- Trials with a EudraCT protocol (270)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (2)
270 result(s) found for: Diabetic retinopathy.
Displaying page 1 of 14.
| EudraCT Number: 2020-003865-20 | Sponsor Protocol Number: 21618 | Start Date*: 2021-03-02 | |||||||||||
| Sponsor Name:Bayer AG | |||||||||||||
| Full Title: A clinical trial collecting Data from routine ophthalmological examinations of patients who were randomized to either finerenone or placebo in the two Bayer-sponsored Phase 3 clinical trials FIDELI... | |||||||||||||
| Medical condition: Diabetic Retinopathy | |||||||||||||
|
|||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: BG (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2006-005315-10 | Sponsor Protocol Number: 2006-011 | Start Date*: 2006-09-05 | |||||||||||
| Sponsor Name:OSPEDALE SACRO CUORE-DON CALABRIA | |||||||||||||
| Full Title: Evaluation of safety and efficacy on visual acuity outcome of intravitreal somministration of Bevacizumab in patients with diabetic retinopathy | |||||||||||||
| Medical condition: Diabetic Retinopathy | |||||||||||||
|
|||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2015-003955-23 | Sponsor Protocol Number: DR2 | Start Date*: 2016-04-15 | |||||||||||
| Sponsor Name:Dept. of Ophthalmology, Rigshospitalet – Glostrup | |||||||||||||
| Full Title: Diabetic retinopathy: Effects of melatonin treatment on visual functions and circadian rhythm. | |||||||||||||
| Medical condition: Diabetic Retinopathy and Sleep disorder | |||||||||||||
|
|||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DK (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2017-000250-19 | Sponsor Protocol Number: CADODIAME | Start Date*: 2017-06-13 | |||||||||||
| Sponsor Name:Fundació Hospital Universitari Vall d'Hebron - Institut de Recersa (VHIR) | |||||||||||||
| Full Title: Effect of calcium dobesilate in early stages of diabetic retinopathy | |||||||||||||
| Medical condition: Diabetic retinopathy | |||||||||||||
|
|||||||||||||
| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2020-002333-15 | Sponsor Protocol Number: 20739 | Start Date*: 2021-01-15 | |||||||||||
| Sponsor Name:Bayer AG | |||||||||||||
| Full Title: A Phase 2 randomized, placebo-controlled, double-masked proof-of concept study to investigate the efficacy and safety of runcaciguat (BAY 1101042) in patients with moderately severe to severe non-p... | |||||||||||||
| Medical condition: - Non-proliferative diabetic retinopathy: early stage of a medical condition in which damage occurs to the retina due to diabetes mellitus (DM) - DM is characterized by too much sugar in the blood | |||||||||||||
|
|||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Prematurely Ended) PL (Completed) CZ (Completed) PT (Completed) NL (Completed) DK (Completed) HU (Prematurely Ended) IT (Prematurely Ended) SK (Completed) BG (Completed) LV (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2009-009909-25 | Sponsor Protocol Number: KTvsMM1/09 | Start Date*: 2009-05-05 | |||||||||||
| Sponsor Name:Johann Wolfgang Goethe-Universität Frankfurt | |||||||||||||
| Full Title: Evaluation of the efficacy and safety of a Macugen monotherapy versus Combined Therapies in the Treatment of Diabetic Retinopathy – a single centre, randomized, prospective Phase II trial | |||||||||||||
| Medical condition: Medical condition: moderate to severe non-proliferative retinopathy with diabetic cystoid macular edema. | |||||||||||||
|
|||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2008-005032-33 | Sponsor Protocol Number: 70242 | Start Date*: 2009-01-22 | |||||||||||
| Sponsor Name:Gedeon Richter Plc. | |||||||||||||
| Full Title: Single center, exploratoric, double-blind, placebo controlled study to investigate the efficacy and tolerability of vinpocetine in patients with non-proliferative diabetic retinopathy | |||||||||||||
| Medical condition: Patients with type 2 diabetes mellitus with mild or moderate or severe non-proliferative diabetic retinopathy (NPDR). | |||||||||||||
|
|||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: HU (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2016-002639-14 | Sponsor Protocol Number: VGFTe-OD-1411 | Start Date*: 2016-12-29 |
