- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02481167
Evaluation of Meibomian Gland Dysfunction in Chinese Old Patients
June 24, 2015 updated by: yin ying zhao, Wenzhou Medical University
The purpose of this study is to identify age-related changes in chinese meibomian glands that may be associated with meibomian gland dysfunction (MGD).
Study Overview
Status
Unknown
Conditions
Study Type
Observational
Enrollment (Anticipated)
100
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
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Zhejiang
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Wenzhou, Zhejiang, China, 325027
- Recruiting
- Wenzhou Medical University
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Contact:
- XIXIA DING, PHD
- Phone Number: 86-057788068859
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
40 years to 80 years (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Probability Sample
Study Population
This study was consisted of patients with older than 40 years of age who complained with dry eye.
The institutional review board of Wenzhou Medical College approved the study protocol, and all patients provided their informed consent.
Description
Inclusion Criteria:
- have dry eye symptom
- have meibomian gland dysfunction
Exclusion Criteria:
- diabetes
- history of ocular surgery
- systemic disease or inflammation
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
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group1
This study was consisted of patients with older than 40 years of age who complained with dry eye.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Tear film break-up time
Time Frame: 1 year
|
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.
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1 year
|
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Lower tear meniscus
Time Frame: 1 year
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Lower tear meniscus was evaluated by keratography
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1 year
|
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The morphology of meibomian glands
Time Frame: 1 year
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The morphology of meibomian glands was evaluated by keratography
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1 year
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Study Chair: ZHAO YUNE, MS, Wenzhou Medical University
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
General Publications
- Li J, Ma J, Hu M, Yu J, Zhao Y. Assessment of tear film lipid layer thickness in patients with Meibomian gland dysfunction at different ages. BMC Ophthalmol. 2020 Oct 6;20(1):394. doi: 10.1186/s12886-020-01667-8.
- Wu Y, Li J, Hu M, Zhao Y, Lin X, Chen Y, Li L, Zhao YE. Comparison of two intense pulsed light patterns for treating patients with meibomian gland dysfunction. Int Ophthalmol. 2020 Jul;40(7):1695-1705. doi: 10.1007/s10792-020-01337-0. Epub 2020 Mar 21.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
January 1, 2015
Primary Completion (Anticipated)
April 1, 2016
Study Completion (Anticipated)
January 1, 2018
Study Registration Dates
First Submitted
June 15, 2015
First Submitted That Met QC Criteria
June 24, 2015
First Posted (Estimate)
June 25, 2015
Study Record Updates
Last Update Posted (Estimate)
June 25, 2015
Last Update Submitted That Met QC Criteria
June 24, 2015
Last Verified
June 1, 2015
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- WZ-ZYY-DRYEYE
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.