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Effect of Sunflower Lecithin Supplementation on Meibomian Gland Function in Adults With Dry Eye Disease

Effect of Sunflower Lecithin Supplementation on Meibomian Gland Function in Adults With Dry Eye Disease

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06058559
Enrollment
31
Registered
2023-09-28
Start date
2023-06-20
Completion date
2023-10-26
Last updated
2024-03-15

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

Conditions

Dry Eye Disease, Meibomian Gland Dysfunction

Brief summary

This prospective study will evaluate the effect of oral sunflower lecithin dietary supplementation on meibomian gland function in adults with dry eye disease.

Detailed description

Enrolled patients in the active arm of the study (n=20) will receive a daily dose of four sunflower lecithin 1,200 mg soft-gel capsules for a duration of 90 days. Patients in the control arm (n=10) will receive four doses of a 1,000 mg placebo soft-gel capsules (containing olive oil). Patients will be evaluated for meibomian gland function and signs and symptoms of dry eye at baseline and at the end of the study using a standardized eye dryness survey (SPEED survey), Tear Breakup Time Measurement, Meibomian Gland Score, and a rapid in-office assessment of years (InflammaDry).

Interventions

DIETARY_SUPPLEMENTSunflower lecithin

Lecithins are a group of essential phospholipids that are involved in a number of biological functions such as lipid-cholesterol transport, transmembrane signaling, and neurological function

DIETARY_SUPPLEMENTOlive oil

Extra virgin olive oil

Sponsors

Virginia Lions Institute Foundation
CollaboratorUNKNOWN
George Washington University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
DOUBLE (Subject, Investigator)

Masking description

Double (Participant, Investigator)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Age greater than18 at the time of informed consent * Clinical diagnosis of dry eye in both eyes * Fluorescein tear film break-up time (TBUT) less than 10s in both eyes * The presence of lid margin scaling, telangiectasia, collarette or meibomian gland plugging on slit-lamp examination * Best-corrected visual acuity (BCVA, Snellen) of 20/40 or better in each eye * Patient Evaluation of Eye Dryness (SPEED) questionnaire score \>6 to \<14 * Must understand; be willing and able, and likely to fully comply with study procedures, visit schedule, and restrictions

Exclusion criteria

* Any pre-existing ocular disease other than dry eye disease * Patients with inability to swallow soft gel capsules * Severe illness, pregnancy or breastfeeding, smoking, and regular use of strongly anticholinergic drugs. * Drastic change of food and/or food supplements within the last month. * Other food supplement with fatty acids * Evidence of acute ocular infection and⁄or intraocular inflammation within 1 month prior to the onset of this study. * Ocular surgery within the last 6 months. * Patients treated with topical ocular, steroidal or non-steroidal, anti-inflammatory treatment within the last month. * Occlusion therapy with lacrimal or punctum plugs within the last 3 months. * Alterations of the lacrimal drainage system * Eyelid abnormalities * Patients on oral tetracycline or corticosteroids * Active allergy or infection at the ocular surface

Design outcomes

Primary

MeasureTime frameDescription
Change from Baseline of the SPEED questionnaire score at Day 9090 daysTo assess the improvement of dry eye symptoms by SPEED questionnaire. 0 score is the minimum (no dry eye symptom); 64 is the maximum score (most symptomatic). Change = (Day 90 score - Baseline score)

Secondary

MeasureTime frameDescription
Change from Baseline of Fluorescein Tear Break-Up Time (Seconds) at Day 9090 daysFluorescein Tear Break-Up Time (TBUT) is a measurement in seconds of tear film stability. The shorter the TBUT, the lower the tear film stability. Lower tear film stability is associated with dry eye. Change = (Day 90 value - Baseline value)
Change in number of MMP-positive eyes at Day 9090 daysInflammaDry is a noninvasive immunoassay for detecting the presence of MMP-9 in tears.
Least Squares Mean Change from Baseline in Meibomian Gland Score (MGS) at Day 9090 daysMeibomian glands on the eyelids assessed by the examiner using a Meibomian Gland Evaluator (MGE) and a slit lamp microscope. An MGE instrument applies a standardized force simulating the pressure of a deliberate blink allowing eye care professionals to observe meibomian gland functionality through a slit lamp. 5 glands in 1 zone (nasal) evaluated for each eye and scored from 0 to 3, with a resultant overall score (MGS) of 0 to 15 for each eye. Scoring as follows: 0 = no secretion (worst), 1 = inspissated, 2 = cloudy, 3 = clear liquid (best). A higher change from baseline score indicates an improvement in meibomian gland function.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026