| Sponsor Name:Regeneron Pharmaceuticals, Inc. | ||
| Full Title: A Phase 3, Double-Masked, Randomized Study of the Efficacy and Safety of Intravitreal Aflibercept Injection in Patients with Moderately Severe to Severe Nonproliferative Diabetic Retinopathy | ||
| Medical condition: NonProliferative Diabetic Retinopathy | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: HU (Completed) DE (Completed) GB (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2011-003297-81 | Sponsor Protocol Number: PDRPOZU1 | Start Date*: 2011-09-12 | |||||||||||
| Sponsor Name:St Eriks Eye Hospital | |||||||||||||
| Full Title: A prospective, randomized study on intravitreal Ozurdex for preventing recurrent vitreous hemorrhage following pars plana vitrectomy for proliferative diabetic retinopathy | |||||||||||||
| Medical condition: Proliferative diabetic retinopathy | |||||||||||||
|
|||||||||||||
| Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: SE (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2014-001351-23 | Sponsor Protocol Number: EGT022-01 | Start Date*: 2017-08-15 | |||||||||||
| Sponsor Name:EyeGene, Inc | |||||||||||||
| Full Title: A phase IIa, randomized, placebo-controlled, double-blind, parallel study to investigate the efficacy of EG-Mirotin subcutaneously administered in multiple doses on diabetic macular edema in diabet... | |||||||||||||
| Medical condition: diabetic retinopathy patients having early diabetic macular edema (DME) | |||||||||||||
|
|||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: HU (Prematurely Ended) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2015-002415-15 | Sponsor Protocol Number: TG-MV-015 | Start Date*: 2016-02-17 | |||||||||||
| Sponsor Name:ThromboGenics NV | |||||||||||||
| Full Title: A PHASE 2, RANDOMISED, DOUBLE-MASKED, SHAM-CONTROLLED, MULTI-CENTRE STUDY TO EVALUATE THE EFFICACY AND SAFETY OF OCRIPLASMIN IN INDUCING TOTAL POSTERIOR VITREOUS DETACHMENT (PVD) IN SUBJECTS WITH N... | |||||||||||||
| Medical condition: Moderately severe to very severe non-proliferative diabetic retinopathy (NPDR) | |||||||||||||
|
|||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Prematurely Ended) GB (Completed) CZ (Completed) BE (Completed) HU (Completed) ES (Completed) FR (Completed) IT (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2016-002656-24 | Sponsor Protocol Number: CTSULENS1 | Start Date*: 2018-01-23 | ||||||||||||||||
| Sponsor Name:University of Oxford (Clinical Trials and Research Governance)) | ||||||||||||||||||
| Full Title: A randomised placebo-controlled clinical trial of fenofibrate to prevent progression of non-proliferative retinopathy in diabetes | ||||||||||||||||||
| Medical condition: Diabetic retinopathy and diabetic maculopathy | ||||||||||||||||||
|
||||||||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: GB (GB - no longer in EU/EEA) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2013-000031-27 | Sponsor Protocol Number: | Start Date*: 2013-03-20 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Sponsor Name:Moorfields Eye Hospital | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Full Title: Intravitreal Ranibizumab (Lucentis) Therapy in Patients with Diabetic Ischaemic Macular Oedema (DIME) | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Medical condition: Ischaemic Diabetic Macular Oedema | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
|
||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Trial protocol: GB (Prematurely Ended) | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Trial results: View results | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| EudraCT Number: 2011-003304-20 | Sponsor Protocol Number: OKHN1006 | Start Date*: 2012-07-02 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Sponsor Name:Moorfields Eye Hospital NHS Foundation Trust | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Full Title: Randomised Controlled Trial of Intravitreal therapy with Avastin compared to Observation in Patients with Diabetic Ischaemic Macular Oedema ‘The DIME study’ | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Medical condition: Ischaemic Diabetic Macular Oedema | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
