- Trials with a EudraCT protocol (51)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (105)
51 result(s) found for: Chlorhexidine.
Displaying page 1 of 3.
| EudraCT Number: 2020-002751-38 | Sponsor Protocol Number: PREPREP | Start Date*: 2021-02-01 |
| Sponsor Name:Region Östergötland | ||
| Full Title: Long-term effect of chlorhexidine gluconate 4% and Chlorhexidine alcohol 5 mg /ml on growth and recolonisation of bacteria on the skin | ||
| Medical condition: Cutaneous antibacterial efficacy in healthy volunteers. | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: SE (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2019-003604-12 | Sponsor Protocol Number: ITM201902 | Start Date*: 2020-01-15 | |||||||||||
| Sponsor Name:Institute of Tropical Medicine | |||||||||||||
| Full Title: Evaluation of a chlorhexidine mouthwash for the eradication of asymptomatic pharyngeal Neisseria gonorrhoeae infection | |||||||||||||
| Medical condition: asymptomatic pharyngeal Neisseria gonorrhoeae (NG) | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male | ||||||||||||
| Trial protocol: BE (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: 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: 2016-005027-81 | Sponsor Protocol Number: 0 | Start Date*: 2018-08-14 |
| Sponsor Name:Maria Siponen [...] | ||
| Full Title: Chlorhexidine and nystatin in the treatment of oral candidosis - a pilot study | ||
| Medical condition: oral candidosis | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: FI (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2006-000675-15 | Sponsor Protocol Number: 06RP02 | Start Date*: 2006-09-11 |
| Sponsor Name:Great Ormond Street Hospital for Children NHS Trust | ||
| Full Title: Open label Randomised Controlled Trial comparing povidone-iodine 10% with alcohol and 0.5% chlorhexidine with alcohol for prevention of early infection associated with insertion of central venous a... | ||
| Medical condition: Potential Systematic Sepsis | ||
| Disease: | ||
| Population Age: Preterm newborn infants, Newborns, Infants and toddlers, Children, Adolescents, Under 18, Adults | Gender: Male, Female | |
| Trial protocol: GB (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2012-002236-87 | Sponsor Protocol Number: RH01561 | Start Date*: 2012-08-16 | ||||||||||||||||
| Sponsor Name:GlaxoSmithKline Consumer Healthcare | ||||||||||||||||||
| Full Title: Clinical Study to Evaluate the Efficacy of Chlorhexidine Mouthwashes | ||||||||||||||||||
| Medical condition: Gingival bleeding and gingivitis | ||||||||||||||||||
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| Population Age: Adults | 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: 2007-002624-15 | Sponsor Protocol Number: FERTOMCIDINA | Start Date*: 2007-06-28 | |||||||||||
| Sponsor Name:AZIENDA SANITARIA OSPEDALIERA "S. GIOVANNI BATTISTA DI TORINO" | |||||||||||||
| Full Title: Fertomcidina ﾓUﾔ vs chlorhexidine 0.2% in recurrent aphthous stomatitis: randomized comparative double-blind study. | |||||||||||||
| Medical condition: patients with recurrent aphthous stomatitis | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2012-000260-17 | Sponsor Protocol Number: Intermed_Chlorhexidine_sol_0.2%_ | Start Date*: 2012-09-07 | |||||||||||||||||||||
| Sponsor Name:IOULIA & IRENE TSETI PHARMACEUTICAL LABORATORIES S.A.-INTERMED S.A. | |||||||||||||||||||||||
| Full Title: A therapeutic equivalence study, comparing two chlorhexidine digluconate formulations, the test formulation Chlorel® Or. T. Sol. 0,2% w / v and the reference formulation Corsodyl® 0.2% w / v Mint M... | |||||||||||||||||||||||
| Medical condition: Therapeutic equivalence study, comparing two chlorhexidine digluconate formulations indicated for inhibition of the formation of dental plaque, as an aid in the treatment and prevention of gingivi... | |||||||||||||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||||||||||||
| Trial protocol: GR (Completed) | |||||||||||||||||||||||
| Trial results: View results | |||||||||||||||||||||||
| EudraCT Number: 2013-000383-28 | Sponsor Protocol Number: CLI/016P | Start Date*: 2015-01-12 |
| Sponsor Name:Dexcel Pharma Technologies Ltd. | ||
| Full Title: The Efficacy and Safety of Chlorhexidine Gluconate Chip (PerioChip®) in Therapy of Peri-implantitis | ||
