Survey on lupus symptoms for patients
Part of Immune system & allergy, Skin clinical trials.
This study asks people with lupus to share their opinions through surveys to help researchers agree on better ways to measure the disease. Your input can help improve future lupus treatments.
Summary written for real people, not researchers, by Clin2.
Who can take part
- You are 18 years old or older.
- You have been diagnosed with systemic lupus erythematosus (SLE).
- You can read and understand one of these languages: English, Spanish, French, Italian, Portuguese, Japanese, Arabic, Korean, Hebrew, German, or Chinese.
- You have access to email and the internet to participate.
Quick eligibility check
Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.
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This trial collects health data from people recently diagnosed with lupus to improve treatment and care. It is a registry study, not a drug-testing trial, and aims to understand how patients fare over time.
This study creates a registry for people with lupus and their families. It helps researchers learn more about lupus and improve care. You or your child can join if you have a lupus diagnosis.
This study keeps a long-term record of people with lupus (systemic lupus erythematosus) and collects samples so researchers can study the disease better. You may be able to join if you meet lupus diagnosis criteria, are not pregnant, and can follow the study visits and consent process.
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