Effects and Safety of Epidural PDRN vs. Placebo
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- STATUS
- Recruiting
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- participants needed
- 45
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- sponsor
- Seoul National University Hospital
Summary
This is a single-center, randomized, double-blind clinical study to assess the clinical application and outcomes with epidural PDRN versus Normal saline injection in patients with spinal stenosis.
Description
Patients who are already planning to receive an Transforaminal epidural block from their clinician will be approached by study members on the day of their injection. If enrolled, the patients will be contacted every 2 weeks for 4 weeks to determine the severity of pain and degree of pain relief from the injection.
Details
| Condition | Spinal Stenosis Lumbar |
|---|---|
| Age | 19-80 years |
| Treatment | Normal saline, Polydeoxyribonucleotides |
| Clinical Study Identifier | NCT04401735 |
| Sponsor | Seoul National University Hospital |
| Last Modified on | 19 February 2024 |
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Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.
Learn moreIf you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.
Learn moreComplete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.
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