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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 is a NA study that was terminated before completion, run by Regenexx. The registered enrollment target is 8 participants.
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.
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 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT01850771
The ClinicalTrials.gov registry entry for NCT01850771 describes a study currently listed as terminated, categorized as NA. The registered enrollment target is 8 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Regenexx, which has 13 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 2 interventions - of which Regenexx PL-Disc is the first listed.
NCT01850771 reports 0 study locations.
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.
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