<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>16</volume><submitter>Nawar AE</submitter><pubmed_abstract>&lt;h4>Purpose&lt;/h4>The present study evaluated the efficacy of combined suprachoroidal injection of triamcinolone acetonide (TA) using a modified microneedle with intravitreal injection of ranibizumab in branch retinal vein occlusion (BRVO) patients.&lt;h4>Patients and methods&lt;/h4>This is a prospective randomised interventional study that was conducted on 60 eyes of 60 patients with non ischemic BRVO. Patients were divided in two groups, group (1) 30 patients who received intravitreal injection of 0.05 mL (0.5 mg) of ranibizumab, group (2) included 30 patients who received baseline combined intravitreal injection of 0.05 mL (0.5 mg) of ranibizumab and suprachoroidal injection of triamcinolone acetonide (4mg/0.1mL), both groups received monthly injection of ranibizumab on pro-re-nata (PRN) regime</pubmed_abstract><journal>Clinical ophthalmology (Auckland, N.Z.)</journal><pagination>1139-1151</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9034893</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Modified Microneedle for Suprachoroidal Injection of Triamcinolone Acetonide Combined with Intravitreal Injection of Ranibizumab in Branch Retinal Vein Occlusion Patients.</pubmed_title><pmcid>PMC9034893</pmcid><pubmed_authors>Nawar AE</pubmed_authors></additional><is_claimable>false</is_claimable><name>Modified Microneedle for Suprachoroidal Injection of Triamcinolone Acetonide Combined with Intravitreal Injection of Ranibizumab in Branch Retinal Vein Occlusion Patients.</name><description>&lt;h4>Purpose&lt;/h4>The present study evaluated the efficacy of combined suprachoroidal injection of triamcinolone acetonide (TA) using a modified microneedle with intravitreal injection of ranibizumab in branch retinal vein occlusion (BRVO) patients.&lt;h4>Patients and methods&lt;/h4>This is a prospective randomised interventional study that was conducted on 60 eyes of 60 patients with non ischemic BRVO. Patients were divided in two groups, group (1) 30 patients who received intravitreal injection of 0.05 mL (0.5 mg) of ranibizumab, group (2) included 30 patients who received baseline combined intravitreal injection of 0.05 mL (0.5 mg) of ranibizumab and suprachoroidal injection of triamcinolone acetonide (4mg/0.1mL), both groups received monthly injection of ranibizumab on pro-re-nata (PRN) regime</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022</publication><modification>2025-04-20T00:17:19.384Z</modification><creation>2025-02-19T01:53:36.845Z</creation></dates><accession>S-EPMC9034893</accession><cross_references><pubmed>35469288</pubmed><doi>10.2147/OPTH.S361636</doi></cross_references></HashMap>