-24 from https://api.ai-analytics.org/clinical/NCT00810043. Licensed CC0.

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