| Medical condition: Peri-implantitis | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: GB (Completed) DE (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2006-005649-12 | Sponsor Protocol Number: SUCPAT1_CTR0026 | Start Date*: 2006-12-20 |
| Sponsor Name:Regent Medical | ||
| Full Title: A 96 hour (4-application) patch test and TEWL assessment in healthy volunteers to investigate the comparative skin irritation potential of six antiseptics and two controls following cutaneous patch... | ||
| Medical condition: This trial will be carried out on healthy volunteers. Patches containing 0.2mls of each test product will be used. Each volunteer will have a single patch per product and the patches will be remov... | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: GB (GB - no longer in EU/EEA) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2010-020206-14 | Sponsor Protocol Number: 09.0058 | Start Date*: 2011-01-31 |
| Sponsor Name:St George's University of London | ||
| Full Title: Evaluation study of Meticillin Resistant Staphylococcus aureus (MRSA) during routine nasal decolonisation programmes with Bactroban Nasal® ointment, Chlorhexidine Gluconate 4% body and hair wash, a... | ||
| Medical condition: MRSA | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: GB (Prematurely Ended) | ||
| 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: 2014-004682-24 | Sponsor Protocol Number: DC0071BB405 | Start Date*: 2015-04-27 | |||||||||||
| Sponsor Name:Institut de Recherche Pierre Fabre - Centre de R&D Pierre Fabre | |||||||||||||
| Full Title: Efficacy of DC071 mouthwash (0,2 % chlorhexidine digluconate) in peri-surgical care for preventing alveolar osteitis after third molar extraction. Prospective, multicenter, randomised, double-blin... | |||||||||||||
| Medical condition: Prevention of alveolar osteitis after third molar extraction | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: EE (Completed) LV (Completed) LT (Completed) FR (Completed) ES (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2009-016571-30 | Sponsor Protocol Number: DERL-02 | Start Date*: 2010-02-01 |
| Sponsor Name:Dermal Laboratories Ltd | ||
| Full Title: A study to determine the effects on stratum corneum of a clinical hand cleansing protocol comparing two antiseptic hand washes, using non-invasive instrumental methods in human volunteers. | ||
| Medical condition: No medical condition is to be investigated, as such. We are looking to avoid occupational hand dermatitis in healthcare professionals, simulated using a repeat hand wash cleansing protocol in heal... | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: GB (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2006-005953-31 | Sponsor Protocol Number: STAB 1 | Start Date*: 2007-05-03 |
| Sponsor Name:GlaxoSmithKline Consumer Healthcare GmbH & Co. KG | ||
| Full Title: Inhibition of Dental Plaque Regrowth by an Ethanol-Free 0,2% Chlorhexidine Mouth Rinsing Solution | ||
| Medical condition: The purpose of this study is to examine the inhibitory effect of an ethanol-free 0,2% chlorhexidine digluconate (CHX) mouthrinse on the bacterial plaque growth after professional tooth cleaning in ... | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: DE (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2008-000333-22 | Sponsor Protocol Number: DERL-01 | Start Date*: 2008-04-30 |
| Sponsor Name:Dermal Laboratories Ltd | ||
| Full Title: A study to compare the effects on stratum corneum of two medical hand wash formulations, using non-invasive instrumental methods in human volunteers. | ||
| Medical condition: The study is a healthy volunteer study. | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: GB (Completed) | ||
| Trial results: View results | ||
| 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: 2013-005521-23 | Sponsor Protocol Number: QUAMED13 | Start Date*: 2014-06-19 | ||||||||||||||||
| Sponsor Name:QUALIPHAR NV | ||||||||||||||||||
| Full Title: Efficacy and safety assessment of Chlorhexidine hydrochloride - Lidocaine hydrochloride (MEDICA ®) versus placebo in adult patients with sore throat and/or acute pharyngitis | ||||||||||||||||||
| Medical condition: Sore throat or acute pharyngitis | ||||||||||||||||||
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| Population Age: Adults | Gender: Male, Female | |||||||||||||||||
| Trial protocol: DK (Completed) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
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