- Trials with a EudraCT protocol (7)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
7 result(s) found for: Occlusive Dressing.
Displaying page 1 of 1.
EudraCT Number: 2005-003806-27 | Sponsor Protocol Number: None avaliable | Start Date*: 2005-10-13 |
Sponsor Name:Princess Alexandra Hospital | ||
Full Title: Is potent topical corticosteroid ointment covered by a plastic film dressing more effective than using potent corticosteroid ointment alone in children with atopic dermatitis? | ||
Medical condition: Children aged 1-15 years with Atopic Dermatitis | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |
Trial protocol: GB (GB - no longer in EU/EEA) | ||
Trial results: (No results available) |
EudraCT Number: 2013-003104-39 | Sponsor Protocol Number: SIS-05-2013 | Start Date*: 2013-12-18 |
Sponsor Name:FakultnĂ nemocnice Ostrava,Czech republic | ||
Full Title: Randomised Clinical Study of Safety of Efficacy of Extracelular Matrix and Autologous Platelet Rich Plasma Concentrate for Wound Healing (Leg Ulcers Biodesign Wound Healing – LEGEND(A) Study) In... | ||
Medical condition: Chronical ischemic and venous ulcers | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: CZ (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2011-001312-59 | Sponsor Protocol Number: CRO1824 | Start Date*: 2011-06-24 | |||||||||||
Sponsor Name:Imperial College London | |||||||||||||
Full Title: A double-blinded, randomized, crossover clinical study to assess the efficacy of Qutenza (capsaicin 8% patches) for the reduction of site pain caused by continuous subcutaneous infusion of Remoduli... | |||||||||||||
Medical condition: Pulmonary arterial hypertension (PAH) is a rare life-threatening disease characterised by high blood pressure in the arteries to the lungs, rapidly evolving in a clinical syndrome of dyspnoea and f... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-001724-19 | Sponsor Protocol Number: CLI-06467AA1-01 | Start Date*: 2018-10-04 | |||||||||||
Sponsor Name:Chiesi Farmaceutici S.p.A. | |||||||||||||
Full Title: A randomised, double-blind, placebo-controlled study to investigate the safety, tolerability, pharmacokinetic and pharmacodynamic profiles of CHF6467 after single and repeated ascending doses in su... | |||||||||||||
Medical condition: Diabetic Neuropathic Foot Ulcers (DFU) Texas Scale Grade 1A and 2A | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BG (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-005386-67 | Sponsor Protocol Number: 20140318 | Start Date*: 2017-03-27 | ||||||||||||||||
Sponsor Name:Amgen Inc. | ||||||||||||||||||
Full Title: A Phase 1b/2, Multicenter, Open-label, Basket Trial to Evaluate the Safety of Talimogene Laherparepvec Injected into Liver Tumors Alone and in Combination With Systemic Pembrolizumab in Phase 1b an... | ||||||||||||||||||
Medical condition: Hepatocellular carcinoma (HCC) and metastatic liver tumors (non-HCC) | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: BE (Completed) DE (Completed) AT (Completed) PL (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-002794-35 | Sponsor Protocol Number: CPDR001F2301 | Start Date*: 2017-02-20 | |||||||||||
Sponsor Name:Novartis Pharma AG | |||||||||||||
Full Title: A randomized, double-blind, placebo-controlled, phase III study comparing the combination of PDR001, dabrafenib and trametinib versus placebo, dabrafenib and trametinib in previously untreated pati... | |||||||||||||
Medical condition: Unresectable or metastatic BRAF V600 mutant melanoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) SE (Completed) GB (GB - no longer in EU/EEA) ES (Ongoing) AT (Completed) CZ (Ongoing) PL (Ongoing) BG (Completed) GR (Completed) BE (Completed) PT (Completed) NL (Ongoing) DK (Completed) HU (Ongoing) IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-004104-34 | Sponsor Protocol Number: SNDX-5613-0700 | Start Date*: 2022-04-20 | |||||||||||
Sponsor Name:Syndax Pharmaceuticals, Inc | |||||||||||||
Full Title: A Phase 1/2, Open-label, Dose-Escalation and Dose-Expansion Cohort Study of SNDX-5613 in Patients with Relapsed/Refractory Leukemias, Including Those Harboring an MLL/KMT2A Gene Rearrangement or Nu... | |||||||||||||
Medical condition: Relapsed or Refractory Acute Leukemias | |||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Ongoing) ES (Ongoing) LT (Ongoing) DE (Temporarily Halted) IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
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