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NCT05614284 · ClinicalTrials.gov registry record · NA
Comparative Analysis of Virtuos and Autograft in Lumbar Fusion
A NA study, sponsored by Orthofix.
- Terminated
- Registry status
- NA
- Development phase
- 6
- Enrollment target
NCT05614284 is a NA study that was terminated before completion, run by Orthofix. The registered enrollment target is 6 participants.
The verdict
NCT05614284, a NA study, was terminated before completion, sponsored by Orthofix.
- TERMINATED
- Registry status
- NA
- Development phase
- 6 participants
- Enrollment target
Study Summary
Compare the lumbar fusion rates at 12 and 24 months when lumbar arthrodesis is performed using Virtuos or Autograft Bone Graft. Surgical approach is limited to TLIF (MIS or Open) with posterior fixation and supplemental posterolateral fusion as directed by physician, but must comply with FDA approved/cleared indication for use and labeling.
Interventions
- DEVICE Virtuos
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 6 participants |
| Start Date | 2022-11-14 |
| Est. Completion | 2024-05-16 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT05614284
The ClinicalTrials.gov registry entry for NCT05614284 describes a study currently listed as terminated, categorized as NA. The registered enrollment target is 6 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Orthofix, which has 14 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 1 intervention - of which Virtuos is the first listed.
NCT05614284 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT05614284 about?
NCT05614284 is a clinical study titled "Comparative Analysis of Virtuos and Autograft in Lumbar Fusion". Compare the lumbar fusion rates at 12 and 24 months when lumbar arthrodesis is performed using Virtuos or Autograft Bone Graft. Surgical approach is limited to TLIF (MIS or Open) with posterior fixation and supplemental posterolateral fusion as directed by physician, but must comply with FDA approve...
What is the current status of trial NCT05614284?
This trial is currently terminated. It is a NA study. The enrollment target is 6 participants. The study started on 2022-11-14. Estimated completion is 2024-05-16.
What interventions are being tested in trial NCT05614284?
The interventions under investigation include: Virtuos (DEVICE).
Who is sponsoring clinical trial NCT05614284?
This trial is sponsored by Orthofix, which has 14 total clinical trials registered on ClinicalTrials.gov.
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