A Prospective Cohort Study of Patients Suffering From Hand Osteoarthritis Symptoms
Recruiting · NCT03650673 · Interventional (participants receive a specific treatment) · Lead sponsor: University Hospital, Montpellier
View the official record on ClinicalTrials.gov →Interventions studied
Identification of subgroups of patients with early AD with risk of progression
What this trial is about
The late-stage forms of degenerative osteoarthritis (OA) are very debilitating and less affordable to therapy. The main objective is to identify early onset symptoms of hand OA patients through imaging techniques (such as ultrasound and MRI). Our primary endpoint is to specify patients with high risk of radiological profression (X-ray).
Who can take part
Age range
18 Years to 60 Years
Sex
All (male and female)
Healthy volunteers
No - a diagnosis or condition is required
Phase
Not applicable (e.g. observational or device study)
Study type
Interventional (participants receive a specific treatment)
Inclusion criteria
- \- Early digital osteoarthritis must combine the clinical AND radiological definition.
- Clinical definition:
- At least one of the following 4 criteria: Pain or stiffness or swelling or deformity of a digital joint (IPP and / or IPD) A breach of at least one PPI and / or IPD Age under 60 at the time of the first symptoms Clinical symptoms have been changing for less than 3 years
- Radiographic definition:
- The presence of the achievement of at least one PPI and / or IPD. Presence of at least two of the following three criteria: pinching, marginal subchondral condensation, marginal osteophyte Erosion on radiography is not an
Exclusion criteria
- \- Consent form signed
- Exclusion criteria:
- patients suffering from rheumatoid arthritis, rheumatoid psoriasis or any other inflammatory rheumatism
- patients suffering from metabolic diseasis such as gout, hemochromatosis, Wilson's disease; or from congenital disease such as displasie, osteogenesis,
- Presence of advanced radiographic osteoarthritis based in Kellgreen Lawrence score (=4) in one joint among the 10 previous sites.
- Not able to provide a sample of blood for any reasons
- MRI contraindication
- Being in exclusion period determined by another previous study
- Subject non affiliated to social insurance
- Pregnant or lactating women
- Vulnerable people based in L1121-5 article of CSP
- Elderly subject or protected subjects disabled to give their consent
- Subjects private of freedom by court or administrative order
Where it is running
1 location listed.
- Department of Rheumatology, CHU Montpellier - Montpellier, France