- Trials with a EudraCT protocol (74)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
74 result(s) found for: Ear infections.
Displaying page 1 of 4.
EudraCT Number: 2017-000820-83 | Sponsor Protocol Number: NNL-2017 | Start Date*: 2017-07-03 | ||||||||||||||||
Sponsor Name:University of Oulu | ||||||||||||||||||
Full Title: Otitis Media and Nasopharyngeal Microbiome in Children. The change of nasopharyngeal microbiome and its role as a risk factor of otitis media. Streptococcus salivarius K12 and the change of nasop... | ||||||||||||||||||
Medical condition: We investigate role of microbiota as the risk factor of acute otitis media in children. | ||||||||||||||||||
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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: 2012-000341-13 | Sponsor Protocol Number: OTV.PRE.01 | Start Date*: 2012-08-28 | ||||||||||||||||
Sponsor Name:Weber & Weber GmbH & Co. KG | ||||||||||||||||||
Full Title: Efficacy and Safety of an Herbal-Based Medication vs. Placebo in Preventing Acute Otitis Media in Children at High Risk of Recurrence: A Placebo Controlled, Randomized, Double-blinded Parallel-Grou... | ||||||||||||||||||
Medical condition: recurrent acute otitis media | ||||||||||||||||||
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Population Age: Infants and toddlers, Children, Under 18 | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Completed) | ||||||||||||||||||
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: 2018-000643-37 | Sponsor Protocol Number: C-09-033 | 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 Media with Otorrhea in Tympanostomy Tubes | |||||||||||||
Medical condition: Acute Otitis Media | |||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: Outside EU/EEA | |||||||||||||
Trial results: View results |
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: 2020-001076-14 | Sponsor Protocol Number: K12-2020 | Start Date*: 2020-04-20 | |||||||||||
Sponsor Name:Oulu University Hospital, Oulu, Finland [...] | |||||||||||||
Full Title: Efficacy of Streptococcus salivarius K12 oral probiotic products in preventing acute otitis media: A randomized placebo-controlled trial. | |||||||||||||
Medical condition: Acute otitis media | |||||||||||||
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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: 2010-023991-15 | Sponsor Protocol Number: KB042 | Start Date*: 2011-03-10 | |||||||||||
Sponsor Name:KEDRION | |||||||||||||
Full Title: Efficay and Safety Evaluation of Kedrion Fibrin Sealant, in middle ear microsurgery. Monocenter, controlled, single blind, randomised, two parallel arms, phase II/III study | |||||||||||||
Medical condition: Chronic otitis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-002689-30 | Sponsor Protocol Number: C-13-026 | Start Date*: 2017-11-20 | |||||||||||
Sponsor Name:Alcon Research Ltd | |||||||||||||
Full Title: Proof-of-Concept Study of a Single Application of an Investigational Otic Suspension in Treatment of Acute Otitis Media With Tympanostomy Tubes | |||||||||||||
Medical condition: Acute otitis media | |||||||||||||
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Population Age: Infants and toddlers, Children, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: Outside EU/EEA | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-000640-26 | Sponsor Protocol Number: C-05-36 | Start Date*: 2018-04-05 | |||||||||||
Sponsor Name:Alcon Research Ltd | |||||||||||||
Full Title: Safety and Efficacy Evaluation of Topical Moxidex Otic Solution Compared to Moxifloxacin Solution in the Treatment of Acute Otitis Media with Otorrhea through Tympanostomy Tubes (AOMT) | |||||||||||||
Medical condition: acute otitis media | |||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: Outside EU/EEA | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-023239-40 | Sponsor Protocol Number: CIFLOTIII/10IA04 | Start Date*: 2011-07-27 | |||||||||||
Sponsor Name:Laboratorios SALVAT, S.A. | |||||||||||||
Full Title: A Multicenter, Randomized, Double-Blind Clinical Trial to Assess the Efficacy and Safety of Ciprofloxacin 0.3% plus Fluocinolone Acetonide 0.025% Otic Solution Compared to Ciprofloxacin 0.3% Otic s... | |||||||||||||
Medical condition: Acute Otitis Media with Tympanostomy Tubes (AOMT) in Pediatric Patients | |||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) SE (Completed) FI (Completed) DK (Completed) CZ (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-023238-22 | Sponsor Protocol Number: CIFLOTIII/10IA02 | Start Date*: 2011-07-29 | |||||||||||
Sponsor Name:Laboratorios SALVAT, S.A. | |||||||||||||
Full Title: A Multicenter, Randomized, Double-Blind Clinical Trial to Assess the Efficacy and Safety of Ciprofloxacin 0.3% plus Fluocinolone Acetonide 0.025% Otic Solution Compared to Ciprofloxacin 0.3% Otic s... | |||||||||||||
Medical condition: Acute Otitis Media with Tympanostomy Tubes (AOMT) in Pediatric Patients. Otitis Media Aguda con Tubos de TimpanostomĂa(AOMT) en Pacientes Pediatricos | |||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) SE (Completed) FI (Completed) DK (Completed) CZ (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-000132-40 | Sponsor Protocol Number: AM-111-CL-08-01 | Start Date*: 2008-11-18 | |||||||||||
