- Trials with a EudraCT protocol (7)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
7 result(s) found for: Otitis externa.
Displaying page 1 of 1.
EudraCT Number: 2018-000641-39 | Sponsor Protocol Number: C-05-37 | Start Date*: 2018-04-05 | |||||||||||
Sponsor Name:Alcon Research Ltd | |||||||||||||
Full Title: Safety and Efficacy Evaluation of Topical Moxidex Otic Solution in the Treatment of Acute Otitis Externa (AOE) | |||||||||||||
Medical condition: Acute Otitis externa | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: Outside EU/EEA | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-006086-17 | Sponsor Protocol Number: 55005646 | Start Date*: 2012-07-10 | |||||||||||
Sponsor Name:Maria Fernanda Pedrero Escalas | |||||||||||||
Full Title: "Effectiveness of homeopathic treatment (Agraphis nutans 5CH, Thuya occidentalis 5CH, Kalium muriaticum and Arsenicum iodatum 9CH 9CH) as adjuvant secretory otitis in children" | |||||||||||||
Medical condition: Pediatric patients aged 2 months to 12 years presenting secretory otitis | |||||||||||||
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Population Age: Infants and toddlers, Children, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-004441-42 | Sponsor Protocol Number: UK-06-RG-63 | Start Date*: 2007-03-01 | |||||||||||
Sponsor Name:Southport and Ormskirk Hospital NHS Trust | |||||||||||||
Full Title: A study to evaluate the role of tacrolimus ointment (Protopic®) 0.1% in the treatment of chronic otitis externa. | |||||||||||||
Medical condition: Chronic Otitis Externa | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-003463-22 | Sponsor Protocol Number: CLOTOT3-16IA03 | Start Date*: 2020-04-29 | |||||||||||
Sponsor Name:Laboratorios Salvat, S.A. | |||||||||||||
Full Title: A Phase III, Multicenter, Randomized, Double-Blind Clinical Trial to Assess the Efficacy and Safety of Clotrimazole 1% Otic Solution Compared to Placebo for the Treatment of Fungal Otitis Externa (... | |||||||||||||
Medical condition: Fungal Otitis Externa (Otomycosis) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) PT (Completed) BG (Completed) RO (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-000615-25 | Sponsor Protocol Number: C-07-13 | Start Date*: 2018-04-05 | |||||||||||
Sponsor Name:Alcon Research Ltd | |||||||||||||
Full Title: Safety and Efficacy Evaluation of Topical Moxidex Otic Solution in the Treatment of Acute Otitis Externa | |||||||||||||
Medical condition: Acute Otitis Externa | |||||||||||||
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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: 2005-001179-36 | Sponsor Protocol Number: C-04-72 | Start Date*: 2005-08-23 |
Sponsor Name:Alcon Pharma GmbH | ||
Full Title: Efficacy and safety of Dexa-Polyspectran® drops, preserved with benzalkonium chloride, vs. Dexa-Polyspectran® drops without dexamethasone phosphate, preserved with benzalkonium chloride, in patient... | ||
Medical condition: acute bacterial otitis externa | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2005-001180-65 | Sponsor Protocol Number: C-04-73 | Start Date*: 2005-08-22 |
Sponsor Name:Alcon Pharma GmbH | ||
Full Title: Efficacy and safety of Polyspectran® drops, preserved with benzalkonium chloride vs. glycerol ear drops in patients with acute bacterial otitis externa – A double-blind, multicenter, prospective, ... | ||
Medical condition: acute bacterial otitis externa | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: View results |
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