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Outcomes of Vitrectomy Combined With Subtenon Triamcinolone Injection for the Idiopathic Epiretinal Membrane

Y

Yeungnam University College of Medicine

Status

Unknown

Conditions

Epiretinal Membrane

Treatments

Procedure: Vitrectomy only group
Procedure: Combined therapy group

Study type

Interventional

Funder types

Other

Identifiers

NCT01630876
YUH-12-0309-M2

Details and patient eligibility

About

This study compares the anatomical and visual outcomes of patients with idiopathic epiretinal membrane(ERM) treated by vitrectomy and membrane peeling with or without subtenon triamcinolone acetonide injection

Enrollment

50 estimated patients

Sex

All

Ages

20 to 80 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • 1.The participant must have idiopathic epiretinal membrane 2.The participant must be willing and able to comply with the protocol.

Exclusion criteria

    1. The participant has idiopathic epiretinal membrane with other ocular vascular diseases such as Diabetes retinopathy, BRVO, etc.

    2. The participant has any additional ocular diseases that have irreversibly compromised or could likely compromise the visual acuity of the study eye including amblyopia, anterior ischemic optic neuropathy, clinically significant diabetic macular edema, severe non proliferative diabetic retinopathy, or proliferative diabetic retinopathy.

    3. The participant has had intraocular surgery (including lens replacement surgery).

    4. The participant has a history of (within the last six months), or current ocular or periocular infection (including any history of ocular herpes zoster or simplex).

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

50 participants in 2 patient groups

Vitrectomy only group
Sham Comparator group
Description:
The patients who will underwent 23- gauge transconjunctival sutureless vitrectomy only.
Treatment:
Procedure: Vitrectomy only group
Combined therapy group
Experimental group
Description:
The patients who will underwent 23- gauge transconjunctival sutureless vitrectomy with concomitant posterior subtenon Triamcinolone acetate injection.
Treatment:
Procedure: Combined therapy group

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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