Improving the Assessment of SLE Disease Activity
Sponsored by University Health Network, Toronto
About this trial
Last updated 8 years ago
Study ID
Status
Type
Placebo
Accepting
Not accepting
Trial Timing
Ended 7 years ago
What is this trial about?
What are the participation requirements?
Inclusion Criteria
Objective I: - ≥4 American College of Rheumatology (ACR) criteria or 3 ACR criteria plus a typical histological lesion of SLE on renal or skin biopsy - Clinician's diagnosis based on his/her assessment - Patients from the Toronto Lupus Clinic with regular follow-up, defined as having follow up visits at 3 and 6 months from the baseline visit (1st study visit). Objective II: • Participant in the BLISS-52 and BLISS-76 trials Objective III: - ≥4 American College of Rheumatology (ACR) criteria or 3 ACR criteria plus a typical histological lesion of SLE on renal or skin biopsy - Increase in SLEDAI-2K ≥4 - Clinician's diagnosis based on his/her assessment
Exclusion Criteria
Objective I and III: - Patients with missing follow up visits at 3 and 6 months from the baseline visit (1st study visit). - Patients with missing data in the charts for all visits. Objective II: • Participants who did not complete the trial and therefore have missing data points for primary endpoint measures