- Trials with a EudraCT protocol (122)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (44)
122 result(s) found for: Actinic Keratosis.
Displaying page 1 of 7.
EudraCT Number: 2006-005034-20 | Sponsor Protocol Number: 228-13/06 | Start Date*: 2007-03-08 | |||||||||||
Sponsor Name:Klinik für Dermatologie und Venerologie, Universitätsklinikum Hamburg-Eppendorf | |||||||||||||
Full Title: Doppelblinde, prospektiv-randomisierte, intraindividuell-halbseitenvergleichende Studie zur klinischen Wirksamkeit von Verrumal® Lsg. bei aktinischen Keratosen gegen Vehikel: Investigator-initiiert... | |||||||||||||
Medical condition: Actinic keratosis is a precancerous skin growth usually caused by sun exposure. Symptoms: Rough and dry textured skin lesion, macule, patch, or growth on the skin Located on sun-exposed areas. Acti... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-005525-33 | Sponsor Protocol Number: HDP 606 | Start Date*: 2007-03-21 | |||||||||||
Sponsor Name:Heidelberg Pharma GmbH | |||||||||||||
Full Title: A Multi-Centre Double-Blind Randomised Placebo-Controlled Phase II Study of HDP 99.0006 in Patients with Actinic Keratosis | |||||||||||||
Medical condition: Actinic Keratosis are scaling epidermal lesions, which consist of dysplastic keratinocytes. They mostly appear in pale-skinned patients which are chronically overexposed to UV radiation. Actinic ke... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-005996-37 | Sponsor Protocol Number: JAZ-02 | Start Date*: 2022-01-18 | |||||||||||
Sponsor Name:Zealand University Hospital | |||||||||||||
Full Title: Gene and protein expression profiles after treatment of actinic keratosis | |||||||||||||
Medical condition: Actinic keratoses | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-001389-40 | Sponsor Protocol Number: phch2013 | Start Date*: 2014-04-29 | |||||||||||
Sponsor Name:Mari Grönroos | |||||||||||||
Full Title: Daylight-PDT in the treatment of actinic keratosis: a pilot study comparing two different light sensitizers | |||||||||||||
Medical condition: actinic keratoses of the scalp | |||||||||||||
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Population Age: Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-003316-27 | Sponsor Protocol Number: 12020 | Start Date*: 2021-04-01 | |||||||||||
Sponsor Name:Medical University of Graz | |||||||||||||
Full Title: Earliest Stage Treatment of Actinic Keratosis with Imiquimod 3.75% Cream | |||||||||||||
Medical condition: Actintic keratosis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-002108-15 | Sponsor Protocol Number: no_nbr | Start Date*: 2013-06-05 | |||||||||||
Sponsor Name:Mari Grönroos | |||||||||||||
Full Title: Treating actinic keratoses with natural daylight PDT: comparing two light sensitizers (ALA vs. MAL) | |||||||||||||
Medical condition: actinic keratoses of the face or scalp | |||||||||||||
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Population Age: Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-002756-11 | Sponsor Protocol Number: 43739 | Start Date*: 2014-08-27 | |||||||||||
Sponsor Name:Department of Dermatology D92, Bispebjerg Hospital | |||||||||||||
Full Title: Photodynamic therapy with varying application times for treatment of actinic keratosis | |||||||||||||
Medical condition: Actinic keratosis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-003003-29 | Sponsor Protocol Number: 49301 | Start Date*: 2015-08-31 | |||||||||||
Sponsor Name:Department of Dermatology D92, Bispebjerg Hospital | |||||||||||||
Full Title: 5-flourouracil treatment prior to photodynamic therapy of actinic keratosis on the hands | |||||||||||||
Medical condition: Actinic keratosis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-000228-85 | Sponsor Protocol Number: LP0084-1369 | Start Date*: 2017-05-30 | |||||||||||
Sponsor Name:LEO Pharma A/S | |||||||||||||
Full Title: Incidence of squamous cell carcinoma and other skin neoplasia in subjects with actinic keratosis treated with ingenol disoxate gel 0.018% or 0.037%, or vehicle A phase 3 trial to compare the inc... | |||||||||||||
Medical condition: Actinic Keratosis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) DE (Prematurely Ended) ES (Prematurely Ended) IT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-000093-23 | Sponsor Protocol Number: H 565000 - 0620 | Start Date*: 2007-05-18 | |||||||||||
Sponsor Name:Almirall Hermal GmbH | |||||||||||||
Full Title: Clinical trial to investigate clinical efficacy and tolerability of Tretinoin in actinic keratosis | |||||||||||||
