Try our beta test site
IMPORTANT: Listing of a study on this site does not reflect endorsement by the National Institutes of Health. Talk with a trusted healthcare professional before volunteering for a study. Read more...

Assessment of the Efficacy of an Intradiscal Injection of Corticoids in Modic I Discopathies. (MODISC)

This study is currently recruiting participants. (see Contacts and Locations)
Verified May 2016 by University Hospital, Montpellier
Information provided by (Responsible Party):
University Hospital, Montpellier Identifier:
First received: September 22, 2012
Last updated: May 31, 2016
Last verified: May 2016
The treatment of chronic low back pain is a major objective of public healthcare, because it causes an important number of sick leaves. A correlation between clinical observations and an inflammatory discopathy has been underlined, but there is currently any reference treatment. In this study, the main objective is to assess the efficacy of an intradiscal injection of corticoids versus local anaesthetic on the treatment of pain of patients with low back pain associated to a Modic I discopathy.

Condition Intervention Phase
Low Back Pain
Modic I Discopathy
Drug: Hydrocortancyl.
Drug: Lidocaine
Phase 3

Study Type: Interventional
Study Design: Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Single Blind (Participant)
Primary Purpose: Treatment
Official Title: Assessment of the Efficacy of an Intradiscal Injection of Corticoids in Modic I Discopathies.

Resource links provided by NLM:

Further study details as provided by University Hospital, Montpellier:

Primary Outcome Measures:
  • Pain assessment [ Time Frame: 6 months ]
    The pain will be assessed by the visual analog scale (VAS).

Secondary Outcome Measures:
  • Quality of life assessment [ Time Frame: 6 months ]
    Quality of life will be assessed by the self-questionnaire SF-36.

  • Consumption of analgesics and NSAIDs assessment [ Time Frame: 6 months ]
  • Specific low back pain parameters assessment [ Time Frame: 6 months ]
    Low back pain parameters will be assessed by the Dallas scale and the Oswestry scale.

Estimated Enrollment: 40
Study Start Date: July 2012
Estimated Study Completion Date: June 2017
Estimated Primary Completion Date: December 2016 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
Active Comparator: Corticoids
A group of patients will receive an intradiscal injection of Hydrocortancyl.
Drug: Hydrocortancyl.
Patients will receive an intradiscal injection of hydrocortancyl.
Sham Comparator: Local anaesthetic
A group of patients will receive an intradiscal injection of Lidocaine.
Drug: Lidocaine

Detailed Description:
This is a randomized, controlled, single-blind with two arms (anaesthetic versus corticoids) trial.

Ages Eligible for Study:   18 Years to 80 Years   (Adult, Senior)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No

Inclusion Criteria:

  • Age between 18 and 80 years
  • Signed Informed consent
  • Low back pain for more than 6 months associated with Modic I discopathy (diagnosed by MRI)

Exclusion Criteria:

  • Past history of lumbar surgery
  • Patient under anticoagulant or antisludge treatment, or with coagulation troubles
  • Patient with unbalanced diabetes mellitus (blood glucose > 1.30 g/l)
  • Patient with unstabilized high blood pressure (> 160/95 mmHg)
  • Patient with evolving infection
  • Patient with iodine allergy or one of the Hydrocortancyl® or Lidocaine components
  • Porphyria, hypersensitivity to local anaesthetic
  • Patient with sphincter troubles showing a cauda equine syndrome
  • Untreated psychotic state
  • Pregnant women or of childbearing age without effective contraception means
  • Impossible 6 months follow-up
  • Participation to another trial
  • Vulnerable persons protected by the law
  • Persons under guardianship
  • Persons unable to express their consent
  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its identifier: NCT01694134

Contact: Isabelle Tavares, MD +334 67 33 88 26

Hospital University of Montpellier Recruiting
Montpellier, France, 34000
Contact: Isabelle Tavares, MD    +334 67 33 88 26   
Principal Investigator: Isabelle Tavares, MD         
Sponsors and Collaborators
University Hospital, Montpellier
  More Information

Responsible Party: University Hospital, Montpellier Identifier: NCT01694134     History of Changes
Other Study ID Numbers: 8833
Study First Received: September 22, 2012
Last Updated: May 31, 2016

Keywords provided by University Hospital, Montpellier:
Modic I
Local Anaesthetic
Intradiscal injection

Additional relevant MeSH terms:
Back Pain
Low Back Pain
Intervertebral Disc Displacement
Intervertebral Disc Degeneration
Neurologic Manifestations
Nervous System Diseases
Signs and Symptoms
Spinal Diseases
Bone Diseases
Musculoskeletal Diseases
Pathological Conditions, Anatomical
Anesthetics, Local
Prednisolone acetate
Methylprednisolone acetate
Methylprednisolone Hemisuccinate
Prednisolone hemisuccinate
Prednisolone phosphate
Central Nervous System Depressants
Physiological Effects of Drugs
Sensory System Agents
Peripheral Nervous System Agents
Anti-Arrhythmia Agents
Voltage-Gated Sodium Channel Blockers
Sodium Channel Blockers processed this record on May 23, 2017