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Active, not recruiting Not applicable Interventional

A Study of Infuse® Bone Graft With Mastergraft® Strip and Posterior Fixation for Posterolateral Fusion (PLF) Treatment of Multi-Level Degenerative Lumbosacral Spinal Conditions

ClinicalTrials.gov ID: NCT03118505

Public ClinicalTrials.gov record NCT03118505. 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.

ClinicalTrials.gov public records Last synced Sep 2, 2026, 1:54 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Prospective, Randomized, Multi-Center, Open-Label Pilot Study of Infuse® Bone Graft With Mastergraft® Strip and Posterior Fixation for Posterolateral Fusion (PLF) Treatment of Multi-Level Degenerative Lumbosacral Spinal Conditions

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The purpose of this study is to obtain safety and effectiveness data on the investigational device for multi-level PLF procedures and determine the most appropriate rhBMP-2 dose for use in this indication. The study information may be used for a potential pivotal study design.

Study identification

NCT ID
NCT03118505
Recruitment status
Active, not recruiting
Study type
Interventional
Phase
Not applicable
Lead sponsor
Medtronic Spinal and Biologics
Industry
Enrollment
100 participants

Conditions and interventions

Eligibility (public fields only)

Age range
21 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Jun 28, 2017
Primary completion
Jun 30, 2025
Completion
Nov 30, 2026
Last update posted
Jun 24, 2026

2017 – 2026

United States locations

U.S. sites
17
U.S. states
11
U.S. cities
16
Facility City State ZIP Site status
University of California, Davis Sacramento California 95816
Spine Colorado Durango Colorado 81301
The Steadman Clinic Vail Colorado 81657
The Spine Health Institute Altamonte Springs Florida 32701
Foundation for Orthopedic Research and Education Tampa Florida 33637
Emory University Atlanta Georgia 30329
Indiana Spine Group Carmel Indiana 46032
Fort Wayne Orthopedics Fort Wayne Indiana 46804
The University of Kansas (KUMC) Kansas City Kansas 66160
Bronson Methodist Hospital Kalamazoo Michigan 49007
Upstate Orthopedics East Syracuse New York 13057
New York-Presbyterian Hospital/Columbia University New York New York 10034
The Ohio State University Wexner Medical Center Columbus Ohio 43210
Seton Spine & Scoliosis Center Austin Texas 78731
American Neurospine Institute PLLC Plano Texas 75075
University of Virginia Health System Charlottesville Virginia 22903
University of Virginia Charlottesville Virginia 22903

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 NCT03118505, 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 Jun 24, 2026 · Synced Sep 2, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT03118505 live on ClinicalTrials.gov.

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