- Trials with a EudraCT protocol (79)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (6)
79 result(s) found for: Dyspepsia.
Displaying page 1 of 4.
EudraCT Number: 2008-006405-17 | Sponsor Protocol Number: FDM-study | Start Date*: 2009-02-25 | |||||||||||
Sponsor Name:Kuopio University Hospital | |||||||||||||
Full Title: Finnish Dyspepsia Management -study | |||||||||||||
Medical condition: Tutkimukseen rekrytoidaan n. 400 dyspepsiaoireiden vuoksi erikoissairaanhoitoon lähetettyä alle 60-vuotiasta potilasta, joiden vaiva tutkimusten jälkeen todetaan toiminnalliseksi. | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2004-002612-28 | Sponsor Protocol Number: CHTF919D2301E1 | Start Date*: 2004-11-17 |
Sponsor Name:Novartis Pharmaceuticals UK Ltd | ||
Full Title: A one year, open label, multi-center, extension study to CHTF919D2301 to assess the long term safety of tegaserod 6 mg bid given orally in female patients with symptoms of dyspepsia | ||
Medical condition: dyspepsia | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2006-003194-27 | Sponsor Protocol Number: ML3602 | Start Date*: 2006-08-02 | |||||||||||
Sponsor Name:University Hospitals KU Leuven | |||||||||||||
Full Title: mirtazapine versus placebo in functional dyspepsia: a randomized, double-blind, placebo-controlled trial | |||||||||||||
Medical condition: functional dyspepsia diagnosed according to international consensus criteria ("Rome II criteria") | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-005747-42 | Sponsor Protocol Number: 1255/08 | Start Date*: 2009-02-03 | |||||||||||
Sponsor Name:POLICLINICO UNIVERSITARIO AGOSTINO GEMELLI | |||||||||||||
Full Title: Efficacy of a medical product containing sorbitol, simethicone and citrate potassium, in comparison with domperidone in patients affected by disfunctional dyspepsia: randomized monocentric cross-ov... | |||||||||||||
Medical condition: dysfunctional dyspepsia | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-001864-36 | Sponsor Protocol Number: Rikkunshito1 | Start Date*: 2015-10-09 | |||||||||||
Sponsor Name:uzleuven | |||||||||||||
Full Title: A PLACEBO-CONTROLLED STUDY ON THE EFFECT OF RIKKUNSHITO ON GASTRIC ACCOMMODATION AND NUTRIENT TOLERANCE, QUANTIFIED BY INTRAGASTRIC PRESSURE MONITORING DURING INTRAGASTRIC NUTRIENT INFUSION, IN FUN... | |||||||||||||
Medical condition: functional dyspepsia - postprandial distress syndrome | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-000059-17 | Sponsor Protocol Number: RVK28353 | Start Date*: 2011-02-22 | |||||||||||
Sponsor Name:Koege Hospital | |||||||||||||
Full Title: The clinical significance of acid rebound: Symptoms of reflux after 8 weeks of PPI treatment in patients with functional dyspepsia. | |||||||||||||
Medical condition: "Acid-Rebound Hypersecretion" and "Functional dyspepsia" | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-000436-24 | Sponsor Protocol Number: AGI006-001 | Start Date*: 2005-04-08 | |||||||||||
Sponsor Name:AGI Therapeutics Limtied | |||||||||||||
Full Title: A randomised, double-blind, placebo-controlled study of AGI 006 in the treatment of functional dyspepsia. | |||||||||||||
Medical condition: Functional (Non-ulcer) Dyspepsia (FD; NUD) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IE (Completed) LT (Completed) LV (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: 2005-001282-34 | Sponsor Protocol Number: ITOFD04-01 | Start Date*: 2005-07-30 |
Sponsor Name:AXCAN PHARMA Inc. | ||
Full Title: A multicentre, randomized, double-blind, placebo-controlled study of the efficacy and safety 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: GB (Completed) DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2016-003739-40 | Sponsor Protocol Number: 59153 | Start Date*: 2017-03-06 |
Sponsor Name:AMC Amsterdam | ||
Full Title: The effect of Iberogast on heartburn in patients with dyspepsia | ||
Medical condition: Dyspepsia (according to the Rome III criteria) with heartburn. Upper gastro-intestinal causes of the complaints excluded via gastroscopy | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: NL (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: 2005-005621-55 | Sponsor Protocol Number: 99010206E | Start Date*: 2006-06-14 | |||||||||||
