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NCT01053273 · ClinicalTrials.gov registry record · NA
A Randomized, Equivalence Trial of Percutaneous Lumbar Adhesiolysis and Caudal Epidural Steroid Injections
A NA study, sponsored by Pain Management Center of Paducah.
- Completed
- Registry status
- NA
- Development phase
- 120
- Enrollment target
NCT01053273: Completed NA study, sponsored by Pain Management Center of Paducah.
NCT01053273 is a NA study that has completed, run by Pain Management Center of Paducah. The registered enrollment target is 120 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (91% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT01053273, a NA study, has completed, sponsored by Pain Management Center of Paducah.
- COMPLETED
- Registry status
- NA
- Development phase
- 120 participants
- Enrollment target
Study Summary
The purpose of this study is to: * evaluate the effectiveness of percutaneous epidural adhesiolysis in managing chronic low back and/or lower extremity pain in patients without post lumbar surgery syndrome or spinal stenosis and compare with fluoroscopically directed caudal epidural steroid injections. * evaluate and compare the adverse event profile in all groups.
Primary Outcome
duration of significant pain relief, opioid intake, and return to work
Interventions
- PROCEDURE Caudal Epidural Injection
- PROCEDURE percutaneous adhesiolysis
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 120 participants |
| Start Date | 2010-02 |
| Est. Completion | 2014-01-27 |
| Phase | NA |
What the finished NCT01053273 record still lists
NCT01053273 is an interventional study that assigns participants to a tested intervention. The registered 120 participants enrollment target is mid-sized for trials with a published cap, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (91% lower).
The record links to 0 conditions, and to 2 interventions - of which Caudal Epidural Injection is the first listed.
NCT01053273 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT01053273 about?
NCT01053273 is a clinical study titled "A Randomized, Equivalence Trial of Percutaneous Lumbar Adhesiolysis and Caudal Epidural Steroid Injections". The purpose of this study is to: * evaluate the effectiveness of percutaneous epidural adhesiolysis in managing chronic low back and/or lower extremity pain in patients without post lumbar surgery syndrome or spinal stenosis and compare with fluoroscopically directed caudal epidural steroid injecti...
What is the current status of trial NCT01053273?
This trial is currently completed. It is a NA study. The enrollment target is 120 participants. The study started on 2010-02. Estimated completion is 2014-01-27.
What interventions are being tested in trial NCT01053273?
The interventions under investigation include: Caudal Epidural Injection (PROCEDURE), percutaneous adhesiolysis (PROCEDURE).
Who is sponsoring clinical trial NCT01053273?
This trial is sponsored by Pain Management Center of Paducah, which has 11 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT01053273's enrollment target sits among peer trials
120 762nd of 2000 higher than 1,198 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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