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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 is a NA study that has completed, run by Pain Management Center of Paducah. The registered enrollment target is 120 participants.

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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.

Interventions

  • PROCEDURE Caudal Epidural Injection
  • PROCEDURE percutaneous adhesiolysis

Trial Details

FieldValue
Enrollment Target 120 participants
Start Date 2010-02
Est. Completion 2014-01-27
Phase NA

Sponsor

Pain Management Center of Paducah

11 total trials

What the Registry Record Tells You About NCT01053273

The ClinicalTrials.gov registry entry for NCT01053273 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 120 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Pain Management Center of Paducah, which has 11 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 2 interventions - of which Caudal Epidural Injection is the first listed.

NCT01053273 reports 0 study locations.

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.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.