- Trials with a EudraCT protocol (34)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
34 result(s) found for: Gastrointestinal motility.
Displaying page 1 of 2.
EudraCT Number: 2014-002239-33 | Sponsor Protocol Number: CRHMOT2014 | Start Date*: 2014-10-14 |
Sponsor Name:TARGID, KU Leuven | ||
Full Title: The effect of corticotrophin-releasing hormone (CRH) on esophageal motility in healthy volunteers | ||
Medical condition: Changes in esophageal motility induced by CRH-administration | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: View results |
EudraCT Number: 2019-000959-14 | Sponsor Protocol Number: 29BRC18.0262 | Start Date*: 2021-03-16 | |||||||||||||||||||||
Sponsor Name:CHRU de Brest | |||||||||||||||||||||||
Full Title: The NIPA study: A randomized double-blind control clinical trial Naloxegol administration to prevent opioids induced gastrointestinal motility disturbance in brain Injured PAtients. | |||||||||||||||||||||||
Medical condition: Prevent opioids induced gastrointestinal motility disturbance in brain Injured Patients. | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: FR (Trial now transitioned) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-005043-16 | Sponsor Protocol Number: DDD17FPV | Start Date*: 2020-02-18 |
Sponsor Name:KU Leuven - Drug Delivery and Disposition | ||
Full Title: Impact of stomach motility on the gastrointestinal behavior of fosamprenavir in healthy volunteers | ||
Medical condition: Healthy volunteers | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: View results |
EudraCT Number: 2020-004180-13 | Sponsor Protocol Number: OCARINA | Start Date*: 2021-10-18 | ||||||||||||||||
Sponsor Name:KU Leuven | ||||||||||||||||||
Full Title: The effect of obeticholic acid on gut microbiota, gastric motility, accommodation, gastrointestinal peptide in healthy volunteers | ||||||||||||||||||
Medical condition: The study will focus on the underlying mechanisms of gastrointestinal motility and gut microbiota in healthy subjects. | ||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: BE (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-004600-35 | Sponsor Protocol Number: Modifast3 | Start Date*: 2012-12-19 |
Sponsor Name:KULeuven | ||
Full Title: Effect of diet-induced weight loss on motilin, ghrelin, bitter taste perception, hunger and the migrating motor complex: a prospective study | ||
Medical condition: Gastrointestinal contractility and hormones will be studied in obese patients before and after weight loss induced by a diet | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: BE (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2016-001439-11 | Sponsor Protocol Number: DDD16BICARBONATE | Start Date*: 2016-06-28 |
Sponsor Name:KU Leuven - Drug Delivery and Disposition | ||
Full Title: Influence of bicarbonate on drug gastrointestinal behaviour and disposition | ||
Medical condition: Healthy human volunteers (administration of an antipyretic, analgetic drug) | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: View results |
EudraCT Number: 2021-000854-24 | Sponsor Protocol Number: VE-CIP2001/2021 | Start Date*: 2021-12-21 | |||||||||||
Sponsor Name:ALFASIGMA S.P.A. | |||||||||||||
Full Title: Velusetrag for the treatment of Chronic Intestinal Pseudo-Obstruction (CIPO). A multicenter double-blind, placebo-controlled, cross-over, multiple (n=1) trial. | |||||||||||||
Medical condition: Chronic intestinal pseudo-obstruction (CIPO) is a rare, severe condition characterized by an impairment of coordinated propulsive activity in the intestinal tract resulting in a clinical picture si... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) BE (Completed) IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-004082-33 | Sponsor Protocol Number: erythstom2 | Start Date*: 2011-10-05 |
Sponsor Name:UZLeuven | ||
Full Title: The role of induced phase 3 contractions in the control of hunger and food intake | ||
Medical condition: Gastrointestinal contractility will be studied in healthy volunteers for 7 hours in a fasting condition | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: View results |
EudraCT Number: 2014-000361-52 | Sponsor Protocol Number: prucalopride/VNS1 | Start Date*: 2014-05-15 |
Sponsor Name:KULeuven | ||
Full Title: Pilot study: Anti-inflammatory effect of preoperative stimulation of the enteric nervous system: a potential new therapeutic intervention to shorten gastroparesis | ||
Medical condition: Patients undergoing pancreaduodenectomy due to benign or malignant tumor drug will be studied for prokinetic or anti-inflammatory effects, because they are known to influence gastrointestinal mo... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2020-002593-27 | Sponsor Protocol Number: S64291 | Start Date*: 2022-06-17 |
Sponsor Name:UZ Leuven | ||
Full Title: Budesonide as a treatment for low-grade duodenal inflammation in functional dyspepsia. | ||
Medical condition: Functional dyspepsia | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2012-003939-27 | Sponsor Protocol Number: 1-10-72-356-12 | Start Date*: 2013-02-12 | |||||||||||
Sponsor Name:Klaus Krogh | |||||||||||||