Sponsor Name:Zeria Pharmaceutical Co., Ltd. | |||||||||||||
Full Title: Z-338:A Phase IIb, Multicentre, Randomised, Double-blind, Parallel-group, Placebo-controlled Study to Evaluate the Efficacy and Safety in Subjects with Functional Dyspepsia | |||||||||||||
Medical condition: Functional Dyspepsia | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Completed) DE (Completed) GB (Completed) BE (Completed) HU (Completed) ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-004296-39 | Sponsor Protocol Number: LPDSItopride | Start Date*: 2013-07-11 | |||||||||||
Sponsor Name:Targid University Leuven | |||||||||||||
Full Title: Functional Dyspepsia: validation of a questionnaire for symptom assessment in patients suffering from Postprandial Distress Syndrome (Functional Dyspepsia): assessment of sensitivity to change in P... | |||||||||||||
Medical condition: Functional dyspepsia, postprandial distress syndrome | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-000789-35 | Sponsor Protocol Number: HPTM06/J/05 | Start Date*: 2006-10-06 |
Sponsor Name:INFAI GmbH | ||
Full Title: Two-way Crossover Comparison of the Sensitivity and Specificity of the Modified Helicobacter Test INFAI Using New Test Meal vs. Standard 13C-Urea Breath Test in Helicobacter Pylori Positive and Neg... | ||
Medical condition: Diagnosis of Helicobacter pylori infection for patients taking proton pump inhibitors (PPI) without interuption of medication two weeks prior to test. | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: CZ (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2004-004748-27 | Sponsor Protocol Number: Acadmed CTU01/05 | Start Date*: 2005-02-21 | |||||||||||
Sponsor Name:Hull and east Yorkshire Hospitals Trust, Research and Deveopment, admin porta cabin | |||||||||||||
Full Title: An 8 week, double-blind, randomised, parallel group study to investigate the effect of 20 mg Esomeprazole (Nexium) tablets Twice daily versus placebo on symptoms associated with chronic cough due ... | |||||||||||||
Medical condition: We will be using Nexium to treat gastro-oesophageal reflux and in return this will reduce reflux related cough ( a manifestation of reflux) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-003342-16 | Sponsor Protocol Number: Z338-01 | Start Date*: 2014-02-24 | |||||||||||
Sponsor Name:Zeria Pharmaceutical Co., Ltd. | |||||||||||||
Full Title: A Phase III, Multicentre, Single-arm, Open-label Study to Evaluate the Long-term Safety of Z-338 in Subjects with Functional Dyspepsia | |||||||||||||
Medical condition: Functional Dyspepsia | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) SK (Completed) GB (Completed) LV (Completed) LT (Completed) BG (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-003631-37 | Sponsor Protocol Number: UDC1 | Start Date*: 2017-01-24 |
Sponsor Name:Universitaire ziekenhuis Leuven | ||
Full Title: Therapeutic effect of ursodeoxycholic acid on duodenal permeability and meal related sensory motor function 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: 2004-000448-26 | Sponsor Protocol Number: ITOFD04-03 | Start Date*: 2005-01-05 |
Sponsor Name:Axcan Pharma Inc. (Axcan Pharma International BV is subsidiary of Axcan Pharma Inc.) | ||
Full Title: A multicentre, randomized, double-blind, placebo-controlled study of the efficacy and safety 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: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2013-002705-65 | Sponsor Protocol Number: PrucaloprideGastro1 | Start Date*: 2013-09-26 |
Sponsor Name:TARGID | ||
Full Title: The effect of Prucalopride (Resolor) on gastric motor function and gastric sensitivity | ||
Medical condition: Functional dyspepsia | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: View results |
EudraCT Number: 2014-002092-28 | Sponsor Protocol Number: acotiamide1 | Start Date*: 2017-04-19 |
Sponsor Name:KULeuven - TARGID | ||
Full Title: The effect of acotiamide on gastric motility and satiation in healthy volunteers | ||
Medical condition: Funtional gastroenterological disorder: Functional Dyspepsia more specific the postprandial distress syndrome. | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: View results |
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