CTHRC1 Abiomarker in Rheumatoid Arthritis Diagnosis
CTHRC1 Apromising Biomarker in Rheumatoid Arthritis Diagnosis
1 other identifier
observational
90
0 countries
N/A
Brief Summary
The purpose of the study is to determine whether plasma levels of the collagen triple helix repeat containing (CTHRC1) protein can serve as a blood-based biomarker for diagnosis of rheumatoid arthritis (RA) ,and furthermore its correlation with disease activity.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for all trials
Started Oct 2019
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
First Submitted
Initial submission to the registry
September 9, 2019
CompletedFirst Posted
Study publicly available on registry
September 11, 2019
CompletedStudy Start
First participant enrolled
October 1, 2019
CompletedPrimary Completion
Last participant's last visit for primary outcome
October 1, 2020
CompletedStudy Completion
Last participant's last visit for all outcomes
December 1, 2020
CompletedSeptember 18, 2019
September 1, 2019
1 year
September 9, 2019
September 16, 2019
Conditions
Outcome Measures
Primary Outcomes (1)
CTHRC1 Apromising biomarker in rheumatoid arthritis diagnosis
measurement of levels of CTHRC1 in rheumatoid arthritis patients
one year
Interventions
measurment of levels of CTHRC1 in patients diagnosed as RA
Eligibility Criteria
measurement of CTHRC1in RA patints
You may qualify if:
- Patients diagnosed as RA.
- Patients ( \>18)who are age and sex matched with the controls
You may not qualify if:
- Other Rheumatologic diseases. .Patients with malignancy . .Patients with hepatic disease .
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Related Publications (1)
Myatt GL, Ecobichon DJ, Greenhalgh R. Fenitrooxon and S-methyl fenitrothion: acute toxicity and hydrolysis in mammals. Environ Res. 1975 Dec;10(3):407-14. doi: 10.1016/0013-9351(75)90036-5. No abstract available.
PMID: 2462BACKGROUND
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Central Study Contacts
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Principal investigator
Study Record Dates
First Submitted
September 9, 2019
First Posted
September 11, 2019
Study Start
October 1, 2019
Primary Completion
October 1, 2020
Study Completion
December 1, 2020
Last Updated
September 18, 2019
Record last verified: 2019-09