- Trials with a EudraCT protocol (8)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (3)
8 result(s) found for: Scabies.
Displaying page 1 of 1.
| EudraCT Number: 2022-000660-22 | Sponsor Protocol Number: Benzylbenzoat-Permethrin-5020 | Start Date*: 2022-06-14 |
| Sponsor Name:Landeskrankenhaus Salzburg | ||
| Full Title: Investigation to assess the efficacy of topical benzyl benzoate 10/25% emulsion versus permethrin 5% creme for scabies treatment | ||
| Medical condition: Scabies | ||
| Disease: | ||
| Population Age: Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |
| Trial protocol: AT (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2007-006778-26 | Sponsor Protocol Number: 07ct/am04perm | Start Date*: 2008-07-17 | |||||||||||
| Sponsor Name:gepepharm GmbH | |||||||||||||
| Full Title: Investigation of the local tolerability of pedimitex creme 5% - a permethrine containing creme - in 100 patients with scabies infection of both gender | |||||||||||||
| Medical condition: The product is intended to be used by patients suffering from scabies infestation | |||||||||||||
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| Population Age: Infants and toddlers, Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: BG (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2018-004494-27 | Sponsor Protocol Number: 5020DERM-2018 | Start Date*: Information not available in EudraCT | ||||||||||||||||
| Sponsor Name:Landeskrankenhaus Salzburg | ||||||||||||||||||
| Full Title: pilotstudy- efficacy of infectoscab 5% creme in patients with scabies | ||||||||||||||||||
| Medical condition: Scabies | ||||||||||||||||||
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| Population Age: Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: AT (Completed) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2020-003255-15 | Sponsor Protocol Number: Benzylbenzoat-Ivermectin-5020 | Start Date*: 2020-12-17 |
| Sponsor Name:Landeskrankenhaus Salzburg | ||
| Full Title: Investigation to assess the efficacy of benzyl benzoate 10/25% emulsion versus oral ivermectin for scabies treatment | ||
| Medical condition: Scabies | ||
| Disease: | ||
| Population Age: Infants and toddlers, Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |
| Trial protocol: AT (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2019-001775-37 | Sponsor Protocol Number: MDGH-MOX-2001 | Start Date*: 2019-09-20 | |||||||||||
| Sponsor Name:Medicines Development Limited (trading as Medicines Development for Global Health) | |||||||||||||
| Full Title: A Phase II, randomized, double-blind, parallel group dose finding study of single oral doses of moxidectin in adults with scabies | |||||||||||||
| Medical condition: Scabies (infection with Sarcoptes scabiei) | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Completed) AT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2019-003234-16 | Sponsor Protocol Number: ETSKABI | Start Date*: 2021-01-26 |
| Sponsor Name:InfectoPharm Arzneimittel und Consilium GmbH | ||
| Full Title: Prospektive, offene, multizentrische, initial 1-armige und bei Therapieversagen 3-armig randomisierte klinische Prüfung der Phase III/IV zur eskalierenden Therapie der Skabies mit INFECTOSCAB 5% (P... | ||
| Medical condition: Scabies | ||
| Disease: | ||
| Population Age: Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |
| Trial protocol: DE (Trial now transitioned) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2019-000735-61 | Sponsor Protocol Number: SP-NAC19 | Start Date*: 2021-04-06 | |||||||||||
| Sponsor Name:Dutch Growth Research Foundation | |||||||||||||
| Full Title: N- acetylcysteine treatment for skin picking in children and young adults with PWS: a randomized, controlled, cross-over trial. | |||||||||||||
| Medical condition: Prader-Willi syndrome | |||||||||||||
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| Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: NL (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2018-001219-53 | Sponsor Protocol Number: TR11 | Start Date*: 2019-03-06 | |||||||||||
| Sponsor Name:Trevi Therapeutics, Inc. | |||||||||||||
| Full Title: A Phase 2b/3, Randomized, Double-Blind, Placebo-Controlled, 2-Arm, Efficacy and Safety Study in Prurigo Nodularis with Nalbuphine ER Tablets for Pruritus Relief Through Itch Scratch Modulation (PRI... | |||||||||||||
| Medical condition: Prurigo Nodularis | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) FR (Completed) AT (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
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