Sponsor Name:Auris Medical AG | |||||||||||||
Full Title: Efficacy of AM 111 in Patients with Acute Sensorineural Hearing Loss: A Multi-Centre, Double-Blind, Randomised, Placebo-Controlled, Dose-Escalation Phase II Study | |||||||||||||
Medical condition: Acute sensorineural hearing loss (ASNHL), which may be triggered by acoustic trauma, middle or inner ear surgery, i.e. known or evident insults to the inner ear. ASNHL may also result from a variet... | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) CZ (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-000642-19 | Sponsor Protocol Number: C-05-38 | 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 Peri-Operative Tube Otorrhea | |||||||||||||
Medical condition: Acute Otitis Media | |||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: Outside EU/EEA | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-004637-47 | Sponsor Protocol Number: EFC6132,HMR3647B/3002 | Start Date*: 2015-03-17 | |||||||||||
Sponsor Name:Sanofi-aventis | |||||||||||||
Full Title: Multinational, Randomized, Double-Blind, Double-Dummy, Comparative Study to Evaluate the Efficacy and Safety of 5 Days Telithromycin 25mg/kg od Versus 5 Days Azithromycin 10 mg/kg od Followed by 5 ... | |||||||||||||
Medical condition: Otitis Media, Suppurative Otitis Media, Purulent | |||||||||||||
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Population Age: Infants and toddlers, Children, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: Outside EU/EEA | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-004077-32 | Sponsor Protocol Number: BCRU/11/Ibu-AOM/001 | Start Date*: 2015-12-29 |
Sponsor Name:Berlin-Chemie AG | ||
Full Title: A randomized open-label, multinational, multicentre, phase III clinical study to evaluate the efficacy and safety of Ibuprofen oral suspension 20 mg/ml and Ibuprofen oral suspension 40 mg/ml (Berli... | ||
Medical condition: Acute otitis media (AOM) is an acute inflammatory disease involving the mucosa of the middle ear. AOM is one of the most frequent complications of upper respiratory tract infections in children. T... | ||
Disease: | ||
Population Age: Children, Under 18 | Gender: Male, Female | |
Trial protocol: Outside EU/EEA | ||
Trial results: View results |
EudraCT Number: 2011-005187-25 | Sponsor Protocol Number: BUC-SI-11-001 | Start Date*: 2012-05-31 | |||||||||||
Sponsor Name:SOCIETA' LABORATORIO FARMACEUTICO S.I.T. SRL | |||||||||||||
Full Title: Efficacy and tolerability clinical trial of an immunostimulant made from inactivated bacteria (BUCCALIN) in the prophylaxis of infection of the airways (rhinotracheobronchitis, colds). Double-blind... | |||||||||||||
Medical condition: Episodes classified by upper respiratory infections (otitis, tonsillitis, sinusitis, pharyngotonsillitis, nasopharyngitis) and lower respiratory tract (bronchitis, pneumonia). | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
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: 2011-002140-27 | Sponsor Protocol Number: 112909 | Start Date*: 2012-04-12 | ||||||||||||||||
Sponsor Name:GlaxoSmithKline Biologicals | ||||||||||||||||||
Full Title: A phase III, open study in children previously enrolled in study 10PN-PD-DIT-037 (111188) to assess the immunogenicity, safety and reactogenicity of GlaxoSmithKline (GSK) Biologicals’ 10-valent pne... | ||||||||||||||||||
Medical condition: Healthy volunteers (Vaccination against Streptococcus pneumoniae in healthy children previously enrolled in study 10PN-PD-DIT-037 (111188).) | ||||||||||||||||||
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Population Age: Infants and toddlers, Under 18 | Gender: Male, Female | |||||||||||||||||
Trial protocol: Outside EU/EEA | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2016-002927-27 | Sponsor Protocol Number: OY20167 | Start Date*: 2016-08-15 |
Sponsor Name:University of Oulu, Department of Pediatrics, PEDEGO-Research unit | ||
Full Title: Effect of antimicrobial treament of acute otitis media on the intestinal micobiome in children: A randomized controlled trial | ||
Medical condition: | ||
Disease: | ||
Population Age: Infants and toddlers, Children, Under 18 | Gender: Male, Female | |
Trial protocol: FI (Completed) | ||
Trial results: View results |
EudraCT Number: 2016-003927-45 | Sponsor Protocol Number: SENS-111-201 | Start Date*: 2017-05-04 | |||||||||||
Sponsor Name:Sensorion SA | |||||||||||||
Full Title: A multicentre, randomized, double-blind, placebo-controlled study to assess the efficacy and safety of 2 dose regimens of orally administered SENS-111 (100mg and 200mg) given during 4 days in patie... | |||||||||||||
Medical condition: Acute Unilateral Vestibulopathy | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) CZ (Completed) HU (Completed) ES (Prematurely Ended) PL (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
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