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NCT01850771 · ClinicalTrials.gov registry record · NA
Regenexx™ PL-Disc Versus Steroid Epidurals for Lumbar Radiculopathy
A NA study, sponsored by Regenexx.
- Terminated
- Registry status
- NA
- Development phase
- 8
- Enrollment target
NCT01850771: Clinical Trial NA study, sponsored by Regenexx.
NCT01850771 is a NA study that was terminated before completion, run by Regenexx. The registered enrollment target is 8 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (99% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT01850771, a NA study, was terminated before completion, sponsored by Regenexx.
- TERMINATED
- Registry status
- NA
- Development phase
- 8 participants
- Enrollment target
Study Summary
The primary objective of this study is to compare the improvement in subject-reported clinical outcomes for Regenexx PL-Disc vs. steroid epidural for treatment of lumbar radiculopathy, from baseline to 3 months, with continued evaluation of efficacy and durability up to 12 months. Secondary objectives include incidence of post-operative complications, adverse events, re-injections, and surgical intervention; change in pain score and use of pain medications.
Primary Outcome
The primary endpoint for this study is the difference between treatment groups in the within patient mean change from baseline to 3 months in Oswestry Disability Index (ODI) scores.
Interventions
- PROCEDURE Regenexx PL-Disc
- PROCEDURE Steroid Epidural
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 8 participants |
| Start Date | 2013-05 |
| Est. Completion | 2016-05 |
| Phase | NA |
Why NCT01850771 stopped before completion
NCT01850771 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 8 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (99% lower).
The record links to 0 conditions, and to 2 interventions - of which Regenexx PL-Disc is the first listed.
NCT01850771 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT01850771 about?
NCT01850771 is a clinical study titled "Regenexx™ PL-Disc Versus Steroid Epidurals for Lumbar Radiculopathy". The primary objective of this study is to compare the improvement in subject-reported clinical outcomes for Regenexx PL-Disc vs. steroid epidural for treatment of lumbar radiculopathy, from baseline to 3 months, with continued evaluation of efficacy and durability up to 12 months. Secondary objecti...
What is the current status of trial NCT01850771?
This trial is currently terminated. It is a NA study. The enrollment target is 8 participants. The study started on 2013-05. Estimated completion is 2016-05.
What interventions are being tested in trial NCT01850771?
The interventions under investigation include: Regenexx PL-Disc (PROCEDURE), Steroid Epidural (PROCEDURE).
Who is sponsoring clinical trial NCT01850771?
This trial is sponsored by Regenexx, which has 13 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT01850771's enrollment target sits among peer trials
8 1976th of 2000 higher than 19 of 2,000 other NA trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other NA 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
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