- Trials with a EudraCT protocol (86)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
86 result(s) found for: Therapeutic endoscopy.
Displaying page 3 of 5.
EudraCT Number: 2014-003262-25 | Sponsor Protocol Number: MK8259-022 | Start Date*: 2014-12-12 | |||||||||||
Sponsor Name:Merck Sharp & Dohme Corp., a subsidiary of Merck & Co., Inc. | |||||||||||||
Full Title: An open label, single group assignment design study to correlate soluble ST2 with clinical, endoscopic and histological activity in moderate to severe Ulcerative Colitis patients under golimumab | |||||||||||||
Medical condition: Ulcerative Colitis | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: PT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-022759-42 | Sponsor Protocol Number: CNTO1275CRD3002 | Start Date*: 2011-08-29 | |||||||||||
Sponsor Name:Janssen-Cilag International N.V. | |||||||||||||
Full Title: A Phase 3, Randomized, Double-blind, Placebo-controlled, Parallel-group, Multicenter Study to Evaluate the Safety and Efficacy of Ustekinumab Induction Therapy in Subjects with Moderately to Severe... | |||||||||||||
Medical condition: Moderately to severely active Crohn's disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) GB (Completed) BE (Completed) ES (Completed) NL (Completed) HU (Completed) IS (Completed) BG (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-001216-31 | Sponsor Protocol Number: SAG-26/UCA | Start Date*: 2005-05-30 | |||||||||||
Sponsor Name:Dr. Falk Pharma GmbH | |||||||||||||
Full Title: Double-blind, double-dummy, randomised, multicentre, comparative study of the efficacy and tolerability of once daily 3.0 g mesalazine granules versus three times daily 1.0 g mesalazine granules in... | |||||||||||||
Medical condition: Therapy of active ulcerative colitis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) LT (Completed) SK (Completed) HU (Completed) LV (Completed) CZ (Completed) EE (Completed) SI (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-003669-17 | Sponsor Protocol Number: NEOPA | Start Date*: 2013-12-17 | |||||||||||
Sponsor Name:University Medical Center Hamburg-Eppendorf | |||||||||||||
Full Title: Sequential neoadjuvant chemoradiotherapy (CRT) followed by curative surgery vs. primary surgery alone for resectable, non-metastasized pancreatic adenocarcinoma (NEOPA). | |||||||||||||
Medical condition: Non-metastasized, adenocarcinoma of the pancreatic head/uncinate process or body of pancreas that was treated with extended pancreatic head/body resection larger than 2 cm in size (≥cT2) and/or in ... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-004217-26 | Sponsor Protocol Number: CSUC-01/16 | Start Date*: 2017-04-21 |
Sponsor Name:InDex Pharmaceuticals AB | ||
Full Title: A Randomised Dose-Optimisation Study to Evaluate the Efficacy and Safety of Cobitolimod in Moderate to Severe Active Ulcerative Colitis Patients | ||
Medical condition: Moderate to Severe left-sided Active Ulcerative Colitis | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) HU (Completed) SE (Completed) ES (Completed) CZ (Completed) FR (Completed) IT (Completed) | ||
Trial results: View results |
EudraCT Number: 2004-001218-15 | Sponsor Protocol Number: SAG-27/UCR | Start Date*: 2005-04-04 |
Sponsor Name:Dr. Falk Pharma GmbH | ||
Full Title: Double-blind, double-dummy, randomised, multicentre, 12-months, comparative study of the efficacy and tolerability of once daily 3.0 g mesalazine granules versus once daily 1.5 g mesalazine granule... | ||
Medical condition: Maintenance therapy of ulcerative colitis | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) LT (Completed) SK (Completed) HU (Completed) EE (Completed) LV (Completed) SI (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: 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: 2019-004090-50 | Sponsor Protocol Number: CT-OST-122-02 | Start Date*: 2020-02-07 |
Sponsor Name:ONCOSTELLAE S.L. | ||
Full Title: A Phase Ib/IIa, randomized, double blind, placebo controlled, multicenter clinical trial to evaluate the safety, pharmacokinetics and efficacy of oral treatment with OST-122 in patients with modera... | ||
Medical condition: Moderate to severe ulcerative colitis | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2013-004475-13 | Sponsor Protocol Number: 13.031 | Start Date*: 2014-03-05 | |||||||||||
Sponsor Name:Fredericia Hospital | |||||||||||||
Full Title: Pharmacological relaxation of the ureter when using access sheaths during ureterorenoscopy | |||||||||||||
Medical condition: Resistance in the ureter when inserting a ureteral access sheath during ureterorenoscopy. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-002691-14 | Sponsor Protocol Number: RC2019.1.6_ROSSI | Start Date*: 2019-10-30 | |||||||||||
Sponsor Name:IRCCS, OSPEDALE PEDIATRICO BAMBINO GESÙ DI ROMA | |||||||||||||
