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Randomized Controlled Trial
Oxiplex reduces leg pain, back pain, and associated symptoms after lumbar discectomy.
- Alfred L Rhyne, Scott L Blumenthal, Edmund H Frank, Ken Y Hsu, Kee D Kim, Jim A Youssef, Jeffrey C Wang, Paul Arnold, Mohammed BenDebba, Kathleen M Block, Thomas G Juarez, Richard P Chiacchierini, Ronald J Ehmsen, John S Krelle, Gere S diZerega, and Oxiplex Clinical Study Group.
- OrthoCarolina Spine Center, Charlotte, NC, USA.
- Spine. 2012 Apr 15;37(8):631-41.
Study DesignProspective, randomized, blinded clinical trial.ObjectiveTo evaluate effectiveness of Oxiplex gel for reduction of pain and associated symptoms after lumbar discectomy.Summary Of Background DataOxiplex gel (carboxymethylcellulose, polyethylene oxide, and calcium) is used during discectomy to coat the surgical site for reduction of pain and symptoms after lumbar discectomy.MethodsPatients undergoing single-level lumbar discectomy performed by laminectomy or laminotomy and randomized to receive either surgery plus Oxiplex gel (treatment group) or surgery alone (control group) were assessed 6 months after surgery using (1) a quality of life questionnaire (Lumbar Spine Outcomes Questionnaire [LSOQ]) and (2) clinical evaluations.ResultsThere were no statistically significant differences in baseline demographics, surgical procedures, LSOQ scores, and clinical evaluations between treatment (N = 177) and control (N = 175) groups. More gel-treated patients were satisfied with outcome of their surgical treatment than control patients (P = 0.05). The gel-treated group showed greater reductions in pain and symptoms from baseline compared with surgery-only controls. Additional benefits of gel were consistently shown in reduction of leg and back pain at 6 months in the patient population having substantial back pain at baseline (greater than or equal to the median LSOQ pain score of 63). In that population, there was a statistically significant reduction of leg pain and back pain (P < 0.01) in the treatment group compared with controls. Fewer patients in the treatment group had abnormal musculoskeletal physical examinations at 6 months compared with controls. There were no cases of cerebrospinal fluid leaks and no differences in laboratory values or vital signs. Patients in the treatment group had less hypoesthesia, paraesthesia, sensory loss, and fewer reoperations during the 6-month follow-up than controls (1 vs. 6).ConclusionThese data demonstrate improvements in clinical outcomes resulting from the use of Oxiplex gel in discectomy procedures for treatment of lumbar disc herniation.
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