- Trials with a EudraCT protocol (20)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
20 result(s) found for: Impetigo.
Displaying page 1 of 1.
EudraCT Number: 2004-004406-24 | Sponsor Protocol Number: TOC103469 | Start Date*: 2005-07-26 | |||||||||||
Sponsor Name:GLAXO SMITHKLINE | |||||||||||||
Full Title: A Randomised, Double-blind, Multicentre, Superiority Placebo-controlled, Phase III Study to Assess the Efficacy and Safety of Topical 1 SB-275833 Ointment versus Placebo Ointment Applied Twice Dai... | |||||||||||||
Medical condition: Treatment of the impetigo | |||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-002219-24 | Sponsor Protocol Number: IMPET-001 | Start Date*: 2020-08-17 | |||||||||||||||||||||||||||||||||||||||||
Sponsor Name:Basic Pharma Technologies | |||||||||||||||||||||||||||||||||||||||||||
Full Title: A Randomized, Double-Blind, Parallel Group, Equivalence, Multicenter Phase III Trial to Compare the Efficacy and Safety of Fusidic Acid Hydrophilic Cream 20 mg/g and Fucidin® Cream in the Treatment... | |||||||||||||||||||||||||||||||||||||||||||
Medical condition: Impetigo contagiosa | |||||||||||||||||||||||||||||||||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||||||||||||
Trial protocol: BE (Completed) CZ (Completed) | |||||||||||||||||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2004-002687-14 | Sponsor Protocol Number: FUC 0301 INT | Start Date*: 2004-11-15 | |||||||||||
Sponsor Name:LEO Pharmaceutical Products Ltd. A/S (LEO Pharma A/S) | |||||||||||||
Full Title: Fucidin® Cream in the Treatment of Impetigo A phase IV study comparing clinical and bacteriological efficacy of Fucidin® cream with Fucidin® cream vehicle in the treatment of impetigo in paediatric... | |||||||||||||
Medical condition: Patients with a clinical diagnosis of impetigo, aged 2-11 years, with a severity score of minimum 1 for at least one of the following signs: Pustules/infected bullae, erythema and infiltration/indu... | |||||||||||||
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Population Age: Children, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-004439-70 | Sponsor Protocol Number: TOC100224 | Start Date*: 2005-05-20 | |||||||||||
Sponsor Name:GlaxSmithKline Research & Development | |||||||||||||
Full Title: A Randomised, Observer-blind, Multicentre, Non-inferiority, Comparative Study of the Safety and Efficacy of Topical 1% SB-275833 Ointment, Applied Twice Daily for 5 Days, versus Topical 2% Sodium F... | |||||||||||||
Medical condition: Impetigo | |||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) IT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-000808-14 | Sponsor Protocol Number: AD-CT-01/05 | Start Date*: 2005-05-24 |
Sponsor Name:Ambria Dermatology | ||
Full Title: A randomized, double-blind, parallell-group, controlled study of topical pentane-1,5-diol hydrogel in patients with impetigo | ||
Medical condition: Impetigo | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | |
Trial protocol: SE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2012-000746-36 | Sponsor Protocol Number: P-100797-01 | Start Date*: 2012-03-28 | |||||||||||
Sponsor Name:Ferrer Internacional, S.A. | |||||||||||||
Full Title: A phase I open-label multiple dose study to examine the systemic bioavailability and safety of twice daily topical applications of ozenoxacin 1% cream formulation in patients with impetigo | |||||||||||||
Medical condition: Impetigo | |||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: Outside EU/EEA | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-004886-98 | Sponsor Protocol Number: TOC110978 | Start Date*: 2017-01-24 | |||||||||||
Sponsor Name:GlaxoSmithKline | |||||||||||||
Full Title: A Randomized, Double-Blind, Double Dummy, Comparative, Multicenter Study to Assess the Safety and Efficacy of Topical Retapamulin Ointment, 1%, versus Oral Linezolid in the Treatment of Secondarily... | |||||||||||||
Medical condition: secondarily-infected traumatic lesions (SITL; excluding abscesses) or impetigo due to methicillin-resistant Staphylococcus aureus (MRSA | |||||||||||||
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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: 2011-003032-31 | Sponsor Protocol Number: P-110880-01 | Start Date*: 2012-02-22 | |||||||||||
Sponsor Name:Ferrer Internacional, S.A. | |||||||||||||
Full Title: A phase III 3 arms, multicenter, randomised, investigator-blind study to assess the efficacy and safety of ozenoxacin 1% cream applied twice daily for 5 days versus placebo in the treatment of pati... | |||||||||||||
Medical condition: Impetigo | |||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-002450-69 | Sponsor Protocol Number: RJ-NBC01 | Start Date*: 2013-11-26 | |||||||||||
Sponsor Name:Laboratorio Reig Jofré S.A | |||||||||||||
Full Title: Estudio de fase III, aleatorizado, abierto con evaluación ciega, multicéntrico, de no-inferioridad, con control activo y con placebo, para evaluar la seguridad y la eficacia de la aplicación tópica... | |||||||||||||
Medical condition: Impetigo | |||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-006151-42 | Sponsor Protocol Number: 0 | Start Date*: 2009-12-17 | |||||||||||||||||||||||||||||||||||||||||
Sponsor Name:Beaumont Hospital | |||||||||||||||||||||||||||||||||||||||||||
Full Title: A comparison of oral flucloxacillin alone with combined oral phenoxymethylpenicillin and flucloxacillin for the treatment of uncomplicated skin and soft tissue infections | |||||||||||||||||||||||||||||||||||||||||||
Medical condition: Infection of the skin and subcutaneous tissues (cellulitis) | |||||||||||||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||||||||||||
Trial protocol: IE (Completed) | |||||||||||||||||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-002528-41 | Sponsor Protocol Number: BPT05-641 | Start Date*: 2006-09-04 |
Sponsor Name:Interdos Pharma bv | ||
