Clinical and Molecular Aspects of Early Osteoarthritis
1 other identifier
observational
65
1 country
1
Brief Summary
The etiology of osteoarthritis is varied, ranging from multifactorial, environmental to monogenic. In individuals in whom osteoarthritis appears earlier than in the general population, it is called early osteoarthritis. To our knowledge, there are no large-scale genetic studies on people with early osteoarthritis. The investigators therefore sought to study the causes of monogenic osteoarthritis in people suffering from early non-syndromic osteoarthritis. Material and method From 2013 to 2019, experts in constitutional bone disease sent patients with non-syndromic early osteoarthritis for genetic analysis to our center of competence for constitutional bone diseases. The sequencing of a panel of genes was carried out by NGS.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for all trials
Started Jan 2013
Longer than P75 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
January 1, 2013
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 1, 2019
CompletedStudy Completion
Last participant's last visit for all outcomes
January 1, 2020
CompletedFirst Submitted
Initial submission to the registry
February 7, 2020
CompletedFirst Posted
Study publicly available on registry
February 13, 2020
CompletedFebruary 13, 2020
February 1, 2020
6.9 years
February 7, 2020
February 11, 2020
Conditions
Keywords
Outcome Measures
Primary Outcomes (2)
identification of genetic mutation
sequencing out by NGS
1 day
number of genetic mutation
sequencing out by NGS
1 day
Eligibility Criteria
Patients with early osteoarthritis who have undergone genetic sequencing
You may qualify if:
- \- Patients with early osteoarthritis who have undergone genetic sequencing
You may not qualify if:
- \- Patients refusing to participate in research
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
UH Montpellier
Montpellier, 34295, France
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
David GENEVIEVE
Department of Medical Genetics
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- OTHER
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
February 7, 2020
First Posted
February 13, 2020
Study Start
January 1, 2013
Primary Completion
December 1, 2019
Study Completion
January 1, 2020
Last Updated
February 13, 2020
Record last verified: 2020-02