JPRN-UMIN000031215
Completed
未知
Treatment of macular edema secondary to branch retinal vein occlusion with sub-tenon triamcinolone acetonide injection - Treatment of macular edema following BRVO with STTA
Aichi Medicak University Department of Ophthalmology0 sites60 target enrollmentMarch 1, 2018
ConditionsMacular edema following BRVO
Overview
- Phase
- 未知
- Intervention
- Not specified
- Conditions
- Macular edema following BRVO
- Sponsor
- Aichi Medicak University Department of Ophthalmology
- Enrollment
- 60
- Status
- Completed
- Last Updated
- 2 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- Not provided
Exclusion Criteria
- •1\) The subject eye has retinal disease except BRVO. 2\) Transparency of the subject eye is turbid. 3\) Those who have active ocular infection or inactive toxoplasmosis. 4\) Those who have glaucoma or ocular hypertension, or medical histories of them. 5\) Those who have histories of herpetic infection in their subject eyes. 6\) Those who have uncontrollable systemic disease. 7\) Those who are systemic debility, or have severe heart disease, severe cerebral blood flow disorder or cirrhosis. 8\) Serum creatinine is 2\.0 mg/dL or more. 9\) Those who have undergone vitreous surgery to the subject eye or who are expected to undergo vitreous surgery. 10\) Those who have undertaken the following treatment within 24 weeks or who are expected to be undergone. Administration of corticosteroid to thesubject eye below the Tenon capsule or retro\-bulbar. Intravitreal of drug to the subject eye. Administration of immunosuppressant drug, immunomodulatory drug, antimetabolites drug and/or alkylating agents. Hyperbaric oxygen therapy or stellate ganglion block. Hemodialysis or peritoneal dialysis. 11\) Those who have received laser or intraocular surgery in the subject eye within 12 weeks or who are expected to undergo them. 12\) Those who have received treatments which are corticosteroid, oral carbonic anhydrase inhibitor, warfarin, heparin, heparin analogue, selective thrombin inhibitor, direct thrombin inhibitors or(/and) FXa inhibitors within 4 weeks. Those who are expected to undergo these therapies. 13\) Those who are planning of ophthalmic surgery during the observation period. 14\) Those who have drug allergy to the drugs which are used in this study. 15\) Those who cannot sufficient dilate pupil for inspection. 16\) Pregnant or lactating women.
Outcomes
Primary Outcomes
Not specified
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