Spinal Surgery Clinical Trial
— DISCO-PROPOfficial title:
Evaluation of the Prevalence of Germs Slow Growth in the Intervertebral Disc (IVD) During Spinal Surgery: a Single-center Prospective Observational Study
Verified date | August 2016 |
Source | Assistance Publique - Hôpitaux de Paris |
Contact | n/a |
Is FDA regulated | No |
Health authority | France: Ministry of Health |
Study type | Observational |
Low back pain is one of the most frequent reasons for consultation in rheumatology. There is
a strong correlation between low back pain, and the presence of a type of Modic 1 signal on
MRI.
The anomaly Modic 1 results in a hypointense signal T1-weighted images and hyperintense on
T2-weighted sequences (including T2 STIR and / or Fat Sat) and contrast enhancement of the
endplates after gadolinium injection; it corresponds to a replacement of normal cancellous
bone of fibrovascular tissue.
The origin of this inflammatory process Modic 1 into the vertebra is still unknown.
infectious hypothesis was raised, including contamination by germs called "slow-growth" such
as Propionibacterium acnes (PA).
Many studies interesting Bacteriological analysis of disc material found the presence of
bacteria (prevalence between 0 and 54%).
A recent clinical trial evaluating the efficacy of antibiotic treatment compared to placebo
in low back pain with Modic 1; a show effectiveness of this treatment on the different
clinical parameters evaluated.
However skin contamination is not formally excluded, particularly in patients previously
infiltrated (including epidural).
Our hypothesis is that the slow-growing bacteria are not involved in Modic 1 type of disc
disease, and the possible presence of PA or other slow-growing bacteria in samples obtained
discal posterior approach would be related to intraoperative contamination or during
preoperative spinal infiltrations The main objective is to assess the prevalence of germs
slow growth in the intervertebral disc in the spinal surgery by anterior disc disease in
type 1 Modic.
Status | Completed |
Enrollment | 80 |
Est. completion date | December 2015 |
Est. primary completion date | December 2015 |
Accepts healthy volunteers | No |
Gender | Both |
Age group | 18 Years to 75 Years |
Eligibility |
Inclusion Criteria: - Major patients accepted to participate in the study and who signed an informed consent. - Patients with low back pain lasting for more than 6 months, disabling, with disc disease type 1 Modic eligible for a disc prosthesis or arthrodesis anterior approach. - Patients underwent surgery for nerve root pain by disc herniation on MRI viewable with a radio-clinical concordance with or without Modic 1 disc disease in the operated disc Exclusion Criteria: - Lumbar spine surgery history within 12 months and / or presence of osteosynthesis material. - Immunocompromised patients (HIV, cancer, immunosuppressive treatment, lupus, chronic infection, ...) - Patients previously treated with antibiotics exceeding 15 days during last 3 months prior enrollment for a period |
Observational Model: Cohort, Time Perspective: Prospective
Country | Name | City | State |
---|---|---|---|
France | Henri Mondor Hospital | Creteil |
Lead Sponsor | Collaborator |
---|---|
Assistance Publique - Hôpitaux de Paris |
France,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Presence or lack of germs slow growth in disc by standard culture and molecular biology technique (16S RNA). | Visit 2 (surgery day) | No |
Status | Clinical Trial | Phase | |
---|---|---|---|
Completed |
NCT05023850 -
Comparing Thoracolumbar Interfascial Plane Block With Erector Spinae Plane Block
|
N/A | |
Completed |
NCT01251042 -
Comparison Between Return and Wastage of Your Own Blood, Collected During Spinal Surgery, for Verification of Safety When Returning Blood
|
N/A | |
Completed |
NCT01356082 -
CNAP™ Monitor Study
|
N/A | |
Completed |
NCT06323694 -
Quality of Life, Expectations, Thoughts and Fears of Patients on the Waiting List for Spinal Surgery
|
||
Recruiting |
NCT04370951 -
Efficacy of the Erector Spinae Plane Block in Posterior Thoraco- Lumbar Spinal Decompression Surgery
|
N/A | |
Completed |
NCT03069794 -
Effect of Spinal Surgery on the Posture and the Balance of the Patients Reached of Spinal Pathologies
|
N/A | |
Recruiting |
NCT02595788 -
Haemodynamic Changes During Anaesthesia in the Prone Position, Evaluated Using Transoesophageal Ultrasound
|
N/A | |
Completed |
NCT01855542 -
The Aim of This Investigation is to Compare the Influence of 0.9% Saline and Plasmalyte Solution on Acid-base Balance and Electrolytes in Healthy Patients Undergoing Major Spine Surgeries.
|
N/A | |
Not yet recruiting |
NCT01299818 -
Assessment of Central Pain in Patients Who Undergo Spinal Surgery and Influence in Surgery Outcome
|
N/A | |
Recruiting |
NCT05417100 -
Understanding How Methadone Treatment During Surgery Affects Pain Levels and the Need for Pain Medications After Surgery
|
Phase 3 | |
Completed |
NCT00491608 -
Immunogenicity and Safety Study of Topical Recombinant Thrombin in Surgical Hemostasis
|
Phase 3 | |
Terminated |
NCT03160170 -
Efficacy of Suction Enabled Retraction Device
|
N/A | |
Not yet recruiting |
NCT06466083 -
Correlation Analysis of POD and PND in Elderly Spinal Surgery Patients Based on Rs-fMRI
|
||
Recruiting |
NCT06451627 -
Esketamine on Postoperative Sleep Disturbance of Patients Undergoing Spinal Surgery
|
N/A | |
Not yet recruiting |
NCT04922359 -
Effect of Perioperative Lidocaine on Gastrointestinal Function Recovery After Lumbar Spine Surgery in Adults
|
N/A | |
Recruiting |
NCT04189172 -
MiDura-Study (Neuro-Patch in Duraplasty)
|
||
Recruiting |
NCT05553028 -
Study Comparing Arthrodesis Technique of Thoracic and/or Lumbar Spine by Posterior Approach Performed by Robot-assisted Surgery (Robot Mazor X Stealth ™) Versus Conventional Surgery
|
N/A | |
Completed |
NCT06118489 -
Effects of Different Anesthetic Gases on Hemodynamics, Arterial Oxygenation and Lung Mechanics
|
||
Recruiting |
NCT03512379 -
Clinical Trial for the Application of Robotic System in Spinal Surgery
|
N/A | |
Recruiting |
NCT03501810 -
Study Assessing Safety and Performance of OrtoWell Distractor in Patients Undergoing Spinal Surgery
|