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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT04799730
Other study ID # Soh-Med-21-03-01
Secondary ID
Status Not yet recruiting
Phase
First received
Last updated
Start date May 2021
Est. completion date May 2022

Study information

Verified date March 2021
Source Sohag University
Contact Asmaa A Ibrahim, Master
Phone 01032138809
Email smaibrahim2019@gmail.com
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The objective of this study is to estimate the possible role of CD184 in the pathogenesis of SLE; comparing its level among SLE cases to healthy controls.


Description:

Detection of CXCR4 (CD184) expression on CD19+ B cells by flow cytometry in patients of SLE, comparing its level in the development of lupus activity and pathogenic process of SLE internal organ involvement/ mucocutaneus and/or musculoskeletal involvement. Identify this correlation will be useful for clarifying other accessory factors to improve the diagnosis, better treatment strategy, follow up as well as prognosis for these patients


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 100
Est. completion date May 2022
Est. primary completion date November 2021
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 16 Years to 60 Years
Eligibility Inclusion Criteria: - Confirmed SLE patients diagnosed and fulfilled the SLE classification criteria according to the 2019 ACR/EULAR classification criteria for SLE (Aringer et al., 2019) - Willing and agreed to be included in the study. Exclusion Criteria: - Childhood SLE. - SLE-patients will refuse to consent to this study. - Other autoimmune diseases. - Known or suspected malignancies, especially B cell lymphoma.

Study Design


Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Sohag University

Outcome

Type Measure Description Time frame Safety issue
Primary changes in the expression of CD184(CXCR4) expression in circulating B cells Flow cytometry analysis of chemokine receptor (CXCR4):Human peripheral-blood mononuclear cells (PBMCs) labeling with CXCR4 antibody will be performed in the same day after taking blood samples and subsequent measurement of the CXCR4 mean fluorescence intensity (MFI) by flow cytometry. MFI of the anti-chemokine receptor (CXCR4) staining will be calculated according to statistical thresholds set in reference to staining with negative control antibodies. The patient's CXCR4 on CD19+ B cells expression or mean MFI will be further compared to the MFI of the simultaneously performed age-matched controls samples and other subgroups of SLE patients. 6 months
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