- Trials with a EudraCT protocol (7)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
7 result(s) found for: Hiatal Hernia.
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EudraCT Number: 2009-013080-19 | Sponsor Protocol Number: 27538 | Start Date*: 2010-03-31 | |||||||||||||||||||||||||||||||
Sponsor Name:AMC | |||||||||||||||||||||||||||||||||
Full Title: Prokinetics to alter the position of the gastric acid pocket in Gastro Esophageal Reflux Disease | |||||||||||||||||||||||||||||||||
Medical condition: gastro-esophageal reflux disease (GERD) | |||||||||||||||||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||||||||||||||||||||||
Trial protocol: NL (Ongoing) | |||||||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-003418-16 | Sponsor Protocol Number: Bac04018 | Start Date*: 2007-02-14 |
Sponsor Name:Academic Medical Center | ||
Full Title: The role of a hiatal hernia on the efficacy of anti-TLESR therapy in patients with gastroesophageal reflux disease | ||
Medical condition: Gastroesophageal reflux disease | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2012-002748-25 | Sponsor Protocol Number: ICP-112-201 | Start Date*: 2012-10-25 | |||||||||||
Sponsor Name:Ironwood Pharmaceuticals, Inc. | |||||||||||||
Full Title: A Multicenter, Randomized, Double-blind, Placebo-controlled, Parallel-group, Phase 2a Study of Oral IW-9179 Administered Once Daily for 14 Days to Patients with Functional Dyspepsia | |||||||||||||
Medical condition: Functional Dyspepsia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-000753-31 | Sponsor Protocol Number: RC19_0055 | Start Date*: 2019-07-04 | |||||||||||
Sponsor Name:CHU Nantes | |||||||||||||
Full Title: Evaluation of REMIFENTANIL as an alternative to curare for rapid sequence anesthetic induction in patients at risk of gastric fluid inhalation | |||||||||||||
Medical condition: anesthetic induction | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-002182-35 | Sponsor Protocol Number: buspirone2019 | Start Date*: 2019-09-10 |
Sponsor Name:KU Leuven - TARGID | ||
Full Title: The effect of oral buspirone hydrochloride on esophageal motility, bolus transit and symptoms of dysphagia, in patients with poor esophageal motility: A randomized, double-blind, placebo controlle... | ||
Medical condition: Patients with complaints of dysphagia and poor esophageal motility | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2016-004446-29 | Sponsor Protocol Number: LIBERAL-Trial | Start Date*: 2017-10-30 | |||||||||||
Sponsor Name:University Hospital Wuerzburg, Institution under public law, represented by the Medical Director | |||||||||||||
Full Title: Liberal transfusion strategy to prevent mortality and anaemia-associated, ischaemic events in elderly non-cardiac surgical patients | |||||||||||||
Medical condition: Elderly patients (>= 70 years) undergoing intermediate- or high-risk non-cardiac surgery | |||||||||||||
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Population Age: Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-001642-16 | Sponsor Protocol Number: TAK-390MR_108 | Start Date*: 2015-04-24 | ||||||||||||||||||||||||||
Sponsor Name:Takeda Development Centre Europe Ltd. | ||||||||||||||||||||||||||||
Full Title: A Phase 1, Randomized, Open-Label, Parallel-Design, Multicenter Study to Evaluate the Pharmacokinetics, Safety, and Pharmacodynamics of Dexlansoprazole Delayed-Release Capsules in Infants Aged 1 ... | ||||||||||||||||||||||||||||
Medical condition: Acid-Related Disorders in Infants aged 1 to 11 months | ||||||||||||||||||||||||||||
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Population Age: Infants and toddlers, Under 18 | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: IT (Temporarily Halted) PL (Completed) | ||||||||||||||||||||||||||||
Trial results: View results |
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