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NCT03647501 · ClinicalTrials.gov registry record · NA
Lumbar Fusion With Nexxt Spine 3D-Printed Titanium Interbody Cages
A NA study, sponsored by Ohio State University.
- Completed
- Registry status
- NA
- Development phase
- 53
- Enrollment target
NCT03647501 is a NA study that has completed, run by Ohio State University. The registered enrollment target is 53 participants.
The verdict
NCT03647501, a NA study, has completed, sponsored by Ohio State University.
- COMPLETED
- Registry status
- NA
- Development phase
- 53 participants
- Enrollment target
Study Summary
The purpose of this randomized controlled trial is to assess and compare radiographic and clinical outcomes in patients who are to undergo combined interbody/posterolateral lumbar fusion procedures, supplemented with pedicle screw instrumentation, using one of the following interbody cages; the Nexxt Spine Nexxt MatrixxTM 3D-printed titanium cage or the HonourTM poly-ether-ether-ketone cage.
Interventions
- DEVICE Interbody cage (titanium)
- DEVICE Interbody cage (PEEK)
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 53 participants |
| Start Date | 2018-08-22 |
| Est. Completion | 2022-03-16 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT03647501
The ClinicalTrials.gov registry entry for NCT03647501 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 53 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Ohio State University, which has 552 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 2 interventions - of which Interbody cage (titanium) is the first listed.
NCT03647501 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT03647501 about?
NCT03647501 is a clinical study titled "Lumbar Fusion With Nexxt Spine 3D-Printed Titanium Interbody Cages". The purpose of this randomized controlled trial is to assess and compare radiographic and clinical outcomes in patients who are to undergo combined interbody/posterolateral lumbar fusion procedures, supplemented with pedicle screw instrumentation, using one of the following interbody cages; the Nexx...
What is the current status of trial NCT03647501?
This trial is currently completed. It is a NA study. The enrollment target is 53 participants. The study started on 2018-08-22. Estimated completion is 2022-03-16.
What interventions are being tested in trial NCT03647501?
The interventions under investigation include: Interbody cage (titanium) (DEVICE), Interbody cage (PEEK) (DEVICE).
Who is sponsoring clinical trial NCT03647501?
This trial is sponsored by Ohio State University, which has 552 total clinical trials registered on ClinicalTrials.gov.
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