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| Sponsored by: |
Assistance Publique - Hôpitaux de Paris |
| Information provided by: | Assistance Publique - Hôpitaux de Paris |
| ClinicalTrials.gov Identifier: | NCT00385086 |
Purpose
TNF-alpha is the main cytokine implicated in the formation of lumbar spinal fibrosis. Inhibiting TNF-alpha could significantly decrease spinal fibrosis after lumbar discectomy.
| Condition | Intervention | Phase |
|
Post Operative Sciatica by Lumbar Spinal Fibrosis |
Drug: TNF blocker |
Phase III |
| MedlinePlus related topics: | Sciatica |
| Drug Information available for: | Tumor Necrosis Factors |
| Study Type: | Interventional |
| Study Design: | Treatment, Randomized, Double-Blind, Placebo Control, Parallel Assignment, Efficacy Study |
| Official Title: | Efficacy of TNF-Alpha Inhibition in Sciatica With Post-Operative Lumbar Spinal Fibrosis |
| Estimated Enrollment: | 40 |
| Study Start Date: | February 2007 |
| Estimated Study Completion Date: | November 2008 |
OBJECT:
Failed back surgery syndrome is still a challenging therapeutic problem. Clinical studies have demonstrated a significant association between lumbar spinal fibrosis after lumbar discectomy and the recurrence of radicular pain in 25% of cases. Forceful epidural infiltrations, radiotherapy, therapy with D-penicillamine or surgical procedures have had unfavourable results in terms of pain and cost. Magnetic resonance imaging reveals lumbar spinal fibrosis by a hyposignal in the T1 sequence and a hypersignal in T2 sequence around the spinal tissue. Tumor necrosis factor a (TNF-a) is the main cytokine implicated in the formation of tissue fibrosis. In animal models of fibrosis, TNF-a inhibition has been shown to prevent and treat tissue fibrosis.
HYPOTHESIS:
Inhibiting TNF-a could significantly decrease sciatica pain because of lumbar spinal fibrosis after lumbar discectomy by decreasing spinal fibrosis.
METHODS:
We propose a 2-year pilot prospective, randomized, double-blind, controlled study of TNF-a inhibitor (infliximab) in patients with sciatica as a result of postoperative lumbar spinal fibrosis. The infliximab group will receive one intravenous injection of 3 mg/kg infliximab. The control group will receive one physiological serum injection. Patients will be evaluated at day 0, 10, 30, 90, and 180. The main evaluation criterion will be sciatica pain as measured on a visual analog scale, with the objective of a 50% decrease in pain at day 10. This objective leads to a size of 20 patients per group. The other evaluation criteria will be clinical, functional, social, and professional. Patients will be recruited from the rehabilitation unit at Cochin teaching hospital.
Eligibility
| Ages Eligible for Study: | 18 Years and older |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria:
Exclusion Criteria:
Contacts and Locations| Contact: Francois Rannou, MD, PhD | +33158412535 | francois.rannou@cch.aphp.fr |
| Contact: Raphael Serreau, MD | +33158411180 | raphael.serreau@cch.aphp.fr |
| France | |||||
| Hopital Cochin | Recruiting | ||||
| Paris, France, 75014 | |||||
| Sub-Investigator: Serge Poiraudeau, MD, PhD | |||||
| Sub-Investigator: Michel Revel, MD | |||||
| Assistance Publique - Hôpitaux de Paris |
| Principal Investigator: | Francois Rannou, MD, PhD | AP-HP |
More Information
| Study ID Numbers: | P050312 |
| First Received: | October 4, 2006 |
| Last Updated: | April 30, 2007 |
| ClinicalTrials.gov Identifier: | NCT00385086 |
| Health Authority: | France: Afssaps - French Health Products Safety Agency |
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