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Metabolomics study in meibomian gland dysfunction

Metabolomics study in meibomian gland dysfunction

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600121279
Enrollment
Unknown
Registered
2026-03-27
Start date
2026-04-01
Completion date
Unknown
Last updated
2026-03-30

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

Conditions

Meibomian gland dysfunction

Interventions

Meibomian gland dysfunction group :None

Sponsors

Department of Ophthalmology and Visual Sciences (DOVS), Chinese University of Hong Kong
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1.MGD patients: (1) >=18 years of age with no upper age limit; (2) Provide informed consent; (3) Newly diagnosed with MGD within the last twelve months; (4) Symptomatic dry eye ocular surface disease index (OSDI) = 13; (5) Mild to moderate (level 3-4) MGD on at least one eye; (6) Ethnic Chinese 2.Control Group: (1) >=18 years of age with no upper age limit; (2) Provide informed consent; (3) Symptomatic dry eye ocular surface disease index (OSDI) < 13; (4) Mild to moderate (level 0-2) MGD on both eyes; (5) Ethnic Chinese

Exclusion criteria

Exclusion criteria: MGD patients and the control group: (1) Contact lens wear 3 months before or during the study period; (2) Use of topical (including anti-glaucomatous, cyclosporin, antibiotics, steroid) or systemic medication known to affect (worsen or improve) MGD 3 months before or during the study period; (3) Major systemic (e.g. Sjogren’s syndrome), dermatologic (e.g. Rosacea) known to affect MGD or ocular conditions (including thyroid eye disease, recurrent conjunctivitis, ocular allergies); (4) Ocular procedures (excluding uncomplicated cataract operation) 3 months before and any ocular procedure during the study period; (5) Dermatological treatment [including chemical peeling, laser, intense pulsed light (IPL) or energy device in the periocular and facial region] 6 months before or during the study period; (6) Contraindications to IPL therapy (including recent sun-burn, photosensitivity, active or pigmented skin lesions, cancer, implants, tattoos, semi-permanent makeup in the periocular area; (7) Women who are pregnant, nursing, planning pregnancy, or of childbearing potential not using a reliable method of contraception; (8) Tear breakup time (TFBUT)>10 seconds in both eyes; (9) Presence of eyelid pathologies and malposition including eyelid swelling, dermatochalasis, entropion, ectropion, lash ptosis and lagophthalmos.

Design outcomes

Primary

MeasureTime frame
The ophthalmopathy status of the MGD patients and healthy subjects;The meibum metabolomics in local Hong Kong MGD patients;

Secondary

MeasureTime frame
The correlations of metabolites with meibomian gland and ocular surface parameter;

Countries

China

Contacts

Public ContactCHU Wai Kit

Department of Ophthalmology and Visual Sciences, The Chinese University of Hong Kong

waikit@cuhk.edu.hk+852 3943 5860

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Apr 4, 2026