- Trials with a EudraCT protocol (371)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (1,733)
371 result(s) found for: Ear.
Displaying page 4 of 19.
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: 2015-002375-22 | Sponsor Protocol Number: 38RC15.173 | Start Date*: 2015-07-27 | |||||||||||
Sponsor Name:University Hospital Grenoble | |||||||||||||
Full Title: Study the diffusion kinetics of gadolinium at the perilymph of the inner ear structures to patients Meniere's disease | |||||||||||||
Medical condition: Patients Meniere's disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-004323-33 | Sponsor Protocol Number: AC102-201 | Start Date*: 2022-05-06 |
Sponsor Name:AudioCure Pharma GmbH | ||
Full Title: Phase II, Multi-Center, Randomized, Blinded Study Evaluating the Efficacy, Safety and Tolerability of a Single Intratympanic Dose of AC102 Compared to Oral Steroids for the Treatment of Idiopathic ... | ||
Medical condition: Idiopathic Sudden Sensorineural Hearing Loss (ISSNHL) ISSNHL is most commonly defined as sensorineural hearing loss of 30dB or greater over at least three contiguous audiometric frequencies occurri... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Trial now transitioned) CZ (Trial now transitioned) BG (Prematurely Ended) AT (Trial now transitioned) NL (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2015-003929-34 | Sponsor Protocol Number: AUT042063 | Start Date*: 2016-03-10 | |||||||||||
Sponsor Name:Autifony Therapeutics Limited | |||||||||||||
Full Title: A Pilot Double-blind, Placebo-controlled Crossover Study to Explore the Possible Benefit of AUT00063, an Oral Modulator of Voltage-gated Potassium Channels, in Adult Post-lingual Unilateral Cochlea... | |||||||||||||
Medical condition: Impaired speech understanding in users of cochlear implants | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-004463-44 | Sponsor Protocol Number: CHUB-NAC | Start Date*: 2020-01-22 | |||||||||||
Sponsor Name:CHU Saint Pierre | |||||||||||||
Full Title: Intratympanic injection of N-acetylcysteine for prevention of Cisplatine-induced ototoxicity | |||||||||||||
Medical condition: Ototoxicity | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-005741-17 | Sponsor Protocol Number: 76096 | Start Date*: 2021-08-25 |
Sponsor Name:Amsterdam University Medical Centers, location AMC | ||
Full Title: Hyperbaric OXygen therapy for ACute Acoustic Trauma | ||
Medical condition: Acute acoustic trauma | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: NL (Trial now transitioned) | ||
Trial results: (No results available) |
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: 2012-005002-22 | Sponsor Protocol Number: PROHEARING | Start Date*: 2013-12-06 | |||||||||||
Sponsor Name:Hannover Medical School | |||||||||||||
Full Title: ACEMg mediated hearing preservation in cochlear implant patients receiving different electrode lengths | |||||||||||||
Medical condition: Cochlear implant patients in whom a cochlear implant preserving residual hearing is medically indicated | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-018046-38 | Sponsor Protocol Number: 1-09 | Start Date*: 2010-07-08 |
Sponsor Name:Phafag AG | ||
Full Title: Double blind, placebo-controlled randomized clinical trial to evaluate the efficacy and safety of a transtympanic treatment of tinnitus with caroverine | ||
Medical condition: Caroverine infusions have been used successfully in Austria to treat cochlear-synaptic tinnitus. This treatment is very time consuming and needs a constant monitoring of the physician. This study w... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2012-003685-40 | Sponsor Protocol Number: FPT1530EA | Start Date*: 2012-10-24 | |||||||||||
Sponsor Name:Thoraxkirurgisk afd. Rigshospitalet | |||||||||||||
Full Title: "Doubble blinded RCT comparing 15 versus 30mg Toradol on postoperative VAS-score in ortopedic and ENT patients. | |||||||||||||
Medical condition: Ortopedic and ENT surgery where Toradol is already given | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-002377-19 | Sponsor Protocol Number: 1456/2017 | Start Date*: 2017-09-15 |
Sponsor Name:Abteilung für Hals-, Nasen- und Ohrenkrankheiten MUW, AKH Wien | ||
Full Title: Triamcinolone levels in cochlear perilymph | ||
Medical condition: In this study triamcinolone acetonide levels after intratympanic application in the perilymph, and serum of patients receiving a cochlear implant will be studied. In patients undergoing a translaby... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Completed) | ||
Trial results: View results |