Medical condition: actinic keratosis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-005432-24 | Sponsor Protocol Number: H 10056002-0615 | Start Date*: 2007-03-09 | |||||||||||
Sponsor Name:Hermal Kurt Herrmann GmbH & Co OHG | |||||||||||||
Full Title: Clinical trial to investigate clinical efficacy and tolerability of Verrumal in actinic keratosis (PoC) | |||||||||||||
Medical condition: actinic keratosis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-003020-31 | Sponsor Protocol Number: 24-08-2015version3.0 | Start Date*: 2015-09-03 | |||||||||||
Sponsor Name:Department of Dermatology, Bispebjerg University Hospital | |||||||||||||
Full Title: Pulse-Daylight-Photodynamic Therapy of Actinic Keratoses | |||||||||||||
Medical condition: Actinic keratoses | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-002450-12 | Sponsor Protocol Number: LP0084-1194 | Start Date*: 2016-01-04 | |||||||||||
Sponsor Name:LEO Pharma A/S | |||||||||||||
Full Title: Efficacy and Safety of LEO 43204 in Field Treatment of Actinic Keratosis on Face or Chest including 12-month follow-up Part 1: 3-day treatment period including an 8-week follow-up period Part 2:... | |||||||||||||
Medical condition: Actinic Keratosis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-002501-39 | Sponsor Protocol Number: 201073 | Start Date*: 2009-02-06 | ||||||||||||||||
Sponsor Name:MedaPharma | ||||||||||||||||||
Full Title: Quality of life of patients with actinic keratoses and/or a superficial basal cell carcinoma treated with Imiquimod 5% cream. | ||||||||||||||||||
Medical condition: patients with actinic keratoses and/or a superficial basal cell carcinoma | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: NL (Ongoing) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-001701-33 | Sponsor Protocol Number: 58161 | Start Date*: 2017-05-19 | |||||||||||
Sponsor Name:Department of Dermatology D92, Bispebjerg Hospital | |||||||||||||
Full Title: Photodynamic therapy without curettage | |||||||||||||
Medical condition: Actinic keratosis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-005084-14 | Sponsor Protocol Number: 56297 | Start Date*: 2017-01-23 | |||||||||||
Sponsor Name:Deoartment of Dermatology D92, Bispbjerg Hospital | |||||||||||||
Full Title: PpIX in curetted and non-curetted skin after Metvix application | |||||||||||||
Medical condition: Actinic keratosis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-022502-40 | Sponsor Protocol Number: PLES-AK-P-4/12/10 | Start Date*: 2010-10-28 | |||||||||||
Sponsor Name:Pantec Biosolution AG | |||||||||||||
Full Title: Prospektive, randomisierte, klinische 4-Arm Pilotstudie zur Dosisfin-dung der kombinierten Anwendung von P.L.E.A.S.E. mit 5% topischen Imiquimod versus Standardapplikation von 5% topischem Imiquim... | |||||||||||||
Medical condition: Actinic Keratosis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-002849-59 | Sponsor Protocol Number: 2015PQ01 | Start Date*: 2018-02-07 | ||||||||||||||||
Sponsor Name:University of Dundee [...] | ||||||||||||||||||
Full Title: A randomised double blind, placebo controlled study of the efficacy of topical menthol for pain relief during topical photodynamic therapy. | ||||||||||||||||||
Medical condition: Actinic keratosis (pre-cancerous sun damage)on the face and scalp | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (Prematurely Ended) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2005-005171-14 | Sponsor Protocol Number: | Start Date*: 2008-01-07 | |||||||||||
Sponsor Name:NHS Tayside | |||||||||||||
Full Title: A Randomised Double Blind Comparative Study of Pain During and After MAL or 5-ALA Photodynamic Therapy | |||||||||||||
Medical condition: Bowen's disease (sqaumous cell carcinoma in-situ) and actinic keratoses | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-003613-28 | Sponsor Protocol Number: CLFX453X2201 | Start Date*: 2014-12-17 | |||||||||||
Sponsor Name:Novartis Pharma Services AG | |||||||||||||
Full Title: A randomized, vehicle controlled, active comparator, parallel group study to evaluate safety, tolerability and preliminary efficacy of topical LFX453 formulations in patients with actinic keratosis | |||||||||||||
Medical condition: Actinic keratosis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Completed) IS (Completed) DE (Completed) DK (Completed) GB (Completed) | |||||||||||||
Trial results: View results |
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