- Trials with a EudraCT protocol (61)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (9)
61 result(s) found for: Washing.
Displaying page 1 of 4.
EudraCT Number: 2019-002856-18 | Sponsor Protocol Number: Mannitol_03-2018 | Start Date*: 2020-06-04 | |||||||||||
Sponsor Name:NTC s.r.l. | |||||||||||||
Full Title: Efficacy and Safety of mAnniTol in bowel preparation: assessment of adequacy and presence of Intestinal levelS of hydrogen and methane during elective colonoscopy aFter mAnnitol or standard split 2... | |||||||||||||
Medical condition: Subjects scheduled for elective colonoscopy to be prepared and performed according to ESGE (European Society of Gastrointestinal Endoscopy - ESGE) guidelines. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) DE (Completed) IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-005688-26 | Sponsor Protocol Number: Abstral | Start Date*: 2012-02-01 | |||||||||||
Sponsor Name:Turku University Hospital | |||||||||||||
Full Title: Procedural pain treatment with transmucosal sublingual fentanyl tablet in colonoscopy patients | |||||||||||||
Medical condition: Patients undergoing colonoscopy | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-002192-40 | Sponsor Protocol Number: periodld001 | Start Date*: 2006-07-13 |
Sponsor Name:Zsolt Lohinai DMD PhD | ||
Full Title: New treatment of periodontitis by inhibition of lysine decarboxilase enzyme | ||
Medical condition: healthy volunteers | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: HU (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2009-014845-95 | Sponsor Protocol Number: NRL0706-01/2009 (VOM) | Start Date*: 2010-02-22 | |||||||||||
Sponsor Name:Norgine Ltd. | |||||||||||||
Full Title: Open study to assess the tolerability, safety and efficacy of an adapted 2 litre gut cleansing solution (NRL0706) in routine colon cleansing prior to colonoscopies for colon tumour screening | |||||||||||||
Medical condition: Subjects without relevant clinical symptoms for gastrointestinal disorders will undergo a complete selective colonoscopy for colon cancer screening. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-005575-34 | Sponsor Protocol Number: P060240 | Start Date*: 2008-02-08 | |||||||||||
Sponsor Name:ASSISTANCE PUBLIQUE - HOPITAUX DE PARIS (AP-HP) | |||||||||||||
Full Title: Comparaison de la tolérance et de l'acceptabilité de la coloscopie sous sédation par mélange équimolaire d'oxygène et de protoxyde d'azote par rapport à l'anesthésie générale : Etude randomisée mul... | |||||||||||||
Medical condition: maladies digestives. | |||||||||||||
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Population Age: Adults, Elderly | Gender: | ||||||||||||
Trial protocol: FR (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-022967-37 | Sponsor Protocol Number: IEOS570/510 | Start Date*: 2011-03-15 | |||||||||||
Sponsor Name:ISTITUTO EUROPEO DI ONCOLOGIA | |||||||||||||
Full Title: Bowel cleansing for colonoscopy: comparison between a same day low-volume preparation and a conventional split one. | |||||||||||||
Medical condition: Patients with indications to undergoing a complete colonoscopy | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-000869-36 | Sponsor Protocol Number: CSPT-END-DIG-2012 | Start Date*: 2013-06-28 | |||||||||||
Sponsor Name:Fundació Parc Taulí | |||||||||||||
Full Title: Multidisciplinary approach versus conventional approach in colonic preparation of hospitalized patients. A randomized controlled trial | |||||||||||||
Medical condition: Colon preparation for colonoscopy | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-003342-33 | Sponsor Protocol Number: STH16359 | Start Date*: 2012-09-28 | |||||||||||
Sponsor Name:Sheffield Teaching Hospitals NHS Foundation Trust | |||||||||||||
Full Title: Optimising the use of Entonox during screening colonoscopy: an open randomised controlled trial | |||||||||||||
Medical condition: Colonoscopy | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-002364-25 | Sponsor Protocol Number: NOR-01/2011(PDR) | Start Date*: 2011-10-31 | |||||||||||
Sponsor Name:Norgine Limited | |||||||||||||
Full Title: A multi-centre, randomised, investigator-blinded study comparing the polyp detection rate of two different types of bowel preparation: a 2-litre solution (MOVIPREP®) versus a hyperosmotic and stimu... | |||||||||||||
Medical condition: Patients with clinical symptoms or polyp history scheduled for either a diagnostic/surveillance colonoscopy or for a screening procedure in patients with a personal or familial risk of colon neopla... | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-001154-26 | Sponsor Protocol Number: FIBHNJ-2019-01 | Start Date*: 2019-08-01 |
Sponsor Name:Fundación de Investigación Biomédica Hospital Niño Jesús | ||
Full Title: Feasibility clinical trial of the combination of AloCelyvir with chemotherapy and radiotherapy for the treatment of children and adolescents with relapsed or refractory extracranial solid tumors. | ||
Medical condition: Relapsed or refractory extracranial solid tumors in children and adolescents. | ||
