Status:
WITHDRAWN
A Study of Epidural Bupivacain-soaked Absorbable Gelatin Sponge on Post-operative Pain in Lumbar Laminectomy
Lead Sponsor:
The Cleveland Clinic
Conditions:
Lumbar Laminectomy
Eligibility:
All Genders
18-80 years
Phase:
NA
Brief Summary
The effective relief of pain is of paramount importance to anyone treating patients undergoing surgery. Post-operative pain increases the possibility of post-surgical complications, raises the cost of...
Eligibility Criteria
Inclusion
- ASA grade I or III
- scheduled to undergo lumbar laminectomy
Exclusion
- Patients who are younger than 18 years of age
- pregnant
- spinal or lateral stenosis
- previous intervertebral disc surgery at that level
- patients with history of chronicity (symptoms \>6 months duration) or coexisting medical conditions such as substance abuse or withdrawal, hyperthyroidism, anxiety disorder, affective disorder, hepatic or renal impairments
Key Trial Info
Start Date :
April 1 2013
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
February 12 2015
Estimated Enrollment :
Patients enrolled
Trial Details
Trial ID
NCT01847339
Start Date
April 1 2013
End Date
February 12 2015
Last Update
January 9 2018
Active Locations (1)
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1
Cleveland Clinic
Cleveland, Ohio, United States, 44195