- Trials with a EudraCT protocol (46)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
46 result(s) found for: Functional Dyspepsia.
Displaying page 2 of 3.
EudraCT Number: 2017-003307-21 | Sponsor Protocol Number: 848016005-02 | Start Date*: 2018-05-30 |
Sponsor Name:Maastricht University | ||
Full Title: Tailored treatment of functional dyspepsia with nortriptyline: a multi-center double-blind placebo-controlled trial (TENDER) | ||
Medical condition: Functional dyspepsia (FD) | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: NL (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2008-008010-39 | Sponsor Protocol Number: HPTM11/J/08 | Start Date*: 2009-04-23 |
Sponsor Name:INFAI Institut für biomedizinische Analytik und NMR Imaging GmbH | ||
Full Title: The Sensivity and Specificity of the Modified Helicobacter Test INFAI Using New Test Meal with 13C-Urea Breath Test in Helicobacter Pylori Positive and Negative Patients with Dyspepsia Taking Proto... | ||
Medical condition: Diagnosis of Helicobacter pylori infection for patients taking proton pump inhibitors (PPI) with one day break of medication instead of two weeks prior to the test | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: DE (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2017-001369-25 | Sponsor Protocol Number: HPT30/J/17 | Start Date*: 2018-03-19 |
Sponsor Name:INFAI Institut für biomedizinische Analytik und NMR Imaging GmbH | ||
Full Title: The Sensitivity and Specificity of the Modified Helicobacter Test INFAI Using New Test Meal with 13C-Urea Breath Test in Helicobacter Pylori Positive and Negative Patients with Dyspepsia and GERD T... | ||
Medical condition: Diagnosis of Helicobacter pylori infection for patients taking proton pump inhibitors (PPI) with one day break of medication instead of two weeks prior to the test | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2007-005008-41 | Sponsor Protocol Number: 2007033 | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:Procter & Gamble Pharmaceuticals | |||||||||||||
Full Title: A Phase II, Randomized, Adaptive Design, Multicenter, Parallel Group, Placebo-controlled, 58-day, Dose-ranging Study of ATI-7505 in Patients with Postprandial Distress Syndrome | |||||||||||||
Medical condition: Postprandial Distress Syndrome | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) BE (Completed) IT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-002762-38 | Sponsor Protocol Number: Clin-AGI001-001 | Start Date*: 2005-04-13 | |||||||||||
Sponsor Name:AGI Therapeutics Limited | |||||||||||||
Full Title: A randomised, double-blind, placebo-controlled study of AGI 001 in the treatment of functional dyspepsia | |||||||||||||
Medical condition: Functional (Non-ulcer) Dyspepsia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: LT (Completed) GB (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2004-004308-19 | Sponsor Protocol Number: ITOFD04-04 | Start Date*: 2005-02-23 |
Sponsor Name:AXCAN PHARMA Inc. | ||
Full Title: A multicentre, open-label study to evaluate the long-term safety and efficacy of itopride HCl in patients suffering from functional dyspepsia | ||
Medical condition: Treatment of abdominal symptoms in patients with functional dyspepsia | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: DE (Prematurely Ended) BE (Completed) | ||
Trial results: View results |
EudraCT Number: 2014-004862-89 | Sponsor Protocol Number: mirtazapine1 | Start Date*: 2015-02-16 |
Sponsor Name:KULeuven | ||
Full Title: The effect of mirtazapine (REMERGON®) on gastric motility and satiation in healthy subjects | ||
Medical condition: Functional Dyspepsia | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: View results |
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: 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: 2014-005467-32 | Sponsor Protocol Number: n.a. | Start Date*: 2016-08-08 |
Sponsor Name:Haga Teaching Hospital | ||
Full Title: A randomised controlled trial on the effect of laxative therapy in children with functional abdominal pain | ||
Medical condition: Functional abdominal pain | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2009-010547-13 | Sponsor Protocol Number: Amisulpiride01 | Start Date*: 2010-09-16 | |||||||||||
Sponsor Name:UZLeuven | |||||||||||||
Full Title: Amisulpride versus Placebo in Functional Dyspespia with delayed gastric emptying | |||||||||||||
Medical condition: delayed gastric emptying | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) | |||||||||||||
