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NCT00370799 · ClinicalTrials.gov registry record · Early Phase 1

Effectiveness of Caudal Epidural Injections in Treatment of Chronic Low Back and Lower Extremity Pain

A Early Phase 1 study of Low Back Pain, sponsored by Pain Management Center of Paducah.

Completed
Registry status
Early Phase 1
Development phase
240
Enrollment target
1
Study location

NCT00370799 is a Early Phase 1 study of Low Back Pain that has completed, run by Pain Management Center of Paducah. The registered enrollment target is 240 participants, below the 502-participant average among 122 other Low Back Pain trials with a reported enrollment target (52% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT00370799, a Early Phase 1 study of Low Back Pain, has completed, sponsored by Pain Management Center of Paducah.

COMPLETED
Registry status
Early Phase 1
Development phase
240 participants
Enrollment target
1
Study location

Study Summary

To demonstrate clinically significant improvements or lack thereof in the caudal epidural patients with our without steroids. To evaluate differences in outcomes in patients receiving steroids compared to those patients randomized to the local anesthetic group who did not receive steroids. To assess improvements among patients and compare steroid groups with each other and local anesthetic group. To evaluate and compare the adverse event profile in all patients

Conditions Studied

Low Back Pain

Interventions

  • DRUG Caudal epidural injection
  • DRUG Caudal Epidural Injection with generic Celestone
  • DRUG Caudal Epidural Injection with Celestone
  • DRUG Caudal Epidural Injection with DepoMedrol

Study Locations (1)

Kentucky

  • Ambulatory Surgery Center - Paducah

Trial Details

FieldValue
Enrollment Target 240 participants
Start Date 2007-01
Est. Completion 2010-03
Phase Early Phase 1

Sponsor

Pain Management Center of Paducah

11 total trials

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What the Registry Record Tells You About NCT00370799

The ClinicalTrials.gov registry entry for NCT00370799 describes a study currently listed as completed, categorized as Early Phase 1. The registered enrollment target is 240 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 502-participant average among 122 other Low Back Pain trials with a reported enrollment target (52% lower). The listed sponsor is Pain Management Center of Paducah, which has 11 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Low Back Pain appearing as the primary indexed condition, and to 4 interventions - of which Caudal epidural injection is the first listed.

NCT00370799 reports 1 study location spanning 1 distinct geographic area - top geographies include Kentucky.

Frequently Asked Questions

What is clinical trial NCT00370799 about?

NCT00370799 is a clinical study titled "Effectiveness of Caudal Epidural Injections in Treatment of Chronic Low Back and Lower Extremity Pain". To demonstrate clinically significant improvements or lack thereof in the caudal epidural patients with our without steroids. To evaluate differences in outcomes in patients receiving steroids compared to those patients randomized to the local anesthetic group who did not receive steroids. To asse...

What is the current status of trial NCT00370799?

This trial is currently completed. It is a Early Phase 1 study. The enrollment target is 240 participants. The study started on 2007-01. Estimated completion is 2010-03.

What conditions does trial NCT00370799 study?

This clinical trial studies the following conditions: Low Back Pain.

What interventions are being tested in trial NCT00370799?

The interventions under investigation include: Caudal epidural injection (DRUG), Caudal Epidural Injection with generic Celestone (DRUG), Caudal Epidural Injection with Celestone (DRUG), Caudal Epidural Injection with DepoMedrol (DRUG).

Who is sponsoring clinical trial NCT00370799?

This trial is sponsored by Pain Management Center of Paducah, which has 11 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT00370799 being conducted?

This trial has 1 study location across Kentucky. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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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.