Sjogrens Screening Dry Eye Study
Brief description of study
The purpose of this study is to study and validate a new tool for screening dry eye patients for possible Sjogren's Syndrome (SS). This tool is composed of a combination of questionnaire responses and standard dry eye exam findings. Participating centers (Penn and Johns Hopkins University) will collect clinical data and specimens from dry eye patients who may or may not have SS. Specimens will include tears, saliva, whole blood, serum and labial minor salivary gland (lip) biopsy specimens. All individuals will participate in a standard evaluation protocol including an oral, ocular and physical examination, objective tests for dry eyes and dry mouth and, whenever necessary, a labial minor salivary gland biopsy. It is proposed that 40-50 patients per year at each site will be enrolled for the next 3-4 years at each site.
Detailed description of study
Study participation involves a 1.5-hour visit consisting of a dry eye examination, blood draw, salivary flow rate test, and answering questionnaires. Based on the results of this visit, certain participants may be invited to return for a lip biopsy.
Qualified participants will receive $50 for completion of the initial visit and $150 for completion of the lip biopsy.
Eligibility of study
You may be eligible for this study if you meet the following criteria:
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Conditions:
dry eye. dry eyes
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Age: Between 18 Years - 99 Years
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Gender: All
- Dry eyes for at least 3 months
- Aged 18 or older
- No previous diagnosis or evaluation for Sjogren’s syndrome
- No rheumatologic diseases
- No history of refractive surgery (LASIK, PRK/ASA)
- No history of head or neck radiation or chemotherapy
- No pre-existing lymphoma
- Not being treated for glaucoma with daily eye drops
Updated on
02 Jul 2023.
Study ID: 828400