- Trials with a EudraCT protocol (37)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
37 result(s) found for: Duodenum.
Displaying page 1 of 2.
| EudraCT Number: 2016-002897-10 | Sponsor Protocol Number: DDD16JRcdk | Start Date*: 2016-09-14 |
| Sponsor Name:KU Leuven - Drug Delivery and Disposition | ||
| Full Title: Determination of free concentrations of paracetamol, amxocilline and valsartan in the duodenum by using a capillary diffusion catheter | ||
| Medical condition: Healthy human volunteers, investigation of free drug concentrations in the duodenum | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: BE (Prematurely Ended) | ||
| Trial results: View results | ||
| EudraCT Number: 2020-005747-23 | Sponsor Protocol Number: 10 | Start Date*: 2021-05-05 |
| Sponsor Name:Nemocnice Agel Ostrava-Vítkovice a.s. | ||
| Full Title: Use of mucolytic solution before gastroscopy, double-blind, randomized study | ||
| Medical condition: Visibility mucosal score during upper endoscopy after administration of mucolytic solution | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: CZ (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2020-004168-24 | Sponsor Protocol Number: BETHESDaCD | Start Date*: 2023-12-29 | |||||||||||
| Sponsor Name:Medical University of Warsaw | |||||||||||||
| Full Title: Evaluation of the efficacy of topical treatment with budesonide in children with Crohn's disease located in the esophagus and/or stomach and/or duodenum - BETHESDa | |||||||||||||
| Medical condition: Crohn's disease | |||||||||||||
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| Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: PL (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2021-000085-14 | Sponsor Protocol Number: D3258C00001 | Start Date*: Information not available in EudraCT | ||||||||||||||||
| Sponsor Name:AstraZeneca AB | ||||||||||||||||||
| Full Title: A Multi-center, Randomized, Double-blind, Parallel-group, Placebo-controlled 3-Part Phase 3 Study to Demonstrate the Efficacy and Safety of Benralizumab in Patients with Eosinophilic Gastritis and/... | ||||||||||||||||||
| Medical condition: Eosinophilic Gastritis and/or Gastroenteritis | ||||||||||||||||||
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| Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: DE (Completed) ES (Ongoing) NL (Completed) PL (Completed) IT (Completed) FR (Completed) BE (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2012-005387-10 | Sponsor Protocol Number: ERY-PAO | Start Date*: 2013-03-27 |
| Sponsor Name:Department of hospital Pharmacy, Medical Centre Haaglanden | ||
| Full Title: Effect of Roux-en-Y gstric bypass surgery in morbidly obese patients on Pharmacokinetics of (Acetyl)salicylic acid and Omeprazole. | ||
| Medical condition: Roux-en-Y gastric bypass (RYGB) surgery is a successful treatment for morbid obesity. In this procedure, a small gastric pouch is created. The duodenum is bypassed by connecting the jejunum to this... | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: NL (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2005-002349-38 | Sponsor Protocol Number: 2-54-52030-156 | Start Date*: 2007-02-26 |
| Sponsor Name:Beaufour Ipsen Pharma-Ipsen Biotech Department | ||
| Full Title: Phase III multicentre, Randomised, Double Blind, Comparative study to assess the efficacy and safety of lanreotide 30mg versus placebo as a palliative treatment of clinical symptoms associated with... | ||
| Medical condition: Patient having a high digestive obstruction of malignant origin i.e. located on the upper part of the gastro-intestinal tract (stomach, duodenum, small bowel) for whom surgery is inappropriate. | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: NL (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2006-002803-15 | Sponsor Protocol Number: 12096 | Start Date*: 2006-08-18 | |||||||||||
| Sponsor Name:Aarhus Sygehus | |||||||||||||
| Full Title: Bioavailability, Pharmacokinetics and Pharmacodynamics of Insulin Aspart administered in the Duodenum in healthy volunteers – an open single blinded and uncontrolled exploratory trial | |||||||||||||
| Medical condition: Diabetes Mellitus | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: DK (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2022-000849-32 | Sponsor Protocol Number: 1/2022 | Start Date*: 2022-05-10 |
| Sponsor Name:Helsinki University Hospital | ||
| Full Title: The effect of tenofovir disoproxil fumarate (TDF) versus tenofovir alafenamide (TAF) on proximal small intestine – a potential mechanism to explain opposing effects on body weight | ||
| Medical condition: HIV-positive people who have good and stable treatment response for HIV-medication which includes either tenofovir disoproxil (TDF) or tenoforvir alafenamide (TAF) | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: FI (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2015-000244-42 | Sponsor Protocol Number: acid_permeability_healthyvolunteers | Start Date*: 2015-04-21 | |||||||||||
| Sponsor Name:KU Leuven | |||||||||||||
| Full Title: The role of mast cells on duodenal permeability after duodenal acid perfusion in healthy volunteers | |||||||||||||
| Medical condition: To investigate the role of mast cells on duodenal permeability after duodenal acid perfusion. The study will be done in healthy volunteers and the results will give an indication about the role of ... | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: BE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2009-014886-21 | Sponsor Protocol Number: BA_BICG_UMCG_1 | Start Date*: 2010-01-26 |
| Sponsor Name:University Medical Centre Groningen | ||
| Full Title: Intraoperative bile duct visualisation in children with biliary atresia using a fluorescence camera system: a pilot study | ||
| Medical condition: Biliary atresia | ||
| Disease: | ||