EudraCT Number: 2018-004205-12 | Sponsor Protocol Number: 792 | Start Date*: 2019-02-13 |
Sponsor Name:Region Skåne | ||
Full Title: Methylprednisolone injection in treatment of birch pollen induced allergic rhinitis | ||
Medical condition: Seasonal birch pollen induced allergic rhinitis | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: SE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2013-003049-41 | Sponsor Protocol Number: 50934 | Start Date*: 2014-01-27 |
Sponsor Name:National Institute of Child Health | ||
Full Title: A Phase III, Single-center Clinical Trial to Evaluate the 4-valent HPV Vaccine for the Treatment and Prevention of Recurrent Respiratory Papillomatosis in Children | ||
Medical condition: Recurrant respiratory papillomatosis | ||
Disease: | ||
Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | |
Trial protocol: HU (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2020-005300-19 | Sponsor Protocol Number: 2020 | Start Date*: 2021-03-01 |
Sponsor Name:Medical University Vienna | ||
Full Title: Intracochlear application versus round window instillation of Triamcinolone acetonide in patients with sudden sensorineural hearing loss-a comparative study | ||
Medical condition: Sudden sensorineural hearing loss (SSHL) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2018-000812-47 | Sponsor Protocol Number: SENS401-201 | Start Date*: 2018-09-24 | |||||||||||
Sponsor Name:SENSORION SA | |||||||||||||
Full Title: A two- part, randomized, double-blind, placebo-controlled, parallel-group, efficacy and safety study of SENS-401 in subjects with severe or profound sudden sensorineural hearing loss | |||||||||||||
Medical condition: Sudden sensorineural hearing loss (SSNHL) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SK (Completed) BG (Completed) CZ (Completed) GB (GB - no longer in EU/EEA) DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-004496-71 | Sponsor Protocol Number: 104-201508 | Start Date*: 2016-03-01 | |||||||||||
Sponsor Name:Otonomy Inc. | |||||||||||||
Full Title: A prospective, randomized, double blind, placebo-controlled, multicenter, Phase 3 efficacy and safety study of OTO-104 given as a single intratympanic injection in subjects with unilateral Meniere’... | |||||||||||||
Medical condition: Meniere's disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) BE (Completed) DE (Prematurely Ended) IT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-009605-25 | Sponsor Protocol Number: HANNA4-01 | Start Date*: 2009-09-23 |
Sponsor Name:Hanna Illman | ||
Full Title: " Reversal of neuromuscular blockade by sugammadex during propofol-remifentanil anaesthesia: Does reversal change bispectral index and entropy levels?" | ||
Medical condition: The patients who will be included in this study are scheduled for elective surgery within the field of ear-, nose and throat (ENT) surgery. No particular medical conditions are to be investigated. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FI (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2018-001464-35 | Sponsor Protocol Number: 104-201811 | Start Date*: 2018-11-06 | |||||||||||
Sponsor Name:Otonomy, Inc. | |||||||||||||
Full Title: A prospective, randomized, double blind, placebo-controlled, multicenter, Phase 3 efficacy and safety study of OTO-104 given as a single intratympanic injection in subjects with unilateral Meniere’... | |||||||||||||
Medical condition: Meniere's disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) ES (Ongoing) BE (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2022-000079-38 | Sponsor Protocol Number: DB-OTO-001 | Start Date*: 2023-05-09 | |||||||||||
Sponsor Name:Decibel Therapeutics | |||||||||||||
Full Title: A Phase 1/2, Open-Label, Multicenter Trial With a Single Ascending Dose Cohort With Unilateral Intracochlear Injection Followed by a Bilateral Injection Expansion Cohort to Evaluate the Safety, Tol... | |||||||||||||
Medical condition: Congenital auditory neuropathy secondary to biallelic mutations of the otoferlin gene (hOTOF) | |||||||||||||
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Population Age: Infants and toddlers, Children, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-006497-23 | Sponsor Protocol Number: 870128 | Start Date*: 2022-07-05 |
Sponsor Name:Helsinki University Hospital | ||
Full Title: Corticosteroid in treatment of acute laryngitis among vocal professionals | ||
Medical condition: Laryngitis | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: FI (Trial now transitioned) | ||
Trial results: (No results available) |
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