Other Clinical Trial - SpineJack System Postmarket Registry

Status Active, not recruiting

Clinical Trial Summary

This postmarket registry is intended to prospectively collect real world data to support ongoing safety and performance of the SpineJack system.

Clinical Trial Description

The SpineJack System Registry will employ a prospective, multicenter, observational, consecutive enrollment design. The sample size for this Registry will include at least 400 patients treated for VCFs across approximately 10 sites. A total of 240 patients will be treated with the SpineJack system and 160 patients will be treated with other vertebral augmentation (VA) procedures, such as BKP or VP. Sites within the U.S. may include healthcare professionals (HCPs) that are surgeons, pain physicians and/or interventional radiologists. ;

Study Design

Related Conditions & MeSH terms

Fractures, Compression
Osteoporotic Vertebral Compression Fractures

Clinical Trial Details

NCT number	NCT04795765
Study type	Observational [Patient Registry]
Source	Stryker Instruments
Contact
Status	Active, not recruiting
Phase
Start date	August 19, 2019
Completion date	December 2024

View Details

See also
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Recruiting	`NCT06270173` - Post-Market Study of The Tripod-Fix Vertebral Body Augmentation System in Osteoporotic Vertebral Compression Fractures	N/A