- 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 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
					
						
							
  | 
			||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Trial protocol: NL (Ongoing) | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
			Subscribe to this Search
To subscribe to the RSS feed for this search click here
			.
			This will provide an RSS feed for clinical trials matching your search that have been added or updated in the last 7 days.
		
			
To subscribe to the RSS feed for this search click here
			.
			This will provide an RSS feed for clinical trials matching your search that have been added or updated in the last 7 days.
		| Download Options: | |
|---|---|
| Number of Trials to download: | |
| Download Content: | |
| Download Format: | |
| Note, where multi-state trials are shown in search results, selecting "Full Trial details" will download full information for each of the member states/countries involved in the trial. | |
    	Query did not match any studies.