Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-24 @ 6:41 PM
Ignite Modification Date:
2025-12-24 @ 6:41 PM
NCT ID:
NCT02399657
Eligibility Criteria:
Inclusion Criteria:
1. Patients diagnosed with CSME (clinically significant macular edema) with hard exudates within 1500 micrometer from foveal center
2. Those who have a BCVA (best corrected visual acuity) of study eye between 0.06(20/320) and 0.5(20/40)
3. Those who have a central macular thickness on OCT over 300 micrometer
4. If both eyes are eligible, eye having more hard exudates is selected (contralateral eye should be treated with corticosteroid other than Ozurdex or focal laser photocoagulation, anti-VEGF (vascular endothelial growth factor) injection is not allowed in contralateral eye)
Exclusion Criteria:
1. Those who have CSME without hard exudates
2. Those who have macular edema not related with diabetic retinopathy (e.g. AMD (age-related macular degeneration), uveitis, retinal vein occlusion and untreated malignant hypertension)
3. Those who have a history of Intraocular surgery (e.g. cataract surgery) within 3 months
4. Those who have a visual acuity of contralateral eye less than 0.1 (10/100)
5. Those who received focal laser treatment on macula within 3 months
6. Those who had intravitreal anti-VEGF agent injection within 3 months
7. Those who had intravitreal triamcinolone injection within 6 months
8. Those who have other ophthalmologic disease affecting visual acuity (e.g. central corneal opacity, cataract change at lens center)
9. Those who have severe systemic disease (e.g. uncontrolled DM, hypertension, cardiovascular disease, cerebrovascular disease)
10. Those who refuse to submit written consent
11. Those who cannot understand the contents of the clinical study and cooperate in the clinical trial
12. Those who are pregnant or lactating women
13. Those who have a history of vitrectomy
14. Those who require systemic corticosteroid or immunosuppressive agent treatment
15. Those who are banned from using Ozurdex
* Ocular infection or periocular infection
* Advanced glaucoma
* Hypersensitivity to dexamethasone or other component of Ozurdex
* Posterior lens capsule rupture or Aphakia
* Anterior chamber intraocular lens or posterior capsule rupture
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
20 Years
Maximum Age:
80 Years
Study:
NCT02399657
Study Brief:
Protocol Section:
NCT02399657