PSFS: Penn SICCA Follow-up Study
Study Details
Study Description
Brief Summary
This study will involve the collection of follow-up data for patients who previously participated in the Sjogren's International Clinical Collaborative Alliance (SICCA) study at the University of Pennsylvania. Clinical data and specimens will be collected from subjects with objective evidence of dry eye who were or were not diagnosed with Sjogren's syndrome at the time of their initial participation in the SICCA study. Specimens will be collected from participants which will include tears, saliva, whole blood, serum, DNA and possible labial minor salivary gland biopsies when indicated. 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. The biopsy requirement is waived for those who have already had positive lip biopsies in the past.
| Condition or Disease | Intervention/Treatment | Phase |
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Detailed Description
General study design: This is a single center study that involves follow-up of patients who previously participated in the Sjogren's International Collaborative Clinical Alliance (SICCA) at the University of Pennsylvania. Objective evaluation of salivary function will be done by collecting unstimulated whole and stimulated parotid saliva. Objective evaluation of lacrimal function will be performed using the Schirmer test I, Lissamine Green staining, and determining tear break-up time. In a subset of patients, when indicated an objective evaluation of lymphocytic infiltration of the minor salivary glands will be performed by histologic analysis of labial salivary gland biopsies. Serum autoantibody profiles will be determined. In addition, specimens such as biopsies, saliva, sera, conjunctival cells, and tears will be collected. Standardized questionnaires will be used to gain health information.
Study Design
Outcome Measures
Primary Outcome Measures
- Collection of specimens and clinical information [2 years]
To collect specimens (saliva, tears, conjunctival cells, and blood) and clinical information on dry eye patients with or without Sjogren's syndrome
Secondary Outcome Measures
- Ocular surface exam findings [2 years]
Characterize the clinical features of the ocular and oral components of dry eye patients with or without Sjogren's syndrome.
- Serologic testing [2 years]
Characterize the laboratory, including serologic (including autoantibodies), features of dry eye patients with or without Sjogren's syndrome.
Eligibility Criteria
Criteria
Inclusion Criteria:
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Previously participated in the SICCA study at Penn
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Be 18 years or older
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Have signed an IRB consent form agreeing to the terms of the study
Exclusion Criteria:
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Did not previously participate in SICCA study at Penn
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Under the age of 18 years
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | Scheie Eye Institute | Philadelphia | Pennsylvania | United States | 19104 |
Sponsors and Collaborators
- University of Pennsylvania
Investigators
- Principal Investigator: Vatinee Bunya, MD, Scheie Eye Institute
Study Documents (Full-Text)
None provided.More Information
Publications
None provided.- 827285