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Efficacy and tolerability of 0.2% hyaluronic acid and 2% ectoin topical eye drops, Vitamin A ointment, and lid wipe in post-COVID Meibomian Gland Dysfunction (MGD): a 3-arm randomized clinical trial

Efficacy and tolerability of 0.2% hyaluronic acid and 2% ectoin topical eye drops, Vitamin A ointment, and lid wipe in post-COVID Meibomian Gland Dysfunction (MGD): a 3-arm randomized clinical trial

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300067758
Enrollment
Unknown
Registered
2023-01-20
Start date
2023-02-01
Completion date
Unknown
Last updated
2023-05-15

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

Conditions

Meibomian gland dysfunction

Interventions

Group A:Topical 0.2% hyaluronic acid + 2% ectoin eye drops (Hylo Dual Intense, HI)
Group B:HI eye drops and nocturnal Vitamin A ointment (Hylo Night, HN)
Group C:HI eye drops and nocturnal HN ointment plus Optiben (OB) lid wipe

Sponsors

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

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Post-COVID infection patients; 2. Ocular surface disease index (OSDI) >= 13; 3. Non-invasive tear break up time = grade 2 in one eyelid; 5. >= 18 years of age with no upper age limit; 6. Agree to attend follow-up visits and comply to treatment regimen.

Exclusion criteria

Exclusion criteria: 1. Patients with drug allergy history or allergic constitution; 2. Allergy to lid wipe; 3. Contact lens wear 3 months before or during the study period; 4. Use of topical (including anti-glaucomatous, cyclosporin, antibiotics) or systemic medication known to affect (worsen or improve) MGD 3 months before or during the study period; 5. Major systemic (e.g. Sjogrens syndrome), dermatologic (e.g. Rosacea) known to affect MGD or ocular conditions (including thyroid eye disease, recurrent conjunctivitis, ocular allergies); 6. Ocular procedures (excluding uncomplicated cataract operation) 3 months before and any ocular procedure during the study period; 7. Women who are pregnant, nursing, planning pregnancy, or of childbearing potential not using a reliable method of contraception.

Design outcomes

Primary

MeasureTime frame
Change from baseline Tear film breakup time (TFBUT);

Countries

China

Contacts

Public ContactDr Chong Kam Lung Kelvin

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

chongkamlung@cuhk.edu.hk+852 39435805

Outcome results

None listed

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