Clinical Evaluation of Fortilink® TETRAfuse® Interbody Fusion Device in Subjects With Degenerative Disc Disease
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.
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
- Enrollment
- 15 participants
Conditions and interventions
Conditions
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 12, 2019
- Primary completion
- Jun 29, 2023
- Completion
- Dec 29, 2023
- Last update posted
- Mar 14, 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 14, 2024 · Synced Sep 7, 2026
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Open the official record
The complete protocol, eligibility criteria, and contact information for NCT03761563 live on ClinicalTrials.gov.