|
||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Trial protocol: GB (Prematurely Ended) | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Trial results: View results | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| EudraCT Number: 2019-002067-10 | Sponsor Protocol Number: BP41321 | Start Date*: 2020-07-27 | |||||||||||
| Sponsor Name:F. Hoffmann-La Roche Ltd | |||||||||||||
| Full Title: A randomized, double-masked, 48-week parallel-group, placebo-controlled, proof-of-concept study to investigate the efficacy and safety of RG7774 in patients with Diabetes Mellitus Type 1 or Type 2 ... | |||||||||||||
| Medical condition: Diabetic retinopathy | |||||||||||||
|
|||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (GB - no longer in EU/EEA) SK (Completed) PL (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2005-006182-14 | Sponsor Protocol Number: | Start Date*: 2006-02-20 | |||||||||||
| Sponsor Name:UNIVERSITA DEGLI STUDI DI UDINE | |||||||||||||
| Full Title: Intravitreal Bevacizumab Avastin, Roche, United Kingdom for exudative maculopathies | |||||||||||||
| Medical condition: Exudative maculopathy associated with retinovascular disease | |||||||||||||
|
|||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2007-005601-22 | Sponsor Protocol Number: poc1doxy | Start Date*: 2008-03-27 | |||||||||||
| Sponsor Name: | |||||||||||||
| Full Title: Proof–of–concept study 1 (POC1): Evaluation of effect of doxycycline versus placebo on retinal function and posterior segment neovascularization in patients with severe non-proliferative or early ... | |||||||||||||
| Medical condition: Diabetic retinopathy | |||||||||||||
|
|||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DK (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2016-002971-91 | Sponsor Protocol Number: 1386-0012 | Start Date*: 2017-10-19 | |||||||||||
| Sponsor Name:Boehringer Ingelheim Norway KS | |||||||||||||
| Full Title: A randomized, double-masked, placebo-controlled exploratory study to evaluate safety, tolerability, pharmacodynamics and pharmacokinetics of orally administered BI 1467335 for 12 weeks with a 12... | |||||||||||||
| Medical condition: diabetic retinopathy | |||||||||||||
|
|||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: NO (Completed) GR (Completed) GB (Completed) ES (Completed) IT (Completed) PT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2012-001200-38 | Sponsor Protocol Number: 4C-2011-02 | Start Date*: 2012-09-07 | |||||||||||
| Sponsor Name:BCN Peptides S.A. | |||||||||||||
| Full Title: Neurodegeneration as an early event in the pathogenesis of Diabetic Retinopathy: A multicentric, prospective, phase II-III, randomized controlled trial to assess the efficacy of neuroprotective dru... | |||||||||||||
| Medical condition: Prevention of neurodegeneration which occurs in Diabetic Retinopathy | |||||||||||||
|
|||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) GB (Completed) PT (Completed) DK (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2010-022433-29 | Sponsor Protocol Number: LATANO-2 | Start Date*: 2010-10-13 |
| Sponsor Name:Aarhus University Hospital, Department of Ophthalmology | ||
| Full Title: Pharmacological intervention on diabetic retinopathy with PGF | ||
| Medical condition: Diabetic retinopathy | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: DK (Completed) | ||
| Trial results: View results | ||
Subscribe to this Search
To subscribe to the RSS feed for this search click here
.
This will provide an RSS feed for clinical trials matching your search that have been added or updated in the last 7 days.
To subscribe to the RSS feed for this search click here
.
This will provide an RSS feed for clinical trials matching your search that have been added or updated in the last 7 days.
| Download Options: | |
|---|---|
| Number of Trials to download: | |
| Download Content: | |
| Download Format: | |
| Note, where multi-state trials are shown in search results, selecting "Full Trial details" will download full information for each of the member states/countries involved in the trial. | |
Query did not match any studies.