- Trials with a EudraCT protocol (43)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (798)
43 result(s) found for: Stoma.
Displaying page 1 of 3.
EudraCT Number: 2018-000876-14 | Sponsor Protocol Number: ACO/ARO/AIO-18.1 | Start Date*: 2020-01-21 | ||||||||||||||||
Sponsor Name:University Hospital Frankfurt, Goethe University | ||||||||||||||||||
Full Title: ACO/ARO/AIO-18.1: Short-course radiotherapy versus chemoradiotherapy, followed by consolidation chemotherapy, and selective organ preservation for MRI-defined intermediate and high-risk rectal canc... | ||||||||||||||||||
Medical condition: Locally advanced rectal cancer (UICC stage II and III) | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Trial now transitioned) | ||||||||||||||||||
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: 2021-002588-23 | Sponsor Protocol Number: 2019/0407/HP | Start Date*: 2023-03-13 | ||||||||||||||||
Sponsor Name:CHU de Rouen | ||||||||||||||||||
Full Title: Neoadjuvant Chemotherapy for Obstructive Colon cancER first Treated by cOlostomy: A randomized phase III trial - COnCERTO (French 01-18) | ||||||||||||||||||
Medical condition: Patients first treated by stoma and requiring chemotherapy for obstructive colon cancer | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: FR (Trial now transitioned) | ||||||||||||||||||
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: 2013-005499-16 | Sponsor Protocol Number: 2013-624 | Start Date*: 2014-01-31 | |||||||||||||||||||||
Sponsor Name:Rigshospitalet, 2121 | |||||||||||||||||||||||
Full Title: Pilot Study with Treatment of Short Bowel Syndrome Patients with end-jejunostomi with the Glucagon-Like Peptide-1 analogue, Liraglutide (Victoza®) | |||||||||||||||||||||||
Medical condition: Short Bowel Syndrome with intestinal failure (SBS IF) | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: DK (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2014-004707-67 | Sponsor Protocol Number: 2014-880 | Start Date*: 2016-01-13 | ||||||||||||||||
Sponsor Name:Hospices Civils de Lyon | ||||||||||||||||||
Full Title: REDUCTION BY PASIREOTIDE OF THE EFFLUENT VOLUME IN HIGH-OUTPUT ENTEROSTOMY IN PATIENTS REFRACTORY TO USUAL MEDICAL TREATMENT: PHASE II MULTICENTRIC RANDOMIZED DOUBLE BLIND PLACEBO CONTROLLED STUDY | ||||||||||||||||||
Medical condition: Patients with high-output ileostomy or jejunostomy and failure of treatment with loperamide +/- codein syrup | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: FR (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-001202-32 | Sponsor Protocol Number: TA799-007 | Start Date*: 2020-11-02 | |||||||||||
Sponsor Name:VectivBio AG | |||||||||||||
Full Title: A multicenter, double-blind, randomized, placebo-controlled trial to evaluate the efficacy and safety of apraglutide in adult subjects with short bowel syndrome and intestinal failure (SBS-IF) | |||||||||||||
Medical condition: short bowel syndrome and intestinal failure | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) CZ (Completed) FR (Completed) NO (Completed) BE (Completed) HU (Completed) PL (Completed) SE (Completed) DK (Completed) IT (Completed) ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-001778-12 | Sponsor Protocol Number: HUGTP-CIR-FIBRIN-GLUE-01 | Start Date*: 2019-04-15 | |||||||||||||||||||||
Sponsor Name:Fundació Institut de Recerca en Ciències de la Salut Germans Trias i Pujol | |||||||||||||||||||||||
Full Title: USE OF A FIBRINE ADHESIVE TO REDUCE THE DEHISCENCE OF ESOFAGOYEYUNAL ANASTOMOSIS IN TOTAL GASTRECTOMIES BY CANCER: RANDOMIZED AND MULTICENTRIC STUDY. | |||||||||||||||||||||||
Medical condition: The dehiscence of the esophagojejunal anastomosis after a total gastrectomy in patients with gastric adenocarcinoma | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||||||||||||
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: 2015-000825-35 | Sponsor Protocol Number: U1111-1167-2731 | Start Date*: 2015-08-27 | |||||||||||
Sponsor Name:Rigshospitalet Blegdamsvej | |||||||||||||
Full Title: The effect of the glucagon-like peptide-1 analogue, liraglutide (Victoza®), on jejunostomy output and intestinal absorption in short bowel syndrome patients, a double-blind cross-over study | |||||||||||||
Medical condition: Short bowel syndrome (SBS) is a clinical situation with reduced absorptive mucosal surface due to extensive surgical resection. SBS leads to increased intestinal losses of fluids and electrolytes; ... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
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: 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: 2017-000732-34 | Sponsor Protocol Number: ABOXY_2017 | Start Date*: 2017-06-21 | ||||||||||||||||||||||||||
Sponsor Name:Mech-Sense, Dept. Gastroenterology & Hepatology, Aalborg University Hospital | ||||||||||||||||||||||||||||
Full Title: Oral Controlled Release Formulations to Patients with Gastrointestinal Dysfunction – Is the Release of Drug and the Absorption Impaired? | ||||||||||||||||||||||||||||
Medical condition: Healthy (pain) and patients (pain). | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: DK (Prematurely Ended) | ||||||||||||||||||||||||||||
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: 2006-002385-20 | Sponsor Protocol Number: CAO/ARO/AIO-04 | Start Date*: 2006-06-28 | |||||||||||
Sponsor Name:Strahlenklinik, Universitätsklinikum Erlangen, insoweit handelnd für den Freistaat Bayern | |||||||||||||
Full Title: Prospective randomised multicenter phase-III-study: Preoperative radiochemotherapy and adjuvant chemotherapy with 5-Fluorouracil plus oxaliplatin versus preoperative radiochemotherapy and adjuvant... | |||||||||||||
Medical condition: Male or femal patients suffering from histologically proven carcinoma of the rectum (tumor ≤ 12cm from the anal verge, with clinically staged T3/4 or any node-positive disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: (No results available) |
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