- Trials with a EudraCT protocol (7)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
7 result(s) found for: Mucopurulent discharge.
Displaying page 1 of 1.
| 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: 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: 2008-003567-39 | Sponsor Protocol Number: LT1225-PIIIB-02/08 | Start Date*: 2008-08-04 |
| Sponsor Name:Laboratoires Thea | ||
| Full Title: clinical efficacy and safety of azyter (azythromycin 1,5%) versus tobramycin 0,3% eye drops in the treatment of purulent bacterial conjonctivitis of children. multicenter, international, investigat... | ||
| Medical condition: This trial will be performed on children aged from one day of life to 18 years old. The medical conditions that will be observed is the purulent bacterial conjonctivitis. | ||
| Disease: | ||
| Population Age: Preterm newborn infants, Newborns, Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | |
| Trial protocol: FR (Completed) BE (Completed) DE (Completed) ES (Completed) PT (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2015-004907-22 | Sponsor Protocol Number: AUG117150 | Start Date*: 2016-08-03 |
| Sponsor Name:Medicines Development (Infectious Diseases) | ||
| Full Title: A multicenter, open-label study to assess the efficacy and safety of potassium clavulanate/amoxicillin (CVA/AMPC 1:14 combination) in the treatment of [Japanese] children with acute bacterial rhin... | ||
| Medical condition: Acute Bacterial Rhinosinusitis | ||
| Disease: | ||
| Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | |
| Trial protocol: Outside EU/EEA | ||
| Trial results: View results | ||
| EudraCT Number: 2015-001952-31 | Sponsor Protocol Number: CRS-03 | Start Date*: 2016-04-14 | |||||||||||
| Sponsor Name:Bionorica SE | |||||||||||||
| Full Title: A multicenter, randomized, double-blind, placebo-controlled, parallel-group clinical trial to assess efficacy and safety of the herbal medicinal product Sinupret extract coated tablets in patients ... | |||||||||||||
| Medical condition: Chronic rhinosinusitis | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2011-003623-35 | Sponsor Protocol Number: CRS-02 | Start Date*: 2012-09-14 |
| Sponsor Name:Bionorica SE | ||
| Full Title: A multicentre, randomized, double-blind, placebo-controlled, parallel group study to assess efficacy and safety of two dosages of a herbal medicinal product (dry extract BNO 1016) in patients with ... | ||
| Medical condition: Chronic Rhinosinusitis | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: PL (Completed) DE (Completed) CZ (Completed) BE (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2018-001780-23 | Sponsor Protocol Number: BTZ116577 | Start Date*: 2019-12-04 |
| Sponsor Name:GlaxoSmithKline Research & Development Limited | ||
| Full Title: A Phase III, Randomized, Multicenter, Open-Label Study in Adolescent and Adult Participants Comparing the Efficacy and Safety of Gepotidacin to Ceftriaxone Plus Azithromycin in the Treatment of Unc... | ||
| Medical condition: Uncomplicated Urogenital Gonorrhea | ||
| Disease: | ||
| Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |
| Trial protocol: GB (GB - no longer in EU/EEA) DE (Completed) | ||
| Trial results: View results | ||
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