Skip to content

The therapeutic evaluation of E-Eye on meibomian gland dysfunction patient

The therapeutic evaluation of Intense Regulation Pulse Light on meibomian gland dysfunction patient

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR-ONB-17014021
Enrollment
Unknown
Registered
2017-12-18
Start date
2017-12-18
Completion date
Unknown
Last updated
2018-01-29

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

Conditions

meibomian gland dysfunction

Interventions

treatment group:IRPL treatment

Sponsors

Tianjin Medical University Eye Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Aged greater than or equal to 18 years old male and female; 2. The subject signed the informed consent; 3. Main complaint eye dry, eye astringent, visual fatigue and other eye symptoms; 4. Diagnosis of MGD; 5. SPEED score is greater than or equal to 6 points; 6. MGYSS is less than or equal to 12 points; 7. Skin type meets the standard.

Exclusion criteria

Exclusion criteria: 1. Patients with discomfort or adverse reactions to the treatment; 2. 6 months with ocular trauma history and surgical history; 3. Patients with eye inflammation, allergies and other eye diseases; 4. Patients with abnormal eyelids; 5. Within 5.3 months, contact lens wear history; 6. A history of tanning and sunburn within 6.4 weeks; 7. Effects of systemic disease on the eyes or medications that affect the eye table; 8. Patients with lacrimal duct or lacrimal embolism; 9. Treatment area has skin disease or abnormality; 10. The overall condition was poor, and the researchers considered that it was impossible to evaluate the efficacy or to complete the expected course of treatment and follow-up; 11. Disuse eye drops or other treatments other than artificial tears for the first two weeks; 12. Pregnant and lactating women; 13. The clinical researchers judged that the other patients should not be included.

Design outcomes

Primary

MeasureTime frame
lipid layer thickness;tear break up time;tear inflammatory factor;

Countries

China

Contacts

Public ContactShaozhen Zhao

Tianjin Medical University Eye Hospital

zhaosz1997@sina.com+86 13802036813

Outcome results

None listed

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