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Lumbar Spinal Fibrosis and TNF Alpha Inhibition

This study is currently recruiting participants.
Verified by Assistance Publique - Hôpitaux de Paris, April 2007

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   

U.S. FDA Resources

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

Further study details as provided by Assistance Publique - Hôpitaux de Paris:

Primary Outcome Measures:
  • Sciatica pain

Secondary Outcome Measures:
  • Functional assessments

Estimated Enrollment:   40
Study Start Date:   February 2007
Estimated Study Completion Date:   November 2008

Detailed Description:

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

Criteria

Inclusion Criteria:

  • age over 18 years old
  • sciatica post discectomy
  • Pain with VAS > 40 mm and impossibility to have his usual activity
  • Surgical discectomy (less than 2 years and more than 6 months)
  • Painless of more than one month and less than one year after the discectomy
  • MRI with gadolinium injection of less than 6 months and done more than 6 months after the discectomy
  • Presence of spinal fibrosis on MRI (hyposignal in T1 enhanced by gadolinium and hypersignal in T2)
  • failure of epidural injection treatment
  • absence of tuberculosis
  • contraception for woman
  • informed consent

Exclusion Criteria:

  • Chronic psychiatric pathologies not treated
  • Presence of conflict between nerve root and herniated disc or disc fragments or spinal stenosis
  • severe cognitives troubles
  • severe cardiac failure (class III or IV)
  • Tuberculosis (active or latent), severe infections
  • Cancers
  • Allergy reactions to the drug studied
  • Difficulties to understand french
  • Patients enrolled in another clinical trial in the past three months
  • pregnancy, breastfeeding or no contraception
  Contacts and Locations

Please refer to this study by its ClinicalTrials.gov identifier: NCT00385086

Contacts
Contact: Francois Rannou, MD, PhD     +33158412535     francois.rannou@cch.aphp.fr    
Contact: Raphael Serreau, MD     +33158411180     raphael.serreau@cch.aphp.fr    

Locations
France
Hopital Cochin     Recruiting
      Paris, France, 75014
      Sub-Investigator: Serge Poiraudeau, MD, PhD            
      Sub-Investigator: Michel Revel, MD            

Sponsors and Collaborators
Assistance Publique - Hôpitaux de Paris

Investigators
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

Keywords provided by Assistance Publique - Hôpitaux de Paris:
Sciatica  
Pain  
TNF-alpha  
Discectomy
Fibrosis
Spine

Study placed in the following topic categories:
Sciatica
Signs and Symptoms
Neuromuscular Diseases
Neuralgia
Fibrosis
Peripheral Nervous System Diseases
Neurologic Manifestations
Pain
Mononeuropathies

Additional relevant MeSH terms:
Sciatic Neuropathy
Pathologic Processes
Nervous System Diseases

ClinicalTrials.gov processed this record on November 20, 2008




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