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Evaluation of Therapeutic Effect of Bandage Contact Lenses ( BCL) on Dry Eye Caused by Sjogren's Syndrome

NCT02147509 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 64

Last updated 2014-07-22

No results posted yet for this study

Summary

The purpose of this study is to evaluate the therapeutic effect and safety of therapeutic bandage contact lenses treating dry eye caused by Sjögren's syndrome.

Conditions

  • Sjögren's Syndrome Patients With Severe Dry Eye

Interventions

DRUG

0.02% Fm, SH

Sjogren's Syndrome patients with severe dry eye

DRUG

0.02% Fm, SH, 0.05% CsA

Sjogren's Syndrome patients with severe dry eye

OTHER

0.02% Fm, SH, tBCL

Sjogren's Syndrome patients with severe dry eye

DRUG

0.02% Fm, SH, AS

Sjogren's Syndrome patients with severe dry eye

Sponsors & Collaborators

  • Jinyang Li

    lead OTHER

Principal Investigators

  • Jinyang Li, MD,PhD · Eye Hospital, Wenzhou Medical College, China

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
SINGLE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Max Age
70 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2013-03-31
Primary Completion
2014-04-30
Completion
2014-04-30

Countries

  • China

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02147509 on ClinicalTrials.gov