All clinical trials on the European Union Clinical Trials Register (EUCTR) must report their results in the registry within a year of completion. This site tracks who's doing this and who isn't. Learn more »
These trials completed more than 12 months ago and should have reported results.
These trials are not yet due to report results: some are ongoing, some completed within the past 12 months.
These trials have problematic data on the registry. Details why »
Status | Trial ID | Title | Completion date | Category |
---|---|---|---|---|
Completed, but no date, and reported results | 2009-014409-15 | Prospective, randomized, multicenter, open label phase II study to access efficacy and safety of Lucentis monotherapy (ranibizumab 0.5 mg intravitreal injections) compared with Lucentis plus panretina... | bad-data | |
Completed, but no date | 2009-014612-34 | Prospective, multicenter, open-label study to evaluate the safety and efficacy of intravitreal ranibizumab in patients with subfoveal or juxtafoveal choroidal neovascularization (CNV) secondary to oth... | bad-data | |
Reported results | 2009-016760-36 | Prospective, randomized, open label phase II study to assess efficacy and safety of MacugenĀ® (pegaptanib 0.3 mg intravitreal injections) plus panretinal photocoagulation (PRP) and PRP (monotherapy) in... | 2012-10-31 | due-trials |
Reported results | 2013-003490-10 | Intraocular Pressure And Tolerability Study of Preservative Free Bimatoprost 0.03% Unit Dose (BUDPF) or preservative free Latanoprost 0.005% Unit Dose (LUDPF) (Monopost)in patients with Ocular hyperte... | 2015-02-17 | due-trials |
Reported results | 2013-003640-23 | Prospective, randomized, multicentre, open label, phase II / III study to assess efficacy and safety of ranibizumab 0.5 mg intravitreal injections plus panretinal photocoagulation (PRP) versus PRP in ... | 2016-05-27 | due-trials |
Reported results | 2014-003491-23 | A non-randomised, open-label, multicenter phase 4 pilot study on the effect and safety of IluvienĀ® in chronic diabetic macular edema patients considered insufficiently responsive to available therapie... | 2016-03-09 | due-trials |
Reported results | 2015-001368-20 | A Randomized, Double-masked, Sham-controlled Phase 4 Study of the Efficacy, Safety, and Tolerability of Intravitreal Aflibercept Monotherapy Compared to Aflibercept With Adjunctive Photodynamic Therap... | 2018-09-05 | due-trials |