- Trials with a EudraCT protocol (7)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
7 result(s) found for: Verruca vulgaris.
Displaying page 1 of 1.
| EudraCT Number: 2007-006738-33 | Sponsor Protocol Number: CL-1205 | Start Date*: 2008-03-14 | |||||||||||
| Sponsor Name:NatImmune A/S | |||||||||||||
| Full Title: bLAC - A phase II double-blind, placebo controlled, clinical proof of concept trial of the efficacy of 8 weeks treatment of cutaneous warts with bLAC in immune suppressed, kidney transplanted patients | |||||||||||||
| Medical condition: Cutaneous wart lesions on hands and/or feet at immune suppressed, kidney transplanted patients. | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DK (Completed) SE (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2009-012210-48 | Sponsor Protocol Number: 20407 | Start Date*: 2009-08-06 | ||||||||||||||||
| Sponsor Name:Leiden University Medical Centre | ||||||||||||||||||
| Full Title: Monochloroacetic acid versus cryotherapy in the treatment of warts: A Randomised Clinical Trial (WARTS-2) | ||||||||||||||||||
| Medical condition: All patients from the age of 4 onward, who present themselves to their practice with one or more new warts of the type vulgaris on hands or feet. | ||||||||||||||||||
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| Population Age: Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: NL (Ongoing) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2009-016302-16 | Sponsor Protocol Number: DPSI-IDP-109-P2-01 | Start Date*: 2010-03-19 | |||||||||||
| Sponsor Name:Dow Pharmaceutical Sciences Inc. | |||||||||||||
| Full Title: A Randomized, Double-Blind, Vehicle-Controlled Study Evaluating the Safety and Efficacy of IDP-109 Solution in the Treatment of Patients with Verrucae Vulgares | |||||||||||||
| Medical condition: Verrucae vulgares | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2014-003688-39 | Sponsor Protocol Number: CLS003-CO-PR-002 | Start Date*: 2014-11-26 | ||||||||||||||||
| Sponsor Name:Cutanea Life Sciences | ||||||||||||||||||
| Full Title: A Phase 2, Randomized, Vehicle-Controlled, Double-Blind, Proof-of-Concept Study to Evaluate Efficacy and Safety of Topical Ionic Contra-viral Therapy (ICVT) Comprised of Digoxin and Furosemide in C... | ||||||||||||||||||
| Medical condition: Patients with at least two warts who are otherwise healthy subjects | ||||||||||||||||||
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| Population Age: Adults | Gender: Male, Female | |||||||||||||||||
| Trial protocol: NL (Completed) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2008-004044-36 | Sponsor Protocol Number: 2008-213 | Start Date*: 2008-09-02 | ||||||||||||||||
| Sponsor Name:Bispebjerg Hospital | ||||||||||||||||||
| Full Title: Behandling af præmaligne hudlæsioner med topikal imiquimod og fotodynamisk terapi hos organtransplanterede patienter - et randomiseret intraindividuelt forsøg med blindet effektvurdering | ||||||||||||||||||
| Medical condition: Aktiniske keratoser og virale vorter | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: DK (Completed) SE (Completed) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2008-006863-35 | Sponsor Protocol Number: 314759 | Start Date*: 2013-10-01 | |||||||||||||||||||||
| Sponsor Name:Bispebjerg Hospital | |||||||||||||||||||||||
| Full Title: Prophylactic photodynamic therapy for organ transplant patients – a randomised, intra-individual trial with blinded outcome evaluation. | |||||||||||||||||||||||
| Medical condition: Development of actinic keratoses and skin cancer in kidney transplant patients - a randomised, intra-individual trial with blinded outcome evaluation. | |||||||||||||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||||||||||||
| Trial protocol: SE (Completed) | |||||||||||||||||||||||
| Trial results: (No results available) | |||||||||||||||||||||||
| EudraCT Number: 2019-001443-52 | Sponsor Protocol Number: LLB-2019-02 | Start Date*: 2019-11-13 | ||||||||||||||||||||||||||
| Sponsor Name:LABO'LIFE Belgium sprl | ||||||||||||||||||||||||||||
| Full Title: Randomized study to evaluate 2LVERU® JUNIOR and 2LVERU® efficacy on the treatment of warts. Protocol EVAsION | ||||||||||||||||||||||||||||
| Medical condition: Non genital warts infection | ||||||||||||||||||||||||||||
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| Population Age: Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
| Trial protocol: BE (Trial now transitioned) | ||||||||||||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||||||||||||
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