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Characterization of Signs and Symptoms of Participants With and Without Meibomian Gland Dysfunction

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01979887
Enrollment
75
Registered
2013-11-08
Start date
2013-11-30
Completion date
2014-07-31
Last updated
2014-08-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Meibomian Glands

Brief summary

This is an exploratory study to evaluate endpoints used to characterize participants with and without meibomian gland dysfunction (MGD) and will evaluate the correlation between signs and symptoms of MGD. No investigational drug will be administered in this study.

Interventions

PROCEDUREMeibum Expression

Meibum expression as per protocol. No investigational drug is administered in this study.

Sponsors

Allergan
Lead SponsorINDUSTRY

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
40 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

-Participants characterized as with or without Meibomian Gland Dysfunction.

Exclusion criteria

* Lid heating therapy, therapeutic gland expression, or meibomian gland probing within 12 months of enrollment * Contact lens use in the 30 days prior to enrollment * Lid hygiene within 48 hours prior to enrollment * Use of eye makeup within 8 hours of enrollment * Eyelash growth-stimulating products within 30 days prior to enrollment * Use of systemic vitamins and/or systemic supplements containing omega 3 fatty acids within 60 days of enrollment * Use of systemic anti-histamines within 30 days prior to enrollment.

Design outcomes

Primary

MeasureTime frame
Meibum Quality Score in the Study Eye as Assessed by the Investigator Using a 4-Point ScaleDay 22

Countries

United Kingdom, United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 10, 2026