- Trials with a EudraCT protocol (8)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
		
	   		
	   		    
                    
                   	
                   	    8 result(s) found for: Asepsis.
                    
                
			
   			
		
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| EudraCT Number: 2020-002325-28 | Sponsor Protocol Number: D-PLEX311 | Start Date*: 2020-09-23 | |||||||||||
| Sponsor Name:PolyPid Ltd. | |||||||||||||
| Full Title: Phase III, Prospective, Multinational, Multicenter, Randomized, Controlled, Two‐arm, Double Blind Study to assess Efficacy and Safety of D‐PLEX Administered Concomitantly with the Standard of Care ... | |||||||||||||
| Medical condition: Prevention of post abdominal surgery incisional infection | |||||||||||||
| 
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: BG (Completed) CZ (Completed) HR (Completed) HU (Completed) SK (Completed) PL (Completed) RO (Ongoing) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2020-003617-36 | Sponsor Protocol Number: D-PLEX312 | Start Date*: 2020-12-13 | |||||||||||
| Sponsor Name:PolyPid Ltd. | |||||||||||||
| Full Title: Phase III, Prospective, Multinational, Multicenter, Randomized, Controlled, Two-arm, Double Blind Study to Assess Efficacy and Safety of D-PLEX Administered Concomitantly with the Standard of Care ... | |||||||||||||
| Medical condition: Prevention of post abdominal surgery incisional infection. | |||||||||||||
| 
 | |||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: HU (Trial now transitioned) PL (Trial now transitioned) DE (Trial now transitioned) IE (Trial now transitioned) PT (Trial now transitioned) IT (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2009-010173-20 | Sponsor Protocol Number: A3051113 | Start Date*: 2009-08-06 | |||||||||||
| Sponsor Name:Pfizer Limited, Ramsgate Road, Sandwich, Kent, CT13 9NJ, UK | |||||||||||||
| Full Title: A MULTICENTER, OPEN LABEL STUDY TO INVESTIGATE THE FEASIBILITY AND EFFICACY OF A SMOKING CESSATION PROGRAM WITH VARENICLINE IN PATIENTS UNDERGOING ELECTIVE SURGERY | |||||||||||||
| Medical condition: Smoking cessation in patients scheduled for elective surgery. | |||||||||||||
| 
 | |||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Prematurely Ended) FR (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2019-002207-17 | Sponsor Protocol Number: D-PLEX-302 | Start Date*: 2020-07-14 | |||||||||||
| Sponsor Name:PolyPid Ltd. | |||||||||||||
| Full Title: A Phase III, Prospective, Multinational, Multicenter, Randomized, Parallel Controlled, Two arms, Single Blind, Study to Assess the Efficacy and Safety of D-PLEX Administered Concomitantly with the ... | |||||||||||||
| Medical condition: Prevention of Post-Cardiac Surgery Sternal Infections | |||||||||||||
| 
 | |||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: HU (Prematurely Ended) IT (Prematurely Ended) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2004-004214-16 | Sponsor Protocol Number: FS014 | Start Date*: 2005-01-19 | |||||||||||
| Sponsor Name:Committee of Management, Common Services Agency T/A Scottish National Blood Transfusion Service | |||||||||||||
| Full Title: A randomised control clinical study to determine whether SNBTS Fibrin Sealant promotes wound healing in patients undergoing cardiac surgery. | |||||||||||||
| Medical condition: In patients undergoing cardiac surgery the saphenous leg vein is used to replace veins used in coronary artery bypass grafts (CABG) surgery. | |||||||||||||
| 
 | |||||||||||||
| Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2011-000090-32 | Sponsor Protocol Number: BBR-012CS01 | Start Date*: 2011-05-12 | |||||||||||
| Sponsor Name:Bridge BioResearch Rights (Jersey) Ltd | |||||||||||||
| Full Title: A Randomised, Double-Blind, Repeat-Dose, Placebo-Controlled Phase IIa Proof of Concept Study to Investigate the Safety and Efficacy of Oral BBR-012 in Combination With Standard Medical Care in Diab... | |||||||||||||
| Medical condition: Complicated skin ulceration on the foot in patients with diabetes. | |||||||||||||
| 
 | |||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2007-004397-62 | Sponsor Protocol Number: PI070274 | Start Date*: 2008-11-28 | |||||||||||
| Sponsor Name:Servicio Andaluz de Salud | |||||||||||||
| Full Title: Análisis aleatorizado y doble ciego sobre la utilidad del extracto de arándano rojo vs profilaxis antibiótica con Trimetoprima en la infección urinaria recurrente infantil | |||||||||||||
| Medical condition: First clinical assay so far where the convenience is evaluated of carrying out prophylaxis of the pediatric urinary recurrent infection in the childhood with extract of cranberries (with a fixed co... | |||||||||||||
| 
 | |||||||||||||
| Population Age: Infants and toddlers, Children, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2008-004537-19 | Sponsor Protocol Number: 2008-004537-19 | Start Date*: 2009-08-03 | ||||||||||||||||||||||||||
| Sponsor Name:Karolinska Universitetssjukhuset | ||||||||||||||||||||||||||||
| Full Title: Effekt av insulininfusion på sjukdomsförloppet vid infekterade fotsår samt vid thorax- och kärlkirurgi hos patienter med diabetes | ||||||||||||||||||||||||||||
| Medical condition: diabetes mellitus infekterat fotsår kärl eller thoraxkirurgisk operation | ||||||||||||||||||||||||||||
| 
 | ||||||||||||||||||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
| Trial protocol: SE (Ongoing) | ||||||||||||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||||||||||||
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