- Trials with a EudraCT protocol (204)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (164)
204 result(s) found for: Conjunctivitis.
Displaying page 1 of 11.
EudraCT Number: 2017-002729-39 | Sponsor Protocol Number: C-07-40 | Start Date*: 2017-11-07 | |||||||||||
Sponsor Name:Alcon Research Ltd | |||||||||||||
Full Title: An Evaluation of the Safety and Efficacy of Moxifloxacin AF Ophthalmic Solution 0.5% for the Treatment of Bacterial Conjunctivitis in the USA | |||||||||||||
Medical condition: Bacterial conjunctivitis | |||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: Outside EU/EEA | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-002730-23 | Sponsor Protocol Number: C-04-38 | Start Date*: 2017-11-07 | |||||||||||
Sponsor Name:Alcon Research Ltd | |||||||||||||
Full Title: An Evaluation of the Safety and Efficacy of Moxifloxacin AF Ophthalmic Solution 0.5% for the Treatment of Bacterial Conjunctivitis in the USA | |||||||||||||
Medical condition: Bacterial conjunctivitis | |||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: Outside EU/EEA | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-002727-24 | Sponsor Protocol Number: C-10-051 | Start Date*: 2017-11-07 | |||||||||||
Sponsor Name:Alcon Research | |||||||||||||
Full Title: An Evaluation of the Safety and Efficacy of Moxifloxacin Ophthalmic Solution 0.5% Versus Ofloxacin Ophthalmic Solution 0.3% in the Treatment of Bacterial Conjunctivitis in Chinese Patients | |||||||||||||
Medical condition: bacterial conjunctivitis | |||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: Outside EU/EEA | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-005623-16 | Sponsor Protocol Number: OY122013 | Start Date*: 2014-03-20 | |||||||||||
Sponsor Name:Minna Honkila | |||||||||||||
Full Title: ANTIBIOTICS VERSUS PLACEBO FOR ACUTE BACTERIAL CONJUNCTIVITIS IN CHILDREN: A RANDOMISED DOUBLE-BLIND PLACEBO-CONTROLLED TRIAL | |||||||||||||
Medical condition: Acute conjunctivitis | |||||||||||||
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Population Age: Infants and toddlers, Children, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-003953-41 | Sponsor Protocol Number: C-09-50 | Start Date*: 2017-11-22 | |||||||||||
Sponsor Name:Alcon Research Ltd | |||||||||||||
Full Title: An Open-label, Long-term Study, with AL-4943A Ophthalmic Solution, 0.2% in Patients with Allergic Conjunctivitis | |||||||||||||
Medical condition: Allergic conjunctivitis | |||||||||||||
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Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: Outside EU/EEA | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-003841-39 | Sponsor Protocol Number: JPN-P-2010-1 | Start Date*: 2017-11-07 | |||||||||||
Sponsor Name:Alcon Research | |||||||||||||
Full Title: Clinical Evaluation of 0.1% Olopatadine Hydrochloride Ophthalmic Solution in Paediatric Patients | |||||||||||||
Medical condition: allergic conjunctivitis | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: Outside EU/EEA | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-000209-31 | Sponsor Protocol Number: LACTO2 | Start Date*: 2007-03-08 | |||||||||||
Sponsor Name:UNIVERSITA CAMPUS BIOMEDICO | |||||||||||||
Full Title: Efficacy of Lactobacillus Rhamnosus GG on preventing acute phases in patients affected by allergic conjunctivitis | |||||||||||||
Medical condition: allergic conjunctivitis | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-002728-26 | Sponsor Protocol Number: C-12-028 | Start Date*: 2017-11-07 | |||||||||||
Sponsor Name:Alcon Research | |||||||||||||
Full Title: A Multicenter, Randomized, Double-Masked, Vehicle-Controlled, Parallel-Group Study Evaluating the Safety of olopatadine hydrochloride (AL-4943A) Ophthalmic Solution 0.77% Administered Once Daily | |||||||||||||
Medical condition: asymptomatic allergic conjunctivitis | |||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: Outside EU/EEA | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-000480-41 | Sponsor Protocol Number: FARM6AS8AW | Start Date*: 2008-05-27 | |||||||||||
Sponsor Name:UNIVERSITA' CAMPUS BIOMEDICO | |||||||||||||
Full Title: Multicenter, randomised, double masked, controlled clinical trial on the safety and efficacy of Cyclosporine A eye drop treatment on patients with ocular cicatricial pemphigoid. | |||||||||||||
Medical condition: Ocular cicatricial pemphigoid (OCP) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-003460-35 | Sponsor Protocol Number: E03/05/PP-M | Start Date*: 2005-10-27 | |||||||||||
Sponsor Name:ALK-Abelló, S.A. | |||||||||||||
Full Title: Evaluación de los cambios inmunológicos tras la inmunoterapia subcutánea con un extracto de Phleum pratense | |||||||||||||
Medical condition: Rhinoconjunctivitis | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-005263-31 | Sponsor Protocol Number: LEVOKETO_02-2020 | Start Date*: 2021-06-02 | |||||||||||
Sponsor Name:NTC SRL | |||||||||||||
Full Title: Assessment of the effects and tolerability of RD03/2016 (Levofloxacin; Ketorolac Trometamol 0.5+0.5% w/v eye drops solution) for the treatment of bacterial conjunctivitis in adults: a multicentre, ... | |||||||||||||
