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RECRUITING
NCT05329129

OssDsign® Spine Registry Study ("Propel")

Sponsor: OssDsign

View on ClinicalTrials.gov

Summary

The purpose of this multi-center, prospective, observational registry is to gather information on the clinical outcomes and real-world use of commercially available bone graft substitutes manufactured by OssDsign® AB, in patients who require spine fusion.

Official title: PROSPECTIVE OBSERVATIONAL SPINE FUSION REGISTRY FOR OssDsign® BONE GRAFT SUBSTITUTES IN REAL WORLD CLINICAL PRACTICE

Key Details

Gender

All

Age Range

21 Years - Any

Study Type

OBSERVATIONAL

Enrollment

450

Start Date

2022-03-23

Completion Date

2027-04-01

Last Updated

2025-12-02

Healthy Volunteers

Not specified

Interventions

DEVICE

OssDsign® Catalyst

An osteoconductive, resorbable, porous, 100 % nano synthetic calcium phosphate bone void filler

Locations (13)

Community Health Partners Neuroscience

Fresno, California, United States

San Diego Neurosurgery

San Diego, California, United States

Orthopedic Associates of Hartford

Hartford, Connecticut, United States

Central Connecticut Neurosurgery and Spine

New Britian, Connecticut, United States

Yale Center for Clinical Investigation, Yale School of Medicine

New Haven, Connecticut, United States

Minimally Invasive Spine Center of South Florida

Miami, Florida, United States

Foundation for Orthopaedic Research and Education

Tampa, Florida, United States

Northeast Georgia Medical Center

Gainesville, Georgia, United States

Carle Foundation Hospital, NeuroScience Institute

Urbana, Illinois, United States

Orthopaedic Institute of Western Kentucky

Paducah, Kentucky, United States

OrthoBethesda Research Foundation

Bethesda, Maryland, United States

Twin Cities Orthopedics

Edina, Minnesota, United States

University Orthopedics Center

State College, Pennsylvania, United States