- Trials with a EudraCT protocol (4)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
4 result(s) found for: Applied physiology.
Displaying page 1 of 1.
EudraCT Number: 2020-001318-39 | Sponsor Protocol Number: UNIHHSkinQuality202000401 | Start Date*: 2021-04-30 |
Sponsor Name:Prof. Dr. Martina Kerscher, University of Hamburg | ||
Full Title: Skin perception after intradermal application of IncobotulinumtoxinA within upper and midface (Interventional Phase II) | ||
Medical condition: Skin perception after intradermal application of INCOBOTULINUMTOXIN A within upper and midface | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: DE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2014-004552-64 | Sponsor Protocol Number: 131016 | Start Date*: 2017-07-03 |
Sponsor Name:Center for Digestive Diseases, Karolinska University Hospital | ||
Full Title: MISTRAL - Mistletoe therapy in primary and recurrent inoperable pancreatic cancer - A phase III prospective, randomized, double blinded, multicenter, parallel group, placebo controlled clinical tr... | ||
Medical condition: Primary or recurrent inoperable pancreatic cancer | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: SE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2016-003802-14 | Sponsor Protocol Number: CRC-PSO-SKINPEN-A-27 | Start Date*: 2016-11-25 | |||||||||||
Sponsor Name:Charité - Universitätsmedizin Berlin | |||||||||||||
Full Title: Skin penetration of anti-inflammatory compounds in lesional compared to non-lesional skin of psoriasis patients | |||||||||||||
Medical condition: Psoriasis vulgaris | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: DE (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-001821-85 | Sponsor Protocol Number: CRAD001H2304 | Start Date*: 2008-01-04 | |||||||||||||||||||||
Sponsor Name:Novartis Pharma Services AG | |||||||||||||||||||||||
Full Title: A 24 month, multi-center, open-label, randomized, controlled study to evaluate the efficacy and safety of concentration controlled everolimus to eliminate or to reduce tacrolimus compared to tacrol... | |||||||||||||||||||||||
Medical condition: Immunosuppression in liver transplantation | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: SE (Completed) NL (Completed) FR (Completed) BE (Prematurely Ended) HU (Completed) ES (Completed) IE (Completed) IT (Completed) GB (Completed) DE (Completed) CZ (Completed) | |||||||||||||||||||||||
Trial results: View results |
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