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NCT02481167 Clinical Trial

Evaluation of Meibomian Gland Dysfunction in Chinese Old Patients

Dry Eye Clinical Trial

Clinical Trial Details — Status: Recruiting

Administrative data
NCT number NCT02481167
Other study ID # WZ-ZYY-DRYEYE
Secondary ID
Status Recruiting
Phase N/A
First received June 15, 2015
Last updated June 24, 2015
Start date January 2015
Est. completion date January 2018

Study information
Verified date June 2015
Source Wenzhou Medical University
Contact yinying zhao, PhD
Phone 86-057788068859
Email ginger146@126.com
Is FDA regulated No
Health authority China: Food and Drug Administration
Study type Observational

Clinical Trial Summary

The purpose of this study is to identify age-related changes in chinese meibomian glands that may be associated with meibomian gland dysfunction (MGD).

Recruitment information / eligibility
Status Recruiting
Enrollment 100
Est. completion date January 2018
Est. primary completion date April 2016
Accepts healthy volunteers No
Gender Both
Age group 40 Years to 80 Years
Eligibility Inclusion Criteria:

- have dry eye symptom

- have meibomian gland dysfunction

Exclusion Criteria:

- diabetes

- history of ocular surgery

- systemic disease or inflammation

Study Design

Observational Model: Cohort, Time Perspective: Cross-Sectional

Related Conditions & MeSH terms

Locations
Country Name City State
China Wenzhou Medical University Wenzhou Zhejiang

Sponsors (1)
Lead Sponsor Collaborator
Wenzhou Medical University

Country where clinical trial is conducted

China, 

Outcome
Type Measure Description Time frame Safety issue
Primary Tear film break-up time Tear film break-up time (TBUT) was evaluated by placing a single fluorescein strip over the inferior tear meniscus after instilling a drop of normal saline. 1 year Yes
Primary Lower tear meniscus Lower tear meniscus was evaluated by keratography 1 year Yes
Primary The morphology of meibomian glands The morphology of meibomian glands was evaluated by keratography 1 year Yes
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