Full Title: VISCOUS BUDESONIDE IN PATIENTS AFFECTED BY EOSINOPHILIC ESOPHAGITIS, OPERATED FOR ESOPHAGEAL ATRESIA | |||||||||||||
Medical condition: Eosinophilicesophagitis (EoE) in Esophageal atresia (EA). | |||||||||||||
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Population Age: Newborns, Infants and toddlers, Children, Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
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: 2013-005065-38 | Sponsor Protocol Number: ECHI-TS-2 | Start Date*: 2014-02-17 |
Sponsor Name:Medizinische Universität Innsbruck, Universitätsklinik für Innere Medizin I | ||
Full Title: Concentrations of echinocandins in ascites, pleural effusion, bile, wound secretion and cerebrospinal fluid – a pilot study | ||
Medical condition: Invasive fungal infection treated with an echinocandin and indication for paracentesis, thoracentesis, bile deviation or sampling, lumbar puncture or VAC therapy | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2018-003594-95 | Sponsor Protocol Number: MTXSB2018 | Start Date*: 2019-04-30 | ||||||||||||||||
Sponsor Name:Amsterdam UMC location AMC | ||||||||||||||||||
Full Title: Methotrexate to suppress immunogenicity to anti-tumor necrosis factor therapy in IBD patients with loss of response | ||||||||||||||||||
Medical condition: Inflammatory bowel disease: Crohn's disease and Ulcerative colitis | ||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: NL (Ongoing) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2022-001107-41 | Sponsor Protocol Number: IMIB-BICOV-2022-01 | Start Date*: 2022-07-21 | ||||||||||||||||
Sponsor Name:Fundación para la Formación e Investigación Sanitarias de la Región de Murcia (FFIS) | ||||||||||||||||||
Full Title: Combined treatment of intraperitoneal chemotherapy after optimal interval surgery in advanced ovarian cancer | ||||||||||||||||||
Medical condition: Ovarian cancer (OV-1) | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Female | |||||||||||||||||
Trial protocol: ES (Ongoing) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-004313-15 | Sponsor Protocol Number: NI-0401-01 | Start Date*: 2006-07-14 |
Sponsor Name:NovImmune S.A. | ||
Full Title: A Phase I/IIa, Double-blind, Randomized, Placebo-controlled, Dose-Escalation Study of NI-0401 in Patients with Moderate to Severe Active Crohn´s Disease | ||
Medical condition: Moderate to Severe Active Crohn´s Disease | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Completed) GB (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2007-001200-20 | Sponsor Protocol Number: CSET 1287 | Start Date*: 2007-06-01 |
Sponsor Name:Institut Gustave Roussy | ||
Full Title: A Multicenter, Randomized Phase II Trial Assessing the Activity of Gemcitabine – Oxaliplatin Chemotherapy Alone or in Combination with Cetuximab in Patients with Advanced Biliary Cancer | ||
Medical condition: adenocarcinoma of the biliary tract ( gallbladder, intra and/ or extrahepatic bile ducts, ampulla of Vater) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FR (Ongoing) DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2009-011608-51 | Sponsor Protocol Number: MCA111407 | Start Date*: 2009-08-17 | |||||||||||
Sponsor Name:GlaxoSmithKline Research and Development Ltd | |||||||||||||
Full Title: A Double-Blind, Double-Dummy, Placebo- and Active-Controlled Dose Escalation Study to Evaluate the Safety, Tolerability, Pharmacokinetics and Anti-Inflammatory Effects of GSK1399686 in Patients wit... | |||||||||||||
Medical condition: Ulcerative colitis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) BE (Completed) DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2023-000171-13 | Sponsor Protocol Number: P23 | Start Date*: 2023-08-23 | ||||||||||||||||
Sponsor Name:leiden university medical center | ||||||||||||||||||
Full Title: SGM-101 tumor-targeted fluorescence endoscopy to enable discrimination of malignant from benign tissue in rectal polyps with suspected T1 adenocarcinoma or high grade dysplasia: a feasibility study | ||||||||||||||||||
Medical condition: Early rectal cancer/ big polyps with suspected T1 rectal cancer. | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: NL (Trial now transitioned) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-004223-16 | Sponsor Protocol Number: PEBBLE | Start Date*: 2021-05-10 | |||||||||||
Sponsor Name:Queen Mary University of London | |||||||||||||
Full Title: A phase II study investigating preoperative bintrafusp alfa in operable urothelial carcinoma of the bladder. | |||||||||||||
Medical condition: Urothelial carcinoma requiring radical cystectomy with bilateral pelvic lymph node dissection | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Prematurely Ended) | |||||||||||||
Trial results: View results |
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