| Population Age: Newborns, Infants and toddlers, Under 18 | Gender: Male, Female | |
| Trial protocol: NL (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2012-000427-41 | Sponsor Protocol Number: CPPFAP-310 | Start Date*: 2014-05-15 |
| Sponsor Name:Cancer Prevention Pharmaceuticals, Inc. | ||
| Full Title: A Double-Blind, Randomized, Phase III Trial of the Safety and Efficacy of CPP-1X/Sulindac Compared With CPP-1X, Sulindac as Single Agents in Patients with Familial Adenomatous Polyposis (FAP) | ||
| Medical condition: Familial Adenomatous Polyposis (FAP) | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: GB (Completed) DE (Completed) NL (Completed) ES (Completed) BE (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2015-002209-12 | Sponsor Protocol Number: ABR59689 | Start Date*: 2017-06-21 | |||||||||||||||||||||||||||||||||||||||||
| Sponsor Name:Erasmus MC-Sophia Children's Hospital | |||||||||||||||||||||||||||||||||||||||||||
| Full Title: Less opioids after major abdominal surgery in young infants using wound catheter infusion with local anesthetics: a randomized controlled trial. | |||||||||||||||||||||||||||||||||||||||||||
| Medical condition: Children < 1 year of age undergoing major open abdominal surgery. | |||||||||||||||||||||||||||||||||||||||||||
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| Population Age: Preterm newborn infants, Newborns, Infants and toddlers, Under 18 | Gender: Male, Female | ||||||||||||||||||||||||||||||||||||||||||
| Trial protocol: NL (Prematurely Ended) | |||||||||||||||||||||||||||||||||||||||||||
| Trial results: View results | |||||||||||||||||||||||||||||||||||||||||||
| EudraCT Number: 2008-007348-32 | Sponsor Protocol Number: CSOM230D2203 | Start Date*: 2009-05-06 | |||||||||||
| Sponsor Name:Novartis Pharma Services AG | |||||||||||||
| Full Title: An open label, multicenter, single arm study of pasireotide LAR in patients with rare tumors of neuroendocrine origin | |||||||||||||
| Medical condition: The following tumors are included: 1. NETs of the pancreas or duodenum: Insulinoma, Gastrinoma, VIPoma, glucagonoma, 2. Pituitary NETs: Thyrotropic-pituitary adenoma (TSH), Gonadotropic adenoma, Pr... | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Completed) DE (Completed) IT (Completed) ES (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2012-005528-13 | Sponsor Protocol Number: 30112012 | Start Date*: 2014-06-17 | |||||||||||
| Sponsor Name:Helsinki University Hospital | |||||||||||||
| Full Title: Comparison of Novel Articaine Lozenge Versus Placebo for Upper Gastrointestinal Endoscopy in Adults. A Randomized Double-blinded Controlled Study | |||||||||||||
| Medical condition: Patients who undergo esophagogastroduodenoscopy procedure for a first time | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FI (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2009-012260-14 | Sponsor Protocol Number: 20050418 | Start Date*: 2010-08-27 |
| Sponsor Name:Department of Endocrine Oncology | ||
| Full Title: An open, non-randomized phase-2 study of efficacy and safety of treatment with 177Lutetium-DOTA0-Tyr3-octreotate in patients with neuroendocrine tumors | ||
| Medical condition: Patients with malignant neuroendocrine tumours, not amenable to surgical treatment or radiofrequency ablation. Renal, bone marrow and liver function must be sufficient. | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: SE (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2008-001886-26 | Sponsor Protocol Number: TRI-002-INT | Start Date*: 2010-06-29 |
| Sponsor Name:GALENICA S.A. | ||
| Full Title: A multicenter, double-blind, randomized, placebo controlled phase III study of the efficacy and safety of Trimebutine 300 mg twice daily for the relief of functional dyspeptic patients | ||
| Medical condition: | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: GR (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2017-004248-39 | Sponsor Protocol Number: PPI-microbiome | Start Date*: 2018-01-04 |
| Sponsor Name:TARGID, KU Leuven | ||
| Full Title: Effect of Proton Pump Inhibitors on the duodenal microbiome in healthy volunteers | ||
| Medical condition: We will assess the effect of Proton Pump Inhibitors (PPI) on the duodenal, oral and fecal microbiota composition in healthy volunteers | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: BE (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2017-004355-23 | Sponsor Protocol Number: PPI-microbiome-FD | Start Date*: 2018-01-04 |
| Sponsor Name:TARGID, KU Leuven | ||
| Full Title: Effect of Proton Pump Inhibitors on the duodenal microbiome in Functional Dyspepsia patients | ||
| Medical condition: Functional Dyspepsia (FD) | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: BE (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2006-002275-40 | Sponsor Protocol Number: 2006-002275-40 | Start Date*: 2007-01-24 |
| Sponsor Name:Uppsala University Hospital, Dept. of Medical Sciences | ||
| Full Title: Prospective study of patients treated with pegylated interferon-alpha 2b (PegIntron) for metastasizing ileal/coecal carcinoids | ||
| Medical condition: Metastasizing ileal/coecal carcinoids (WHO ICD-10 code: C17.9) | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: SE (Prematurely Ended) DK (Prematurely Ended) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2018-000242-19 | Sponsor Protocol Number: RHMGSU0241 | Start Date*: 2018-04-13 | |||||||||||
| Sponsor Name:University Hospitals Southampton NHS Trust | |||||||||||||
| Full Title: Change in nutritional state and postoperative outcome following preoperative introduction of nutritional supplements and pancreatic enzymes in patients undergoing Whipple’s procedure for pancreatic... | |||||||||||||
| Medical condition: Patients undergoing Whipple’s procedure for pancreatic head tumours | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
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