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NCT03761563 · ClinicalTrials.gov registry record

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

A clinical trial, sponsored by Xtant Medical.

Completed
Registry status
15
Enrollment target

NCT03761563: Completed study, sponsored by Xtant Medical.

NCT03761563 is a clinical trial that has completed, run by Xtant Medical. The registered enrollment target is 15 participants. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT03761563 has completed, sponsored by Xtant Medical.

COMPLETED
Registry status
15 participants
Enrollment target

Study Summary

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.

Interventions

  • DEVICE Fortilink IBF System with TETRAfuse Technology

Trial Details

FieldValue
Enrollment Target 15 participants
Start Date 2019-02-13
Est. Completion 2023-12-30
Xtant Medical

3 total trials

What the finished NCT03761563 record still lists

NCT03761563 is an observational study that tracks outcomes without assigning an intervention. The registry caps enrollment at 15 participants, a relatively small participant target.

The record links to 0 conditions, and to 1 intervention - of which Fortilink IBF System with TETRAfuse Technology is the first listed.

NCT03761563 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT03761563 about?

NCT03761563 is a clinical study titled "Clinical Evaluation of Fortilink® TETRAfuse® Interbody Fusion Device in Subjects With Degenerative Disc Disease". 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.

What is the current status of trial NCT03761563?

This trial is currently completed. The enrollment target is 15 participants. The study started on 2019-02-13. Estimated completion is 2023-12-30.

What interventions are being tested in trial NCT03761563?

The interventions under investigation include: Fortilink IBF System with TETRAfuse Technology (DEVICE).

Who is sponsoring clinical trial NCT03761563?

This trial is sponsored by Xtant Medical, which has 3 total clinical trials registered on ClinicalTrials.gov.

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Source: ClinicalTrials.gov NCT03761563, the US trial registry maintained by the National Library of Medicine. NCT03761563 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.