Trial results: (No results available) |
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: 2013-001256-36 | Sponsor Protocol Number: FACH/023212 | Start Date*: 2013-06-14 | |||||||||||
Sponsor Name:Fachingen Heil- und Mineralbrunnen GmbH | |||||||||||||
Full Title: Pilot study with Staatl. Fachingen STILL for functional dyspepsia (particularly heartburn) | |||||||||||||
Medical condition: Functional dyspeptic complaints, particularly heartburn (at least 3 months prior to study start, at least twice per week) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-000994-19 | Sponsor Protocol Number: GER/026115 | Start Date*: 2016-07-08 | |||||||||||
Sponsor Name:Gerolsteiner Brunnen GmbH & Co. KG | |||||||||||||
Full Title: Doubleblind, randomised, placebo-controlled clinical trial to evaluate the safety and efficacy of Gerolsteiner Heilwasser in NERD patients with heartburn | |||||||||||||
Medical condition: functional dyspeptic complaints, particularly heartburn (at least 3 months prior to study start, on at least 4 days per week) | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-003293-32 | Sponsor Protocol Number: Duski2015 | Start Date*: 2017-11-06 | ||||||||||||||||
Sponsor Name:Academic Medical Center | ||||||||||||||||||
Full Title: Multicentre, Randomised, Placebo-Controlled Trial of Mebeverine in Children with Irritable Bowel Syndrome (IBS) or Functional Abdominal Pain - not otherwise specified (FAP-NOS) | ||||||||||||||||||
Medical condition: Functional Gastrointestinal Disorders (Irritable Bowel Syndrome or Functional Abdominal Pain - not otherwise specified) | ||||||||||||||||||
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Population Age: Adolescents, Under 18 | Gender: Male, Female | |||||||||||||||||
Trial protocol: NL (Ongoing) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-006258-99 | Sponsor Protocol Number: ECAMTEHP0012012 | Start Date*: 2012-04-02 | |||||||||||
Sponsor Name:Sección de Digestivo. Hospital Comarcal de Laredo | |||||||||||||
Full Title: FIRST-LINE ERADICATOR THERAPY OF HELICOBACTER PYLORI INFECTION: OPEN CLINICAL TRIAL, RANDOMIZED, MULTICENTRE, THREE-ARMED, COMPARING THE CLASSICAL TRIPLE THERAPY VERSUS A MODIFIED SEQUENTIAL THERAP... | |||||||||||||
Medical condition: Clinical situations where it is recommended the eradication of Helicobacter pylori: - Gastric or duodenal ulcer (active or not) and duodenal erosions - Gastric MALT lymphoma - First-degree relat... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-000533-31 | Sponsor Protocol Number: 17GA001 | Start Date*: 2017-11-07 | ||||||||||||||||
Sponsor Name:Nottingham University Hospitals NHS Trust | ||||||||||||||||||
Full Title: TReatment of Irritable bowel syndrome using Titrated ONdansetron Trial | ||||||||||||||||||
Medical condition: Irritable Bowel Syndrome with Diarrhoea | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-001584-22 | Sponsor Protocol Number: VDM/032711 | Start Date*: 2013-09-16 | |||||||||||
Sponsor Name:Gerolsteiner Brunnen GmbH & Co. KG | |||||||||||||
Full Title: Pilot study with St. Gero for heartburn | |||||||||||||
Medical condition: Functional dyspeptic complaints, particularly heartburn (at least 3 months prior to study start, at least twice per week) | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-002668-28 | Sponsor Protocol Number: HP-301 | Start Date*: 2020-04-21 | |||||||||||
Sponsor Name:Phathom Pharmaceuticals, Inc. | |||||||||||||
Full Title: A Phase 3 Randomized Multicenter Study to Evaluate the Efficacy and Safety of Open-Label Dual Therapy with Oral Vonoprazan 20 mg or Double-Blind Triple Therapy with Oral Vonoprazan 20 mg Compared t... | |||||||||||||
Medical condition: Helicobacter pylori infection | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) GB (GB - no longer in EU/EEA) CZ (Completed) PL (Completed) BG (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-002782-38 | Sponsor Protocol Number: Gastro052011 | Start Date*: 2012-07-06 |
Sponsor Name:INFAI GmbH | ||
Full Title: Gastromotal 13C-octanoic acid breath test in the diagnosis and evaluation of therapeutic outcome in patients with dyspeptic symptoms and delayed gastric emptying | ||
Medical condition: Patients with dyspeptic symptoms and delayed gastric emptying. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Ongoing) | ||
Trial results: (No results available) |
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