- Trials with a EudraCT protocol (8)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
8 result(s) found for: Atonia.
Displaying page 1 of 1.
| EudraCT Number: 2007-004997-23 | Sponsor Protocol Number: M0003-C201 | Start Date*: 2007-11-23 | |||||||||||
| Sponsor Name:Movetis NV | |||||||||||||
| Full Title: An exploratory, double-blind, randomized, stratified, placebo-controlled, repeated dose trial to investigate the efficacy of M0003 on symptoms suggestive for gastroparesis, to assess the pharmacody... | |||||||||||||
| Medical condition: Symptoms suggestive for gastroparesis | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: BE (Completed) DE (Completed) LT (Completed) NL (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2015-005489-46 | Sponsor Protocol Number: OPEGG | Start Date*: 2016-02-02 | |||||||||||||||||||||
| Sponsor Name:Umeå University | |||||||||||||||||||||||
| Full Title: Recovery of gastric function after treatment with shortacting opioids. | |||||||||||||||||||||||
| Medical condition: The effect of opioids on gastric electrical activity | |||||||||||||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||||||||||||
| Trial protocol: SE (Prematurely Ended) | |||||||||||||||||||||||
| Trial results: View results | |||||||||||||||||||||||
| EudraCT Number: 2011-002594-33 | Sponsor Protocol Number: TZP-102-CL-G003 | Start Date*: 2011-10-14 | |||||||||||
| Sponsor Name:Tranzyme, Inc. | |||||||||||||
| Full Title: A Multicenter, Randomized, Double-Blind, Placebo-Controlled, Parallel-Group Evaluation of the Efficacy and Safety of Once-Daily Administrations of TZP 102 for the Treatment of Symptoms Associated w... | |||||||||||||
| Medical condition: The medical condition to be investigated is symptomatic gastroparesis due to diabetes mellitus | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: SE (Completed) FI (Completed) DK (Completed) DE (Completed) BE (Completed) PL (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2012-002576-14 | Sponsor Protocol Number: TZP-102-CL-G004 | Start Date*: 2012-08-23 | |||||||||||
| Sponsor Name:Tranzyme, Inc. | |||||||||||||
| Full Title: A Multicenter, Randomized, Double-Blind, Placebo-Controlled, Parallel-Group Evaluation of the Efficacy and Safety of TZP-102 Given Orally Three Times a Day for the Treatment of Symptoms Associate... | |||||||||||||
| Medical condition: The medical condition to be investigated is symptomatic gastroparesis due to diabetes mellitus | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: PL (Prematurely Ended) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2008-007226-19 | Sponsor Protocol Number: TZP-102-CL-G002 | Start Date*: 2009-05-15 | |||||||||||
| Sponsor Name:Tranzyme Inc. | |||||||||||||
| Full Title: A Multicenter, Randomized, Double-Blind, Placebo-Controlled, Parallel-Group, Phase 2 Evaluation of the Safety and Efficacy of Once-Daily Administrations of TZP 102 for the Treatment of Symptomatic... | |||||||||||||
| Medical condition: The medical condition to be investigated is gastroparesis due to diabetes mellitus. | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: SE (Completed) DK (Completed) GB (Completed) PL (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| 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: 2010-019563-11 | Sponsor Protocol Number: RB10001 | Start Date*: 2010-06-01 | ||||||||||||||||||||||||||
| Sponsor Name:RECKITT BENCKISER HEALTHCARE | ||||||||||||||||||||||||||||
| Full Title: Etude de non-infériorité de l’efficacité de Gaviscon suspension buvable en flacon versus Oméprazole 20mg sur le pyrosis chez des patients ayant un RGO dont l’épisode actuel n’est pas traité. | ||||||||||||||||||||||||||||
| Medical condition: Patient volontaire présentant un épisode de RGO non traité et venant consulter en médecine générale. | ||||||||||||||||||||||||||||
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| Population Age: Adults | Gender: Male, Female | |||||||||||||||||||||||||||
| Trial protocol: FR (Completed) | ||||||||||||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||||||||||||
| EudraCT Number: 2008-005135-15 | Sponsor Protocol Number: 8101 colloidAug08 | Start Date*: 2009-01-12 | ||||||||||||||||||||||||||||||||||||||||||||||
| Sponsor Name:University of Nottingham | ||||||||||||||||||||||||||||||||||||||||||||||||
| Full Title: Do 100 kiloDaltons matter? A prospective randomised double-blind study on the blood volume expanding effects of two different colloids in patients undergoing laparoscopic cholecystectomy | ||||||||||||||||||||||||||||||||||||||||||||||||
| Medical condition: Patients undergoing laparoscopic cholecystectomy | ||||||||||||||||||||||||||||||||||||||||||||||||
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| Population Age: Adults | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||||||||||||
| Trial protocol: GB (Completed) | ||||||||||||||||||||||||||||||||||||||||||||||||
| Trial results: View results | ||||||||||||||||||||||||||||||||||||||||||||||||
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