Evaluating the Efficacy of Para-discal Infiltration in Patients With Lateralized MODIC 1 Inflammatory Disc Disease

NCT ID: NCT05615597

Last Updated: 2024-05-29

Basic Information

• Recruitment Status: RECRUITING
• Clinical Phase: NA
• Total Enrollment: 30 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2022-12-22
• Study Completion Date: 2025-12-22

Brief Summary

Degenerative disc disease (DDD) is a major cause of chronic low back pain (> 40%). It can be defined by specific magnetic resonance imaging (MRI) features, with a strong correlation between pain and the inflammatory aspect of the disc, resulting in active disc disease (AD). The Modic classification based on MRI of the lumbar spine is considered a reference.

The management of low back pain in patients with inflammatory disc disease generally involves intra-disc corticosteroid infiltration, which has been widely proven to be effective in reducing pain [4-6]. However, this procedure can be painful and invasive and sometimes impossible to perform due to severe disc impingement.

The aim of this study is to evaluate the efficacy on pain of para-disc infiltration of corticosteroids in contact with the inflammatory MRI signal abnormality (Modic 1) when it is lateralized.

This variant of infiltration is easier to perform (no catheterisation of the disc and therefore quicker), would entail less risk of disc infection and would be accessible to more radiologists.

It is already practised but, to our knowledge, has never been the subject of a study to evaluate its effectiveness on pain.

If successful, more patients could be treated and the range of treatment could be extended.

Conditions

Degenerative Disc Disease; Inflammation; Low Back Pain

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Para-discal infiltration

Single arm study

Group Type: OTHER

Para-discal injection of corticoid

Intervention Type: PROCEDURE

In this pilot study, all patients underwent the same procedure: a corticosteroid infiltration via a para-discal approach. The infiltrations were performed under CT or scopy.

Interventions

Para-discal injection of corticoid

In this pilot study, all patients underwent the same procedure: a corticosteroid infiltration via a para-discal approach. The infiltrations were performed under CT or scopy.

Intervention Type: PROCEDURE

Eligibility Criteria

Inclusion Criteria

• Patient 18 years of age or older
• Patient with Modic I lateralized disc disease seen on an MRI less than 6 months old.
• Chronic medial or lateralized (same side as MODIC 1) low back pain for at least 3 months with a mean pain intensity ≥ 40/100 mm on a VAS.
• Effective contraception for women of childbearing age, at least 6 months after injection (surgical sterilisation, approved hormonal contraceptives, barrier methods, intrauterine intrauterine device)

Exclusion Criteria

• Patient with MODIC 1 in both underlying and overlying vertebral spaces.
• Patient with an inflammatory signal abnormality of the vertebral body plateau related to non-mechanical pathology (e.g. spondyloarthritis).
• Patients with a history of lumbar spine surgery.
• Patient with suspected spondylodiscitis or other infection.
• Patients on anticoagulant or antiaggregant therapy, or with a coagulation disorder.
• Patients with an allergy to iodine or to any of the components of Xylocaine.
• Patients with an allergy to prednisolone or to any component of Hydrocortancyl® or Dexamethasone®..
• Patient with severe uncontrolled disease (i.e. cardiac gastrointestinal, neurological, endocrine, autoimmune) that limits patient safety (as determined by the safety (as judged by the investigator).
• Prior to the treatment visit :

• current and recent morphine use (< 1 month)
• recent systemic or local corticosteroid therapy (< 1 month).
• Patient with sphincter disturbances indicative of cauda equina syndrome.
• Psychotic state not controlled by treatment
• Pregnancy (βHCG positive), breastfeeding
• Vulnerable patient protected by law
• Patient under guardianship or curatorship
• Patient participating in an interventional study
• Patient unable to read and/or write

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

University Hospital, Montpellier

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Arthur HAMEL-SENECAL, MD

Role: PRINCIPAL_INVESTIGATOR

Departement of Medical Imaging - Montpellier University hospital LAPEYRONIE Hospital

Locations

Departement of Medical Imaging

Montpellier, Occitanie, France

Site Status: RECRUITING

Countries

France

Central Contacts

Arthur HAMEL SENECAL, MD

Role: CONTACT

arthur.hamelsenecal@chu-montpellier.fr

0467338946 ext. +33

Catherine CYTEVAL, MD, PhD

Role: CONTACT

c-cyteval@chu-montpellier.fr

Facility Contacts

Celine ENGRAND

Role: primary

c-engrand@chu-montpellier.fr

Other Identifiers

RECHMPL22_0230

Identifier Type: -

Identifier Source: org_study_id