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Completed No phase listed Observational

Clinical Evaluation of Fortilink® TETRAfuse® Interbody Fusion Device in Subjects With Degenerative Disc Disease

ClinicalTrials.gov ID: NCT03761563

Public ClinicalTrials.gov record NCT03761563. 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 Oct 22, 2026, 10:27 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

Clinical Evaluation of Fortilink® TETRAfuse® Interbody Fusion Device in Subjects With Degenerative Disc Disease (FORTE)

Brief summary

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

This is a prospective, multi-center, non-randomized post-market evaluation designed to collect and evaluate data on the safety and performance of the Fortilink IBF System with TETRAfuse 3D Technology.

Study identification

NCT ID
NCT03761563
Recruitment status
Completed
Study type
Observational
Phase
Not listed
Lead sponsor
Xtant Medical
Industry
Enrollment
15 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 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
Feb 13, 2019 (Actual)
Primary completion
Jun 30, 2023 (Actual)
Completion
Dec 30, 2023 (Actual)
Last update posted
Mar 15, 2024

2019 – 2023

United States locations

U.S. sites
14
U.S. states
10
U.S. cities
14
Facility City State ZIP Site status
Los Angeles Orthopedic Institute Sherman Oaks California 91403 —
Rocky Mountain Spine Clinic Lone Tree Colorado 80124 —
Florida Back Institute Boca Raton Florida 33496 —
South Florida Spine & Orthopaedics Coconut Creek Florida 33073 —
Spine Institute of South Florida Delray Beach Florida 33484 —
Indiana Spine Center Indianapolis Indiana 47905 —
Orthopaedic Institute of Western Kentucky Paducah Kentucky 42001 —
OrthoBethesda Bethesda Maryland 20817 —
ReVive Spine Center Niagara Falls New York 14304 —
The Lindner Center for Research & Education at The Christ Hospital Cincinnati Ohio 45219 —
Rothman Orthopaedic Institute Philadelphia Pennsylvania 19107 —
Allegheny General Hospital Pittsburgh Pennsylvania 15212 —
Spine MD North Richland Hills Texas 76182 —
Northwood Ortho-Spine The Woodlands Texas 77382 —

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 NCT03761563, 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 Mar 15, 2024 · Synced Oct 22, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT03761563 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →