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A prospective study on the prognosis of idiopathic epimacular membrane after vitrectomy

A prospective study on the prognosis of idiopathic epimacular membrane after vitrectomy

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100044228
Enrollment
Unknown
Registered
2021-03-12
Start date
2021-03-11
Completion date
Unknown
Last updated
2021-08-30

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

Conditions

Idiopathic epimacular membrane

Interventions

experimental group:intravitreal injection of ozurdex
control group:Nil

Sponsors

Tianjin Medical University Eye Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Aged >= 40 years; 2. The diagnosis of idiopathic epimacular membrane requires vitrectomy combined with membrane peeling; 3. There was no injection of anti angiogenic factor drugs within 3 months before or after operation; 4. At least part of the cornea is transparent (or the central area of the cornea is transparent), which can ensure the fundus examination, visual function examination and OCT examination after vitrectomy.

Exclusion criteria

Exclusion criteria: 1. Have participated in other clinical trials within 4 weeks before the start of this study, or have received intrabulbar injection of this drug or other drugs within 3 months before the start of this study; 2. Known adverse reactions to ozurdex or triamcinolone acetonide (TA); 3. Glaucoma with high intraocular pressure or definite diagnosis (including steroid glaucoma); 4. Previously had proliferative diabetic retinopathy, retinal vascular disease, and proliferative vitreoretinopathy; 5. Suspected or confirmed infectious lesions around the eyes (herpes simplex virus, varicella zoster virus, bacterial infection, fungal infection, etc.); 6. Patients with previous congenital eye abnormalities, ocular trauma, and eye diseases seriously affecting vision; 7. Pregnant or lactating women; 8. Patients with mental history.

Design outcomes

Primary

MeasureTime frame
vision;central macular thickness;

Secondary

MeasureTime frame
Intraocular pressure;Multifocal electrophysiology;microperimetry;octa;

Countries

China

Contacts

Public ContactShao Yan

Tianjin Medical University Eye Hospital

sytmueh@163.com+86 17622651170

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 8, 2026