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Evaluation of FID 114657 in Sjogren's Syndrome Subjects

Sjogren's Syndrome Clinical Trial

Clinical Trial Summary

The primary objective of this study is to assess the overall Sjogren's Syndrome subject's preference for a particular product. Dry eye symptom relief will also be evaluated based on clinical evaluation and a set of subject questionnaires.

Clinical Trial Description

n/a

Study Design

Allocation: Non-Randomized, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT01079871
Study type Interventional
Source Alcon Research
Contact
Status Completed
Phase N/A
Start date February 2010
View Details
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