- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01688219
Immune Response in the SAPHO Syndrome
September 18, 2012 updated by: Assistance Publique - Hôpitaux de Paris
Immune Mechanisms During SAPHO Syndrome and Treatment by Etarnecept
The aetiology of SAPHO syndrome seems to involve genetic, infectious and immunological components.
The investigators examined innate and adaptative immune responses in SAPHO syndrome as compared with psoriatic arthritis and rheumatoid arthritis.
Study Overview
Status
Completed
Conditions
Study Type
Observational
Enrollment (Actual)
39
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
1 year to 70 years (Child, Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Probability Sample
Study Population
SAPHO syndrome patients
Description
Inclusion Criteria:
- Clinical diagnosis of SAPHO syndrome
- Must have bone lesions
Exclusion Criteria:
- Infliximab treatment
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Observational Models: Cohort
- Time Perspectives: Prospective
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
IL-8 production by PMN
Time Frame: 24 h
|
24 h
|
Secondary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
TNFalpha production by PMN
Time Frame: 24 h
|
24 h
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Study Director: Gilles Hayem, PhD, Assitance Publique-Hopitaux Paris
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
November 1, 2005
Study Completion (Actual)
May 1, 2008
Study Registration Dates
First Submitted
September 14, 2012
First Submitted That Met QC Criteria
September 18, 2012
First Posted (Estimate)
September 19, 2012
Study Record Updates
Last Update Posted (Estimate)
September 19, 2012
Last Update Submitted That Met QC Criteria
September 18, 2012
Last Verified
October 1, 2007
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 45896566645469
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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