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Clinical Trial Details — Status: Terminated

Administrative data

NCT number NCT01889641
Other study ID # 5504
Secondary ID
Status Terminated
Phase N/A
First received June 25, 2013
Last updated September 7, 2017
Start date February 2014
Est. completion date April 2015

Study information

Verified date September 2017
Source University Hospital, Strasbourg, France
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Treatment of multisystemic forms of lupus displays severe side effects and limited efficacy, underscoring the need to better dissection of the pathogenic mechanisms. Concordant with preliminary data, IL26 signaling could be impaired in systemic lupus. Moreover, IL 26 could be a marker of the disease activity and then a potential therapeutic target. In the present study, serum IL 26 level in lupus patients and control will be measured.


Recruitment information / eligibility

Status Terminated
Enrollment 23
Est. completion date April 2015
Est. primary completion date April 2015
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- diagnostic of Lupus according to ACR criteria ( four criteria are necessary)

- age > 18 years old

Exclusion Criteria:

- treatment by cyclophosphamide, rituximab, belimumab in the year before inclusion study

Study Design


Related Conditions & MeSH terms

  • Diagnosis of Lupus According to ACR criteriaAgreement for the Blood Sampling

Locations

Country Name City State
France Les Hôpitaux Universitaires de Strasbourg Strasbourg Bas Rhin

Sponsors (1)

Lead Sponsor Collaborator
University Hospital, Strasbourg, France

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Assess serum IL-26 as a biological marker of SLE compared with sera from control subjects 2 years