NCT06759519Completed
Clinical and Demographic Features of Patients With Moderate to Severe Active Systemic Lupus Erythematosus in Russia
An Observational Multicenter Retrospective-prospective Study of Patients With Active Moderate to Severe SLE
Source: ClinicalTrials.gov · Last updated 9 Jul 2026
Brief summary (registry, in English)
This is a multicenter observational retrospective-prospective study consisting of retrospective and prospective phases. Trial will include 2 visits for obtaining the patient's demographic and clinical data: the 1st is retrospective and the 2nd is prospective. The study will involve approximately 50 sites of the Russian Federation; in each site about 20 patients will be recruited. The total planned size of study population will be approximately 1000 patients enrolled to the retrospective phase of the study, from which \~ 600 patients will be enrolled to the prospective phase.
- Status (registry)
- Completed
- Study type
- Observational
- Enrollment
- 637 (actual)
- First submitted
- 28 Aug 2024
- Start date
- 30 Aug 2024
- Primary completion date
- 19 Sept 2025
- Lead sponsor
- AstraZeneca
- Diseases
- Lupus (SLE)
- NCT number
- NCT06759519
What you commit to
- Study type: Observational
- Participants enrolled: 637
- From 30 Aug 2024 to the primary completion date, 19 Sept 2025
- 32 sites in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Prior treatment
- Regular use of genetically engineered biological drugs for SLE treatment within the last 24 months prior to inclusion;
- Current use of genetically engineered biological drugs for SLE treatment;
Other illness
- An acute or chronic disease that, in the opinion of the investigator, limits the ability of patient to provide data on his/her health or participate in this study or influence the interpretation of the results.
Other
- Participation in any interventional trial since the last patient's visit to the clinic;
- Presence of lupus nephritis class III/IV ± V at the moment of the last patient's visit to the clinic;
- Presence of neuropsychiatric lupus at the moment of the last patient's visit to the clinic.
- Additional exclusion criteria for the prospective phase are:
- Current participation in any interventional trial;
- Presence of lupus nephritis Class III/IV ± V at the moment of patient's visit;
- Presence of neuropsychiatric lupus at the moment of patient's visit;
Who the study is looking for
- Patients with the diagnosis of SLE (ICD code: M32) confirmed by medical records;
- Patients with availability of data of at least one visit to the clinic in the medical records in the last 24 months prior to inclusion;
- Age ≥ 18 years at the time of last patient's visit to the clinic.
- Additional inclusion criteria for the prospective phase are:
- Signed and dated written informed consent in accordance with ICH-GCP and local law prior to inclusion in the prospective phase of the study;
- Disease activity measured with SLEDAI-2K ≥ 6 despite of standard treatment at the time of inclusion in the prospective phase of the study
Sex: All · Does not accept healthy volunteers
Sites (32)
Sites in registry order. Pick your city on the disease page to sort them by distance.
This page is information, not medical advice. Discuss any trial with your doctor.