Skip to main content
Clinical Trials/JPRN-UMIN000031215
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

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.

Registry
who.int
Start Date
March 1, 2018
End Date
TBD
Last Updated
2 years ago
Study Type
Interventional
Sex
All

Investigators

Sponsor
Aichi Medicak University Department of Ophthalmology

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

Similar Trials

Active, not recruiting
Not Applicable
Treatment of macular edema secondary to central or branch vein occlusion by dexamethazone intravitreal injection - Ozurdex in post-occlusive macular edemamacular edema seconday to central or branch retinal vein occlusionMedDRA version: 13.1Level: SOCClassification code 10015919Term: Eye disordersSystem Organ Class: 10015919 - Eye disorders
EUCTR2011-000425-72-ITIRCCS- FONDAZIONE G.B. BIETTI PER LO STUDIO E LA RICERCA IN OFTALMOLOGIA-ONLUS
Recruiting
Phase 4
Therapy of recalcitrant macular edema in aphakic and/or eyes with with severe iris-lens diaphragm disruption with longterm intravitreal steroid implants such as Iluvien® or Ozurdex®.recalcitrant macular edemaH35.8Other specified retinal disorders
DRKS00020282Augenklinik des Klnikums der Ludwig-Maximilians-Universität München40
Active, not recruiting
Phase 1
Treatment of macular edema due to central retinal vein occlusion with ranibizumab (Lucentis®). - Lucentis in CRVOThis case-series is designed to evaluate the safety and efficacy of intravitreal ranibizumab (Lucentis®) in the treatment of macular edema due to central retinal vein occlusion.MedDRA version: 12.1Level: LLTClassification code 10007972Term: Central retinal vein occlusionMedDRA version: 12.1Level: LLTClassification code 10054467Term: Macular edema
EUCTR2009-017782-30-ATMedizinische Universität Graz, Universitäts-Augenklinik
Completed
Phase 1
Treatment of macular edema secondary to central vein occlusiocentral vein occlusion.Other retinal vascular occlusions
IRCT201011295270N1Banco de Olhos de Sorocaba15
Active, not recruiting
Phase 1
Treatment of Cystoid Macular Edema following cataract surgery. A randomized, double-masked, placebo-controlled, clinical trial. - Treatment of post-cataract CME
EUCTR2009-017031-18-NLRotterdam Eye Hospital25