Full Title: A comparison of the clinical efficacies of Fusidic acid hydrophilic cream 20 mg/g and Fucidin in the treatment of adult and paediatric patients with impetigo | ||
Medical condition: Impetigo | ||
Disease: | ||
Population Age: Infants and toddlers, Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Completed) BE (Completed) | ||
Trial results: View results |
EudraCT Number: 2008-000036-41 | Sponsor Protocol Number: IPTG-01 | Start Date*: 2014-04-08 | |||||||||||
Sponsor Name:Dermal Laboratories Ltd | |||||||||||||
Full Title: An antimicrobial cream for the treatment of impetigo | |||||||||||||
Medical condition: The condition to be studied is uncomplicated localised primary non-bullous impetigo, suitable for topical antibacterial therapy alone. | |||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-005490-30 | Sponsor Protocol Number: PP21/14 | Start Date*: 2022-04-28 |
Sponsor Name:Hospital Universitario Son Llàtzer | ||
Full Title: EFFECTIVENESS OF TREATMENT WITH ANTISEPTICS VERSUS TOPICAL ANTIBIOTICS IN MILD IMPETIGO IN PEDIATRIC PATIENTS | ||
Medical condition: Impetigo is a bacterial infection of very common skin in the pediatric population. In the usual clinical practice, the treatment of this infection has been based on topical antibiotics. The widespr... | ||
Disease: | ||
Population Age: Children, Under 18 | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2011-002001-30 | Sponsor Protocol Number: IMUP | Start Date*: 2011-12-09 |
Sponsor Name:INFECTOPHARM Arzneimittel und Consilium GmbH | ||
Full Title: Multicenter, prospective, double-blind, two-armed phase III study for efficacy and safety of the topic impetigo therapy of two 2 % mupirocin ointments | ||
Medical condition: Impetigo | ||
Disease: | ||
Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2006-003374-10 | Sponsor Protocol Number: TOC106489 | Start Date*: 2007-08-03 |
Sponsor Name:GlaxoSmithKline Research & Development Ltd | ||
Full Title: An Open-Label, Non-Comparative Study to Assess the Pharmacokinetics, Safety and Efficacy of Topical Retapamulin (SB-275833) Ointment, 1%, Twice Daily for Five Days in the Treatment of Uncomplicated... | ||
Medical condition: Uncomplicated skin and skin structure infections | ||
Disease: | ||
Population Age: Infants and toddlers, Under 18 | Gender: Male, Female | |
Trial protocol: DE (Completed) NL (Completed) | ||
Trial results: View results |
EudraCT Number: 2014-000228-52 | Sponsor Protocol Number: P-110881-01 | Start Date*: 2014-06-03 |
Sponsor Name:Ferrer Internacional, SA | ||
Full Title: A phase III 2 arms, multicenter, randomised, double-blind study to assess the efficacy and safety of ozenoxacin 1% cream applied twice daily for 5 days versus placebo in the treatment of patients w... | ||
Medical condition: Impetigo | ||
Disease: | ||
Population Age: Infants and toddlers, Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Completed) RO (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2015-003972-64 | Sponsor Protocol Number: 2015-09 | Start Date*: 2019-07-02 |
Sponsor Name:ASSISTANCE PUBLIQUE HOPITAUX DE MARSEILLE | ||
Full Title: Plasma and tissue pharmacokinetics of amikacin administrated by dressing impregnated in burns patients | ||
Medical condition: burns patients | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FR (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2007-004980-23 | Sponsor Protocol Number: P05134 | Start Date*: 2008-05-05 | |||||||||||
Sponsor Name:Schering-Plough Farma, Lda. | |||||||||||||
Full Title: Double-Blind evaluation of the safety and efficacy of Quadriderme cream (betamethasone dipropionate, clotrimazole and gentamicin sulphate ) compare with betamethasone dipropionate combined with gen... | |||||||||||||
Medical condition: Impetiginous Eczema | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: PT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-005281-30 | Sponsor Protocol Number: DUR001-306 | Start Date*: 2016-11-03 | ||||||||||||||||||||||||||||||||||||||||||||||
Sponsor Name:Allergan Ltd. | ||||||||||||||||||||||||||||||||||||||||||||||||
Full Title: A Phase 3, Multicenter, Open-Label, Randomized, Comparator Controlled Trial of the Safety and Efficacy of Dalbavancin versus Active Comparator in Pediatric Subjects with Acute Bacterial Skin and Sk... | ||||||||||||||||||||||||||||||||||||||||||||||||
Medical condition: Acute bacterial skin and skin structure infection. For Cohort 5 (from birth to less than 3 months) also patients with sepsis are allowed. | ||||||||||||||||||||||||||||||||||||||||||||||||
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Population Age: Preterm newborn infants, Newborns, Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||||||||||||
Trial protocol: LV (Prematurely Ended) LT (Prematurely Ended) ES (Prematurely Ended) BG (Completed) GR (Completed) PL (Completed) | ||||||||||||||||||||||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2009-011931-11 | Sponsor Protocol Number: H 552 000 - 0911 | Start Date*: Information not available in EudraCT | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Sponsor Name:Almirall Hermal GmbH | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Full Title: Explorative, double-blind, randomized, controlled multi-center phase II study to evaluate the efficacy and safety of topically applied combinational product LAS41003 once daily versus corresponding... | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Medical condition: Patients aged 18 and older suffering from at least one clinically diagnosed superinfected or impetiginised eczema such as e.g. • superinfected or impetiginised atopic eczema • superinfected or impe... | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial protocol: DE (Completed) | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial results: View results |
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