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Autologous Serum Efficacy Study in Patients With Severe Dry Eye

Dry Eye Clinical Trial

Official title:
Autologous Serum Efficacy Study in Patients With Severe Dry Eye

Clinical Trial Summary

The purpose of this study is to compare the reduction in symptomatology of patients with severe dry eye treated with autologous serum and conventional artificial tears.

Clinical Trial Description

Severe dry eye remains an important and frequent eye disease, that reflects in a severe impairment of the patient´s life quality. Up to date there is no ideal therapy for this condition. Few studies have reported some kind of improvement in different parameters related to dry eye with the use of autologous serum, but no one has considered the patient´s symptoms with a systematic and validated evaluation method. ;

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Crossover Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Treatment

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT00779987
Study type Interventional
Source University of Chile
Contact
Status Completed
Phase Phase 2
Start date October 2008
Completion date December 2008
View Details
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