- Trials with a EudraCT protocol (8)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
8 result(s) found for: Isopropyl alcohol.
Displaying page 1 of 1.
| EudraCT Number: 2005-005960-95 | Sponsor Protocol Number: 2006UK-001 | Start Date*: 2006-04-26 |
| Sponsor Name:Enturia, Inc. | ||
| Full Title: Prospective, randomised clinical trial to compare the efficacy of 0.5% (w/v) chlorhexidine gluconate in 70% (v/v) isopropyl alcohol with 2% (w/v) chlorhexidine gluconate in 70% (v/v) isopropyl alco... | ||
| Medical condition: This product is a skin disinfectant and therefore is not specific for a medicinal condition. It will be used where patients require skin disinfection prior to surgery and for care of the surgical ... | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: GB (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2004-001086-17 | Sponsor Protocol Number: 2004UK-001 | Start Date*: 2004-10-19 |
| Sponsor Name:Medi-Flex | ||
| Full Title: Prospective randomised clinical trial to assess the efficacy of 70% v/v isopropyl alcohol and 2% w/v chlorhexidine in 70% v/v isopyl alcohol for the disinfection of skin prior to peripheral venous ... | ||
| Medical condition: This product is a skin disinfectant and therefore is not specific for a medical condition. It will be used where patients require skin disinfection prior to peripheral vascular catheterisation | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: GB (Prematurely Ended) | ||
| Trial results: View results | ||
| EudraCT Number: 2010-019984-12 | Sponsor Protocol Number: AMNCH-TCD-CHG-1-2010 | Start Date*: 2010-07-21 |
| Sponsor Name:Adelaide & Meath Hospital, incorporating The National Children's Hospital | ||
| Full Title: A multicentre randomised trial comparing the effects of 2% chlorhexidine gluconate in 70% isopropyl alcohol as a skin, exit site and catheter hub cleansing agent versus other forms of chlorhexidine... | ||
| Medical condition: Prevention of central venous catheter-related infections in haemodialysis patients. This trial will evaluate the effectiveness of 2% chlorhexidine gluconate in 70%isopropyl alcohol as a skin, exit... | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: IE (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2016-002692-98 | Sponsor Protocol Number: GH001 | Start Date*: 2017-10-04 | |||||||||||
| Sponsor Name:GAMA Healthcare | |||||||||||||
| Full Title: An evaluation of the efficacy of HEXI-PREP by Clinell Wipes versus placebo and ChloraPrep, for use in pre-operative skin preparation | |||||||||||||
| Medical condition: For disinfection of the skin, immediately prior to invasive medical procedures | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2012-002460-27 | Sponsor Protocol Number: 1.1 | Start Date*: 2013-02-04 | ||||||||||||||||
| Sponsor Name:ISTITUTO NAZIONALE PER LA CURA TUMORI | ||||||||||||||||||
| Full Title: Preoperative skin preparation to lower surgical site infection in breast cancer surgery: Povidone – iodine 10% aqueous solution versus 2%chlorhexidine in 70% isopropyl alcohol (ChloraPrep, Cardina... | ||||||||||||||||||
| Medical condition: PATIENTS SCHEDULED FOR SURGERY | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Female | |||||||||||||||||
| Trial protocol: IT (Completed) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2015-000874-36 | Sponsor Protocol Number: 2014PAED13L | Start Date*: 2015-10-30 | |||||||||||
| Sponsor Name:Norfolk and Norwich University Hospitals NHS Trust | |||||||||||||
| Full Title: The efficacy and safety of two topical antiseptic solutions for skin disinfection prior to percutaneous central venous catheter insertion in preterm neonates: a feasibility study | |||||||||||||
| Medical condition: Central venous catheter-related sepsis in premature neonates | |||||||||||||
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| Population Age: Preterm newborn infants, Newborns, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2009-016566-82 | Sponsor Protocol Number: 05/SP/120 | Start Date*: 2009-12-29 |
| Sponsor Name:Belfast Health and Social Care Trust [...] | ||
| Full Title: Skin bacteria as a source of surgical infections: molecular epidemiology and prevention of wound contaimination | ||
| Medical condition: No medical condition under investigation, investigation of surgical wound contamination in spinal patients. | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: GB (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2011-002962-19 | Sponsor Protocol Number: SKA 001 | Start Date*: 2011-10-04 |
| Sponsor Name:University College Dublin | ||
| Full Title: CHLORHEXIDINE VERSUS POVIDONE-IODINE FOR SKIN ANITSEPSIS PRIOR TO CENTRAL VENOUS CATHETER INSERTION IN PRETERM INFANTS: PROTOCOL FOR A RANDOMISED TRIAL (THE SKA TRIAL) | ||
| Medical condition: Blood stream infections in neonates | ||
| Disease: | ||
| Population Age: Preterm newborn infants, Under 18 | Gender: Male, Female | |
| Trial protocol: IE (Completed) | ||
| Trial results: View results | ||
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Query did not match any studies.