Comparison of the Stiffness of the Lumbar Back Muscles Between Low Back Pain and Healthy Controls
NCT ID: NCT03750474
Last Updated: 2018-11-23
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
UNKNOWN
NA
52 participants
INTERVENTIONAL
2018-12-01
2020-05-01
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Intra- And Inter-operator Reliability Of Isometric Back And Abdominal Muscle Strength Testing In Healthy Controls And Persons With Nonspecific Chronic Low Back Pain.
NCT03571880
the Role of MRI in Evaluation of Low Back Pain
NCT06766240
Feasibility of a One-day-and-a-half for Patients With Low Back Pain
NCT04133818
Load Quantitative MRI Study of Incipient LBP Patients.
NCT01916811
Selection of Chronic Low Back Pain Patients for Neurotomy Surgery Radiofrequency
NCT05624307
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Over the last decade, imaging techniques have become very helpful to characterize the biomechanical properties of tissues in vivo. Today, supersonic shear wave elastography (SWE) allows real time mapping of the elastic shear modulus. Also, magnetic resonance allows mapping and quantifying stiffness within a large volume of tissue. Elastography is efficient in the characterization of passive and active muscle forces, in highlighting the influence of muscle stiffness on joint stiffness and in showing stiffness changes related to muscle diseases Imaging plays a key role in the management of CLBP; It allows to reach specific radiological diagnosis such as tumor, inflammatory, or arthritis. However, in many cases, MRI did not find a specific cause to low back pain and the low back pain is reported as "non-specific". Myofascial disorders are also responsible for non-specific CLBP.
The main objective of this study is to compare the shear modulus of the main lumbar back muscles (erector spinae and multifidus) between patients with low back pain and healthy controls.
Second objectives are to assess: the relationship between the stiffness of the back muscles and clinical stiffness, the influence of age and sex on the elasticity of the back muscles, the relationship between the surface of the paravertebral muscles and the elasticity; the relationship between the elasticity of the hypaxial muscles (in front of the spine) and the epaxial muscles (behind the spine =back muscles), the relationship between fatty infiltration and elasticity of the back muscles, the relationship between inflammation / edema of back muscles and stiffness of the back muscles, the influence of the muscular stretching on the elasticity of the paravertebral muscles, the difference of elasticity in the direction of the muscle fibers (oblique coronal) and perpendicular (axial), the stiffness difference the between the right and left muscles, the role of different postures on muscle elasticity, the relationship between the elasticity of the back muscles and the intensity and type of pain, the relationship between the elasticity of the paravertebral muscles and disco-vertebral and / or posterior apophyseal pathology.
The inclusion of 26 patients and 26 controls will demonstrate a difference in mean elasticity modulus of 1.1 standard deviation (between patients and controls), with 90% and an alpha risk of 5%.
Patients will undergo an MRI (sagittal Short Inversion Time Inversion Recovery (STIR) and T1, coronal STIR and axial T1) in the management of low back pain. At the end of their examination, two elastography-sequences will be performed (axial and coronal plane). After the MRI, the patient will undergo a shear wave sonoelastography.
Healthy controls will undergo an MRI (sagittal T1 and T2) and two elastography-sequences (axial and coronal plane). After the MRI, the patient will undergo a an shear wave sonoelastography .
Healthy controls will be recruited in the hospital and university. Patients will be included when the appointment for MRI was made. Signed informant consent will be obtained after oral and written information.
The data manager will be trained to complete the case report form (CRF) and questionnaires; CRF and questionnaire. The entries that are not done according to procedure will result in inaccurate research data and inadequate source documentation. All data collected in the CRF will be scanned in a timely manner, then saved in an Exel folder, and initialized and dated by the data manager. Scanned data will be saved to the local database and on Universal Serial Bus (USB) disk. Computers designated for data entry, export and scanning will be password protected.
Data reported as missing, unavailable, non-reported, uninterpretable, or considered missing because of data inconsistency or out-of-range results were excluded.
Descriptive and comparative statistics will be done. The shear modulus will be compared between cases and controls using a Student's test (or Wilcoxon's test). For the secondary criteria, the comparison between qualitative variables will be made using the Chi² test, the comparison between a quantitative variable and a qualitative variable with a Student test (or Wilcoxon) or a one-way analysis of variance ( or Kruskal-Wallis test), the association between quantitative variables with the calculation of the Pearson (or Spearman) coefficient, depending on the conditions of application.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
NON_RANDOMIZED
PARALLEL
DIAGNOSTIC
NONE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
patient with chronic low back pain
magnetic resonance elastography and shear wave elastography of the back muscles
magnetic resonance elastography and shear wave elastography
magnetic resonance elastography and shear wave elastography of the back muscles
healthy controls
magnetic resonance elastography and shear wave elastography of the back muscles
magnetic resonance elastography and shear wave elastography
magnetic resonance elastography and shear wave elastography of the back muscles
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
magnetic resonance elastography and shear wave elastography
magnetic resonance elastography and shear wave elastography of the back muscles
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* Lumbar MRI without planned injection in chronic low back pain assessment
* Age between 18 and 80 years
* Ability to keep still in an MRI machine
* No contraindication to MRI
* No major sporting activity within 48 hours prior to the exam
* Informed and written consent"
* No lumbar pain symptomatology, no lumbar static disorder, known neuromuscular pathology
* Age between 18 and 80 years
* Ability to keep still in an MRI machine
* No contraindication to MRI
* Informed and written consent
Exclusion Criteria
* Intercurrent illness that may interfere with exam results
* Concomitant use of medications that may alter muscle metabolism
* Need to inject contrast during MRI
* Non-affiliation to a social security
* Minors, protected adults, persons unable to consent, persons under the protection of justice
18 Years
80 Years
ALL
Yes
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Assistance Publique - Hôpitaux de Paris
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Maud CREZE, PHU
Role: PRINCIPAL_INVESTIGATOR
APHP
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Hopital Bicêtre - Radiology Department
Le Kremlin-Bicêtre, , France
Countries
Review the countries where the study has at least one active or historical site.
Central Contacts
Reach out to these primary contacts for questions about participation or study logistics.
Facility Contacts
Find local site contact details for specific facilities participating in the trial.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
2017-A02799-44
Identifier Type: OTHER
Identifier Source: secondary_id
K180403J
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.