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NCT04207606 · ClinicalTrials.gov registry record
Post Epidural Steroid Injection Follow-up
A clinical trial of Lumbar Spinal Stenosis and Lumbar Disc Herniation, sponsored by Vanderbilt University Medical Center.
- Completed
- Registry status
- 100
- Enrollment target
- 1
- Study location
NCT04207606 is a study of Lumbar Spinal Stenosis and Lumbar Disc Herniation that has completed, run by Vanderbilt University Medical Center. The registered enrollment target is 100 participants, below the 664-participant average among 18 other Lumbar Spinal Stenosis trials with a reported enrollment target (85% lower). The trial reports 1 study location across 1 state.
The verdict
NCT04207606, a study of Lumbar Spinal Stenosis and Lumbar Disc Herniation, has completed, sponsored by Vanderbilt University Medical Center.
- COMPLETED
- Registry status
- 100 participants
- Enrollment target
- 1
- Study location
Study Summary
To determine the expected pain response timeline for patients receiving epidural steroid injections, our team plans to assess patient pain severity and degree of pain relief every 3 days for 23 days.
Conditions Studied
Interventions
- BEHAVIORAL Post Epidural Steroid Injection Follow-up
Study Locations (1)
Tennessee
- Stallworth Rehabilitation Hospital - Nashville
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 100 participants |
| Start Date | 2020-01-03 |
| Est. Completion | 2020-12-01 |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT04207606
The ClinicalTrials.gov registry entry for NCT04207606 describes a study currently listed as completed, categorized as an unspecified phase. The registered enrollment target is 100 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 664-participant average among 18 other Lumbar Spinal Stenosis trials with a reported enrollment target (85% lower). The listed sponsor is Vanderbilt University Medical Center, which has 677 total studies on file at ClinicalTrials.gov.
The record links to 3 conditions, with Lumbar Spinal Stenosis appearing as the primary indexed condition, and to 1 intervention - of which Post Epidural Steroid Injection Follow-up is the first listed.
NCT04207606 reports 1 study location spanning 1 distinct geographic area - top geographies include Tennessee.
Frequently Asked Questions
What is clinical trial NCT04207606 about?
NCT04207606 is a clinical study titled "Post Epidural Steroid Injection Follow-up". To determine the expected pain response timeline for patients receiving epidural steroid injections, our team plans to assess patient pain severity and degree of pain relief every 3 days for 23 days.
What is the current status of trial NCT04207606?
This trial is currently completed. The enrollment target is 100 participants. The study started on 2020-01-03. Estimated completion is 2020-12-01.
What conditions does trial NCT04207606 study?
This clinical trial studies the following conditions: Lumbar Spinal Stenosis, Lumbar Disc Herniation, Lumbago.
What interventions are being tested in trial NCT04207606?
The interventions under investigation include: Post Epidural Steroid Injection Follow-up (BEHAVIORAL).
Who is sponsoring clinical trial NCT04207606?
This trial is sponsored by Vanderbilt University Medical Center, which has 677 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT04207606 being conducted?
This trial has 1 study location across Tennessee. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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