- Trials with a EudraCT protocol (4)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
4 result(s) found for: Silver sulfadiazine.
Displaying page 1 of 1.
EudraCT Number: 2013-005124-42 | Sponsor Protocol Number: KEKLUKACS-CLIN-02 | Start Date*: 2014-03-17 |
Sponsor Name:Lukács és Társa Gyógyszerkereskedelmi Betéti Társaság | ||
Full Title: A Phase II/III Adaptive, Seamless, Prospective, Randomized, Controlled, Parallel, Open Multicenter Study to Assess the Safety and Efficacy of Kék Lukács Ointment Compared to Standard Silver Sulfadi... | ||
Medical condition: Partial thickness (second-degree) burns. Total study target burn area: > 25 cm2 < 400 cm2 (or 2% of TBSA), and the burn therapy begun within 6-72 hours. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: HU (Completed) | ||
Trial results: View results |
EudraCT Number: 2014-000714-65 | Sponsor Protocol Number: PHAGOBURN | Start Date*: 2015-06-24 |
Sponsor Name:Pherecydes Pharma SA | ||
Full Title: Evaluation of phage therapy for the treatment of Pseudomonas aeruginosa wound infections in burned patients (Phase I-II clinical trial) | ||
Medical condition: P. aeruginosa infected wound in burned patients. | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: View results |
EudraCT Number: 2011-005037-39 | Sponsor Protocol Number: KEKLUKACS-CLIN-01 | Start Date*: 2012-04-17 |
Sponsor Name:Lukács és Társa Gyógyszerkereskedelmi Betéti Társaság | ||
Full Title: A Phase II Randomized, Controlled Parallel-Group Pilot Study to Assess the Safety and Efficacy of Kék Lukács Ointment Compared to Standard Silver Sulphadiazine (Dermazin®, SSD) Therapy in the Wound... | ||
Medical condition: Patients with burn injuries confined to the trunk and/or upper and lower extremities. Total burn area for all burns on a single patient should be no greater than 15% of TBSA. Patients’ total study ... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: HU (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2013-000901-21 | Sponsor Protocol Number: 2013.03 | Start Date*: 2013-10-24 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Sponsor Name:Rode Kruis Ziekenhuis | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Full Title: A randomized clinical trial on the effectiveness, cost-effectiveness and quality of life of Flaminal® versus Flammazine® in the treatment of superficial and deep partial thickness burns | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Medical condition: Patients with partial thickness burns and/ or mixed depth of partial and full thickness burns | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial protocol: NL (Ongoing) | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial results: (No results available) |
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