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NCT01053572 · ClinicalTrials.gov registry record · NA
Role of Steroids and 10% Hypertonic Sodium Chloride in Adhesiolysis in Post Lumbar Surgery Syndrome Patients
A NA study, sponsored by Pain Management Center of Paducah.
- Completed
- Registry status
- NA
- Development phase
- 240
- Enrollment target
NCT01053572 is a NA study that has completed, run by Pain Management Center of Paducah. The registered enrollment target is 240 participants.
The verdict
NCT01053572, a NA study, has completed, sponsored by Pain Management Center of Paducah.
- COMPLETED
- Registry status
- NA
- Development phase
- 240 participants
- Enrollment target
Study Summary
To evaluate the effectiveness of steroids and/or 10% hypertonic sodium chloride in percutaneous adhesiolysis in managing chronic low back and/or lower extremity pain in patients with post lumbar surgery syndrome. To evaluate and compare the adverse event profile in all groups.
Interventions
- PROCEDURE Adhesiolysis
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 240 participants |
| Start Date | 2010-02 |
| Est. Completion | 2014-01 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT01053572
The ClinicalTrials.gov registry entry for NCT01053572 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 240 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 1 intervention - of which Adhesiolysis is the first listed.
NCT01053572 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT01053572 about?
NCT01053572 is a clinical study titled "Role of Steroids and 10% Hypertonic Sodium Chloride in Adhesiolysis in Post Lumbar Surgery Syndrome Patients". To evaluate the effectiveness of steroids and/or 10% hypertonic sodium chloride in percutaneous adhesiolysis in managing chronic low back and/or lower extremity pain in patients with post lumbar surgery syndrome. To evaluate and compare the adverse event profile in all groups.
What is the current status of trial NCT01053572?
This trial is currently completed. It is a NA study. The enrollment target is 240 participants. The study started on 2010-02. Estimated completion is 2014-01.
What interventions are being tested in trial NCT01053572?
The interventions under investigation include: Adhesiolysis (PROCEDURE).
Who is sponsoring clinical trial NCT01053572?
This trial is sponsored by Pain Management Center of Paducah, which has 11 total clinical trials registered on ClinicalTrials.gov.
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