Phase
Condition
Peripheral Neuropathy
Lower Back Pain
Ankylosing Spondylitis
Treatment
normal saline
Bupivacaine-Epinephrine 0.25%-1:200,000 Injectable Solution plus clonidine
Clinical Study ID
Ages 18-80 All Genders
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
Age 18-80
Undergoing one of 3 procedure types: 1) 2 or more levels of MIS decompression (e.g.,discectomy, foraminotomy, laminectomy); 2) 1-3 levels of MIS transforaminal lumbarinterbody fusion (TLIF) (with or without additional levels of MIS decompression forno greater than 3 total operative levels); 3) 1-3 levels of anterior lumbarinterbody fusion (ALIF) or MIS lateral lumbar interbody fusion (LLIF) accompanied byposterior percutaneous instrumentation at the same levels
Willing and able to give consent
Exclusion
Exclusion Criteria:
Opioid tolerant at the time of the surgical procedure--defined as consuming greaterthan 30mg of morphine milligram equivalents (MME) daily (https://www.cdc.gov/drugoverdose/prescribing/guideline.html)
Presence of an indwelling pain device (e.g., intrathecal opioid pump, spinal cordstimulator, dorsal root ganglion stimulator)
Known allergy to bupivacaine, clonidine or similar local anesthetics
Indication for surgery other than degenerative disease (e.g., neoplasm, infection,trauma)
Chronic kidney disease (stage 3 or greater), or hepatic failure
Active pregnancy
Disease process or mental illness that would preclude accurate evaluation of pain inthe perioperative period
Active Worker's Compensation litigation
Study Design
Study Description
Connect with a study center
Rush University Medical Center
Chicago, Illinois 60612
United StatesActive - Recruiting

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