Medical condition: Bacterial conjunctivitis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Prematurely Ended) IT (Completed) DE (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-001838-26 | Sponsor Protocol Number: THEA-LT0455-PIV-09/16 | Start Date*: 2017-07-26 | |||||||||||
Sponsor Name:THEA | |||||||||||||
Full Title: Comparison of NAABAK® efficacy versus FLUCON® in the treatment of moderate manifestations of allergic conjunctivitis to birch pollen in subjects exposed to birch in ALYATEC’s environmental exposure... | |||||||||||||
Medical condition: Subjects presenting moderate allergic conjunctivitis to birch pollen | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-004317-27 | Sponsor Protocol Number: EXC458-C001/C-12-010 | Start Date*: 2017-07-03 | |||||||||||
Sponsor Name:Alcon China Ophthalmic | |||||||||||||
Full Title: A Comparative Study of Olopatadine Hydrochloride Ophthalmic Solution 0.2% QD vs Olopatadine Hydrochloride Ophthalmic Solution 0.1% BID in the Treatment of Allergic Conjunctivitis in Chinese Subjects | |||||||||||||
Medical condition: Allergic conjunctivitis | |||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: Outside EU/EEA | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-003361-25 | Sponsor Protocol Number: SHP640-303 | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:Shire Human Genetic Therapies, Inc. | |||||||||||||
Full Title: A Phase 3, Multi-center, Randomized, Double-Masked Study to Evaluate the Clinical Efficacy and Safety of SHP640 (PVP-Iodine 0.6% and Dexamethasone 0.1%) Ophthalmic Suspension Compared to Placebo in... | |||||||||||||
Medical condition: Bacterial Conjunctivitis | |||||||||||||
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Population Age: Newborns, Infants and toddlers, Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) EE (Completed) HU (Completed) ES (Completed) PL (Completed) AT (Completed) FR (Completed) GB (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-004473-26 | Sponsor Protocol Number: LT0427-PII-01/07 | Start Date*: 2007-10-16 | |||||||||||
Sponsor Name:Laboratoires Théa | |||||||||||||
Full Title: Efficacy and safety of sodium cromolyn eye drops compared with placebo eye drops in patients with a history of allergic conjunctivitis using the Conjunctival Allergen Challenge model. | |||||||||||||
Medical condition: allergic conjunctivitis | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-002319-41 | Sponsor Protocol Number: HULP-VIR-2014-01 | Start Date*: 2015-05-11 | |||||||||||
Sponsor Name:Ana Boto de los Bueis | |||||||||||||
Full Title: Clinical and virologic assesment of two therapeutic options: antiviral Ganciclovir 0.15% ophthalmic gel and physiologic saline solution 0.9% used in patients with acute adenoviral conjuntivitis. | |||||||||||||
Medical condition: Acute adenoviral conjunctivitis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-002501-23 | Sponsor Protocol Number: V040.05 | Start Date*: 2005-12-12 | |||||||||||
Sponsor Name:Stallergenes S.A | |||||||||||||
Full Title: A randomised, double-blind, placebo-controlled, multi-national, multi-centre, phase III extension study to assess the long term efficacy, safety and carry-over effect of one dose of sublingual imm... | |||||||||||||
Medical condition: Grass Pollen Related Allergic Rhinoconjunctivitis | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) AT (Prematurely Ended) CZ (Completed) SK (Completed) ES (Completed) DK (Completed) IT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-005227-33 | Sponsor Protocol Number: PILIT_2013 | Start Date*: 2013-03-22 | ||||||||||||||||
Sponsor Name:Department of Respiratory Diseases, Aarhus University Hospital | ||||||||||||||||||
Full Title: Effect of Intralymphatic Immunotherapy on Basophil Response and Plasma Cell Kinetics in Allergic Patients | ||||||||||||||||||
Medical condition: allergic rhino-conjunctivitis | ||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: DK (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2005-004768-22 | Sponsor Protocol Number: C-05-30 | Start Date*: 2006-06-12 | |||||||||||
Sponsor Name:ALCON ITALIA | |||||||||||||
Full Title: Clinical study of the mast-cell stabilizing effects of the Olopatadine using the Conjunctival Allergen Challeenge model | |||||||||||||
Medical condition: subjects with a clinical history of seasonal allergic conjunctivitis, but asymptomatic and free of any topical or systemic medication at baseline | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-005681-39 | Sponsor Protocol Number: FAR-0201 | Start Date*: 2007-01-22 | |||||||||||
Sponsor Name:FARMIGEA | |||||||||||||
Full Title: A RANDOMIZED, DOUBLE-BLIND, MULTICENTER PARALLEL GROUP STUDY ON EFFICACY AND SAFETY OF KETOTIFEN FUMARATE 0.05 OPHTHALMIC SOLUTION VERSUS KETOTIFEN FUMARATE 0.025 | |||||||||||||
Medical condition: Patients with seasonal allergic conjunctivitis and history of ocular allergies for at least 2 years. | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
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