Clinical Trials Logo

Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04894253
Other study ID # 8263
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date June 7, 2021
Est. completion date February 2023

Study information

Verified date August 2022
Source University Hospital, Strasbourg, France
Contact Jean SIBILIA, MD
Phone 3 88 12 79 55
Email jean.sibilia@chru-strasbourg.fr
Is FDA regulated No
Health authority
Study type Observational [Patient Registry]

Clinical Trial Summary

The main objective is to study the impact of vaccination against Covid-19 on the specific humoral and cellular immune response (against SARS-CoV-2) and non-specific (evolution of the pathological immune system of the disease), in a lupus population. The secondary objective is to study the impact of lupus disease activity on the humoral and cellular response of patients following vaccination against SARS-CoV-2. The hypothesis is that disease activity and / or certain treatments used in lupus may interfere with the humoral and cellular immune response induced by vaccination against SARS-CoV-2.


Recruitment information / eligibility

Status Recruiting
Enrollment 30
Est. completion date February 2023
Est. primary completion date February 2023
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Adult subject (= 18 years old), male or female - Patient with systemic lupus according to ACR 1997 criteria - Patient followed by the National Reference Center "Rare Systemic Autoimmune Diseases" of the University Hospitals of Strasbourg - Patient who agreed to be vaccinated against SARS-CoV-2 - Subject having expressed his non-opposition to the research - Subject affiliated to a social health insurance protection scheme Exclusion Criteria: - Patient treated by: - Corticosteroids (> = 10mg / day) - Immunosuppressant (azathioprine, mycophenolate mofetil, cyclophosphamide) to control lupus activity - A biomedicine targeting B cells (rituximab, belumimab). - Inability to provide informed information about the subject (subject in an emergency, difficulty in understanding the subject, etc.) - Subject under safeguard of justice - Subject under guardianship

Study Design


Related Conditions & MeSH terms


Intervention

Biological:
SRAS-CoV-2 vaccination immunological response
Follow for 18 months a single group of 30 patients with systemic lupus after their SRAS-CoV-2 vaccination. Intervention includes immunological analysis on additional volume of blood collected as part of routine care.

Locations

Country Name City State
France University Hospital of Hautepierre 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 Investigation of the immune response following vaccination against SARS-CoV-2 Collection of clinical data and correlation with immunological analyzes of the biological samples 3 or 4 weeks
Primary Investigation of the immune response following vaccination against SARS-CoV-2 Collection of clinical data and correlation with immunological analyzes of the biological samples 3 months
Primary Investigation of the immune response following vaccination against SARS-CoV-2 Collection of clinical data and correlation with immunological analyzes of the biological samples 6 months
Primary Investigation of the immune response following vaccination against SARS-CoV-2 Collection of clinical data and correlation with immunological analyzes of the biological samples 12 months
Primary Investigation of the immune response following vaccination against SARS-CoV-2 Collection of clinical data and correlation with immunological analyzes of the biological samples 18 months
Secondary Study the impact of lupus disease activity on SARS-CoV-2 vaccine immune response Measurement of lupus disease activity by a validated score (SLEDAI) at the time of vaccination and follow-up. 3 or 4 weeks
Secondary Study the impact of lupus disease activity on SARS-CoV-2 vaccine immune response Measurement of lupus disease activity by a validated score (SLEDAI) at the time of vaccination and follow-up. 3 months
Secondary Study the impact of lupus disease activity on SARS-CoV-2 vaccine immune response Measurement of lupus disease activity by a validated score (SLEDAI) at the time of vaccination and follow-up. 6 months
Secondary Study the impact of lupus disease activity on SARS-CoV-2 vaccine immune response Measurement of lupus disease activity by a validated score (SLEDAI) at the time of vaccination and follow-up. 12 months
Secondary Study the impact of lupus disease activity on SARS-CoV-2 vaccine immune response Measurement of lupus disease activity by a validated score (SLEDAI) at the time of vaccination and follow-up. 18 months
See also
  Status Clinical Trial Phase
Completed NCT03749044 - ASA Patterns for Prevention of Preeclampsia in SLE Pregnancies N/A
Completed NCT03218033 - Use of Social Media to Improve Medication Adherence in Adolescents and Young Adults With Systemic Lupus N/A
Not yet recruiting NCT03752983 - Chemokine (CXCL13) as Anew Marker in Diagnosis of SLE
Recruiting NCT03819777 - Volatile Organic Compounds (VOCs) as a Biomarker in Immune-mediated Pulmonary Arterial Hypertension (PAH)
Not yet recruiting NCT03164720 - SSerum/Urinary Monocyte Chemoattractant Protein-1 Level as a Marker for Lupus Nephritis
Completed NCT03762824 - Combined Pneumococcal Conjugate and Polysaccharide Vaccination in Inflammatory Rheumatic Disease Phase 4
Terminated NCT01738360 - Phase 2a Study Evaluating the Arsenic Trioxide (ATO) in Systemic Lupus (SLE) (Protocol LUPSENIC) Phase 2
Completed NCT03430388 - Yellow Fever Vaccine in Patients With Rheumatic Diseases N/A
Completed NCT04108611 - Immune Adsorption Role in Treatment of Resistant Lupus N/A
Not yet recruiting NCT04256577 - Serum Ceramides Level in Systemic Lupus Erythematosus (SLE) Patients as a Novel Marker for Renal Impairment
Completed NCT03540823 - Evaluation of Influenza A/H3N2 Vaccine in Patients With Rheumatologic Diseases Phase 4