Disease: | ||
Population Age: Infants and toddlers, Children, Adolescents, Under 18, Adults | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2010-023643-15 | Sponsor Protocol Number: BUSCOPAN_PDR1 | Start Date*: 2011-01-18 | |||||||||||||||||||||
Sponsor Name:Deventer Hospital | |||||||||||||||||||||||
Full Title: The influence of hyoscine N-butylbromide on colonoscopic polyp detection ratio | |||||||||||||||||||||||
Medical condition: It is investigated whether the administration of Buscopan will improve the detection, removal and harvesting of colonic polyps during colonoscopy. | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: NL (Ongoing) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-001620-20 | Sponsor Protocol Number: CF13.01 | Start Date*: 2013-07-29 | |||||||||||
Sponsor Name:Laboratorios Casen-Fleet S.L.U. | |||||||||||||
Full Title: Randomized, multicentre, single blind study to evaluate the effectiveness of two administration schedules of CitraFleet (sodium picosulfate plus magnesium citrate) to cleanse the colon | |||||||||||||
Medical condition: Cleansing of colon | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-001026-16 | Sponsor Protocol Number: DELP-05 | Start Date*: 2015-04-01 | |||||||||||
Sponsor Name:Dermal Laboratories Limited | |||||||||||||
Full Title: Randomised, double-blind, bilateral comparison of two emollients in patients with dry skin | |||||||||||||
Medical condition: Dry eczematous skin | |||||||||||||
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Population Age: Adolescents, Under 18, Adults | Gender: Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-004206-25 | Sponsor Protocol Number: 1839IL/0711 | Start Date*: 2005-03-02 |
Sponsor Name:AstraZeneca AB | ||
Full Title: A PHASE II MULTICENTRE RANDOMISED, PARALLEL GROUP, DOUBLE-BLIND, PLACEBO-CONTROLLED STUDY OF ZD1839 (IRESSA TM) (250MG TABLET) PLUS BEST SUPPORTIVE CARE (BSC) VERSUS PLACEBO PLUS BSC IN CHEMOTHERAP... | ||
Medical condition: Non-Small Cell Lung Cancer | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: IE (Completed) CZ (Completed) | ||
Trial results: View results |
EudraCT Number: 2013-000634-35 | Sponsor Protocol Number: CB-17-01/08 | Start Date*: 2013-05-11 | |||||||||||
Sponsor Name:Cosmo Technologies Ltd. | |||||||||||||
Full Title: Effect of oral administration of Methylene Blue MMX® tablets on double-stranded DNA damage assessed by γH2AX analysis of colon biopsy samples | |||||||||||||
Medical condition: Out-patients of both sexes scheduled for a screening or surveillance colonoscopy and identified as having the clinical requirement for a second colonoscopy within 2 weeks of the initial colonoscopy. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-002799-15 | Sponsor Protocol Number: INTERPRET | Start Date*: 2020-09-16 | |||||||||||
Sponsor Name:ALMA MATER STUDIORUM UNIVERSITà DI BOLOGNA | |||||||||||||
Full Title: Efficacy of a very low-volume Polyethylene Glycole (PEG 1L) bowel preparation vs. low-volume (2L) and high-volume (4L) PEG-based preparations. A randomized controlled study. | |||||||||||||
Medical condition: Adult in hospital patients who undergo colonoscopy for any medical disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-013400-31 | Sponsor Protocol Number: STEADI-09 | Start Date*: 2010-08-10 |
Sponsor Name:University of Southampton | ||
Full Title: A phase 2, double-blind, placebo-controlled study of the safety and tolerability of etanercept in patients with Alzheimer’s disease | ||
Medical condition: Alzheimer's disease | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2009-014550-14 | Sponsor Protocol Number: DPSI-Acanya-P4-02 / 290622BS | Start Date*: 2009-09-25 |
Sponsor Name:Dow Pharmaceutical Sciences, Inc on behalf of Coria Laboratories | ||
Full Title: A single center, randomized, controlled study to determine the irritant potential of topical acne formulations on intact healthy skin on the back following repeated application during a 21-day trea... | ||
Medical condition: Cumulative irritation test | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2012-001789-13 | Sponsor Protocol Number: QUINA/2012 | Start Date*: 2012-11-16 |
Sponsor Name:Instituto de Investigacion Sanitaria La e | ||
Full Title: Double-blind, randomized, controlled contraceptives, parallel group, to assess the effect on nerve fibers in patients diagnosed with endometriosis grade III / IV symptomatic ascending-dose oral qui... | ||
Medical condition: Endometriosis grade III/IV | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2009-012194-35 | Sponsor Protocol Number: 290404BS | Start Date*: 2009-12-22 |
Sponsor Name:bioskin GmbH | ||
Full Title: A single-center, randomized, controlled, observer-blind, phase IV study to develop the atopic localized eczema regression test (ALERT) using marketed topical corticosteroid formulations of differen... | ||
Medical condition: Patients with a pre-disposition for Atopic Dermatitis | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: View results |
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