Clinical trial

Epidural Steroid Injection With Supplemental Oral Eplerenone for Low Back Pain: A Prospective, Double Blind Randomized Trial

Name
2017-2713
Description
Low back pain is a leading cause of disability and health care costs in the United States, and treatments are ineffective for many patients. Epidural steroid injections are a common treatment, but their efficacy has been questioned and for many patients they do not provide complete relief. The investigators hypothesize, based on preclinical studies, that lack of complete efficacy may be due to the fact that clinically used steroids activate not only the intended drug target, the glucocorticoid receptor, but also the pro-inflammatory mineralocorticoid receptor. To test this hypothesis, this pilot study will recruit patients scheduled for lumbar epidural steroid injections for degenerative disc disease, and randomize them to receive a concurrent treatment with oral eplerenone (a clinically approved antagonist of the mineralocorticoid receptor) or placebo for 10 days starting just after the epidural injection. At several time points during the following year, subjects will answer the Oswestry Low Back Pain Questionnaire, to report on both pain and functional outcomes.
Trial arms
Trial start
2023-06-01
Estimated PCD
2025-12-01
Trial end
2026-06-01
Status
Withdrawn
Phase
Early phase I
Treatment
Eplerenone 50 Mg Tab
50 mg PO per day for 10 days
Arms:
Experimental
Other names:
Inspra
Placebo Oral Tablet
PO once daily for 10 days
Arms:
Control
Other names:
placebo for eplerenone
Primary endpoint
change in Oswestry Low Back Pain Disability Questionnaire at 12 months
Difference between score prior to and 12 months after epidural steroid injection
Eligibility criteria
Inclusion Criteria: * diagnosis of lumbar degenerative disc disease demonstrated on either lumbar X-Ray or lumbar MRI. * radicular symptoms or electromyograph consistent with radiculopathy and exam findings corresponding to this diagnosis * Scheduled for lumbar epidural steroid injection at participating clinics as part of routine clinical care * Negative pregnancy test, if of childbearing potential Exclusion Criteria: * Unable to complete questionnaires or give informed consent in English * Unavailable for follow-up contacts to complete questionnaires * Renal impairment (estimated glomerular filtration rate \<50 mL/min or serum creatinine \>1.8mg/dL) on metabolic panel obtained just prior to epidural injections. * Elevated serum potassium (\>5.5 milliequivalents/L) on metabolic panel obtained just prior to epidural injections. * Have undergone previous lumbar surgery within the past year. * Treated with lumbar epidural steroid injection within the past 3 months at the time of consent. * Diabetic * Systolic blood pressure reading less than 100 mm Hg at most recent pain clinic visit. * Prescribed protease inhibitors. * Taking strong CYP3A4 inhibitors * Taking potassium supplements or potassium-sparing diuretics (amiloride, spironolactone, or triamterene) or using salt substitutes that contain potassium (examples given below and in the prescreening document to be used by the study nurse). * Lactating.
Protocol
{'studyType': 'INTERVENTIONAL', 'phases': ['PHASE4'], 'designInfo': {'allocation': 'RANDOMIZED', 'interventionModel': 'PARALLEL', 'interventionModelDescription': 'Double blind placebo controlled. Equal numbers of subjects receive 10 day course of eplerenone or placebo following their clinically indicated epidural steroid injection', 'primaryPurpose': 'TREATMENT', 'maskingInfo': {'masking': 'TRIPLE', 'maskingDescription': 'Drug or look-alike placebo dispensed according to a randomization schedule.', 'whoMasked': ['PARTICIPANT', 'CARE_PROVIDER', 'INVESTIGATOR']}}, 'enrollmentInfo': {'count': 0, 'type': 'ACTUAL'}}
Updated at
2023-03-17

1 organization

1 product

1 drug

3 indications

Product
Eplerenone
Indication
Sciatica
Indication
Low Back Pain