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NCT01406405 · ClinicalTrials.gov registry record
PEEK and Allograft Spacers Evaluation in Spinal Fusion Surgeries
A clinical trial of Degenerative Disc Disease, sponsored by Justin Parker Neurological Institute.
- Completed
- Registry status
- 240
- Enrollment target
- 1
- Study location
NCT01406405: Completed study of Degenerative Disc Disease, sponsored by Justin Parker Neurological Institute.
NCT01406405 is a study of Degenerative Disc Disease that has completed, run by Justin Parker Neurological Institute. The registered enrollment target is 240 participants, above the 163-participant average among 42 other Degenerative Disc Disease trials with a reported enrollment target (47% higher). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT01406405, a study of Degenerative Disc Disease, has completed, sponsored by Justin Parker Neurological Institute.
- COMPLETED
- Registry status
- 240 participants
- Enrollment target
- 1
- Study location
Study Summary
Purpose The primary purpose of this study is to prospectively compare clinical and radiographic clinical outcomes in patients undergoing cervical or lumbar interbody fusions and randomized to receive either polyetheretherketone (PEEK) or cortical allografts.
Primary Outcome
Improvement in the Neck/Arm or Low Back/Leg Visual Analog pain Scale (VAS) scores. A 30% reduction in pain intensity will be considered to be a successful response to treatment.
Conditions Studied
Interventions
- PROCEDURE Posterior/Transforaminal Lumbar Interbody Fusion (P/TLIF), Anterior Cervical Discectomy and Fusion (ACDF)
Study Locations (1)
Colorado
- Boulder Neurosurgical Associates - Boulder
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 240 participants |
| Start Date | 2011-07 |
| Est. Completion | 2018-05-16 |
What the finished NCT01406405 record still lists
NCT01406405 is an observational study that tracks outcomes without assigning an intervention. The registered 240 participants enrollment target is mid-sized for trials with a published cap, above the 163-participant average among 42 other Degenerative Disc Disease trials with a reported enrollment target (47% higher).
The record links to 1 condition, with Degenerative Disc Disease appearing as the primary indexed condition, and to 1 intervention - of which Posterior/Transforaminal Lumbar Interbody Fusion (P/TLIF), Anterior Cervical Discectomy and Fusion (ACDF) is the first listed.
NCT01406405 reports a single indexed study location in Colorado.
Frequently Asked Questions
What is clinical trial NCT01406405 about?
NCT01406405 is a clinical study titled "PEEK and Allograft Spacers Evaluation in Spinal Fusion Surgeries". Purpose The primary purpose of this study is to prospectively compare clinical and radiographic clinical outcomes in patients undergoing cervical or lumbar interbody fusions and randomized to receive either polyetheretherketone (PEEK) or cortical allografts.
What is the current status of trial NCT01406405?
This trial is currently completed. The enrollment target is 240 participants. The study started on 2011-07. Estimated completion is 2018-05-16.
What conditions does trial NCT01406405 study?
This clinical trial studies the following conditions: Degenerative Disc Disease.
What interventions are being tested in trial NCT01406405?
The interventions under investigation include: Posterior/Transforaminal Lumbar Interbody Fusion (P/TLIF), Anterior Cervical Discectomy and Fusion (ACDF) (PROCEDURE).
Who is sponsoring clinical trial NCT01406405?
This trial is sponsored by Justin Parker Neurological Institute, which has 4 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT01406405 being conducted?
This trial has 1 study location across Colorado. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
Learn More About Clinical Trials
Similar trials for Degenerative Disc Disease
Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.
Where NCT01406405's enrollment target sits among peer trials
240 9th of 42 higher than 34 of 42 other Degenerative Disc Disease trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Degenerative Disc Disease trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source ClinicalTrials.gov registry export · 2026-08-08
-
OssDsign® Spine Registry Study ("Propel")
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-
A Study to Evaluate the Effectiveness of IDCT (Intradiscal Cell Therapy) in Subjects With One Level, Symptomatic Mild to Moderate Lumbar Degenerative Disc Disease
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LDGraft in Single Level Anterior Lumbar Interbody Fusion (ALIF)
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Investigation of DEXA-C Anterior Cervical Interbody System
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Post Marketing Study of MagnetOs Easypack Putty Standalone Compared to Demineralized Bone Matrix or Fibers Mixed With Autograft in Patients Undergoing Posterolateral Lumbar Fusion
RECRUITING · NA
-
Trial for Treating Painful Degenerative Disc Disease
RECRUITING · NA
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