Full Title: Objective evaluation of the effects of pasireotide on gastrointestinal and colorectal transit times, rectal wall properties, and postprandial response in patients with carcinoid diarrhea | |||||||||||||
Medical condition: Patients with neuroendocrine tumors and carcinoid diarrhea | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-023228-26 | Sponsor Protocol Number: TZP-101-CL-P007 | Start Date*: 2011-02-18 | |||||||||||
Sponsor Name:Tranzyme, Inc. | |||||||||||||
Full Title: A Multicenter, Randomized, Double-Blind, Placebo-Controlled Study to Evaluate the Efficacy and Safety of Intravenous (IV) Ulimorelin Administered Post-Operatively to Accelerate Recovery of Gastroin... | |||||||||||||
Medical condition: post-operative ileus in subjects who have undergone partial bowel resection | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) GB (Completed) IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-004941-13 | Sponsor Protocol Number: SIEMI01 | Start Date*: 2007-12-07 |
Sponsor Name:University Hospital Tubeingen, Department for Anaesthesiology and Intensive Care Medicine | ||
Full Title: Serumspiegel von intravenös und enteral appliziertem Moxifloxacin bei kritisch kranken Intensivpatienten | ||
Medical condition: Patients, who are treated with Moxifloxacin due to clinical indication of respiratory infection or soft tissue infection | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2008-000550-12 | Sponsor Protocol Number: NRL920-01/2008 (IBSc) | Start Date*: 2008-11-06 | |||||||||||
Sponsor Name:Norgine Pharmaceuticals Ltd | |||||||||||||
Full Title: A Phase IIIb/IV, Multi-centre, Double-blind, Randomised, Placebo-controlled Parallel Group Study to Compare the Efficacy and Safety of Movicol® with Placebo in Patients with Constipation Associated... | |||||||||||||
Medical condition: Constipation associated with Irritable Bowel Syndrome (IBS-C). | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) DE (Completed) FR (Completed) IT (Completed) GB (Completed) CZ (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-005327-16 | Sponsor Protocol Number: | Start Date*: 2014-07-15 | |||||||||||
Sponsor Name:The University of Edinburgh [...] | |||||||||||||
Full Title: A Randomized Open Label Pilot Study to Compare Targinact vs. Oxycodone in Early Return of Gastrointestinal Function after Colorectal Surgery | |||||||||||||
Medical condition: Post-operative pain | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-000308-16 | Sponsor Protocol Number: prucalopride1 | Start Date*: 2011-10-24 | ||||||||||||||||
Sponsor Name:UZ Leuven | ||||||||||||||||||
Full Title: Prucalopride versus Placebo in Idiopathic and Diabetic Gastroparesis | ||||||||||||||||||
Medical condition: Patients with delayed gastric emptying (t1/2 for solids ≥ 109 min) either from idiopathic or diabetic origin | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: BE (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2020-004875-41 | Sponsor Protocol Number: Dropizol_healthy_2020 | Start Date*: 2021-01-02 | |||||||||||
Sponsor Name:Mech-Sense, Aalborg University Hospital | |||||||||||||
Full Title: Opium tincture against chronic diarrhea - Healthy: An investigator initiated, randomized placebo-controlled, double-blinded, cross-over, clinical trial | |||||||||||||
Medical condition: Chronic diarrhea - The effect of opium tincture on the gastrointestinal function | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-001275-21 | Sponsor Protocol Number: TAK-906-2002 | Start Date*: 2019-06-18 | |||||||||||||||||||||
Sponsor Name:Millennium Pharmaceuticals, Inc., a wholly owned subsidiary of Takeda Pharmaceutical Company Limited | |||||||||||||||||||||||
Full Title: A Multicenter, Randomized, Double-Blind, Placebo-Controlled, Parallel-Group, Phase 2b Study to Evaluate the Efficacy and Safety of Twice-Daily Oral Administration of a Peripherally Acting Dopamine ... | |||||||||||||||||||||||
Medical condition: Gastroparesis | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: BE (Completed) PL (Completed) IT (Prematurely Ended) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2010-023229-38 | Sponsor Protocol Number: TZP-101-CL-P008 | Start Date*: 2011-04-21 | |||||||||||
Sponsor Name:Tranzyme, Inc | |||||||||||||
Full Title: A Multicenter, Randomized, Double-Blind, Placebo-Controlled Study to Evaluate the Efficacy and Safety of Intravenous (IV) Ulimorelin Administered Post-Operatively to Accelerate Recovery of Gastroin... | |||||||||||||
Medical condition: post-operative ileus in subjects who have undergone partial bowel resection | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) LT (Completed) CZ (Completed) ES (Ongoing) BG (Completed) HU (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-002313-18 | Sponsor Protocol Number: PAMORA-AP_2020 | Start Date*: 2020-12-22 | |||||||||||
Sponsor Name:Mech-Sense, Aalborg University Hospital | |||||||||||||
Full Title: The effects of opioid receptor antagonism on acute pancreatitis: An investigator initiated, randomized, placebo-controlled, double-blind clinical trial | |||||||||||||
Medical condition: Acute pancreatitis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
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