- Trials with a EudraCT protocol (86)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
86 result(s) found for: Proton therapy.
Displaying page 1 of 5.
EudraCT Number: 2016-003329-40 | Sponsor Protocol Number: 15-API-01 | Start Date*: 2017-09-19 | |||||||||||
Sponsor Name:CHU de Nice | |||||||||||||
Full Title: Neovascular glaucoma prevention by intravitreal injections of anti-VEGF in patients treated by protontherapy in case of large choroid melanoma | |||||||||||||
Medical condition: | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-003671-17 | Sponsor Protocol Number: NANOPRO | Start Date*: 2021-02-15 | |||||||||||
Sponsor Name:Centre François Baclesse | |||||||||||||
Full Title: Nanoparticle reirradiation and hypofractionated protontherapy of pan-tumor relapse: non-randomized phase II study. | |||||||||||||
Medical condition: recurrent tumors | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-002067-26 | Sponsor Protocol Number: PPH-KK01 | Start Date*: 2013-07-11 |
Sponsor Name:Landspitali University Hospital | ||
Full Title: Difference between dosages needed of proton pump inhibitors for females and males | ||
Medical condition: Erosive oesophagitis | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: IS (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2017-004248-39 | Sponsor Protocol Number: PPI-microbiome | Start Date*: 2018-01-04 |
Sponsor Name:TARGID, KU Leuven | ||
Full Title: Effect of Proton Pump Inhibitors on the duodenal microbiome in healthy volunteers | ||
Medical condition: We will assess the effect of Proton Pump Inhibitors (PPI) on the duodenal, oral and fecal microbiota composition in healthy volunteers | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: View results |
EudraCT Number: 2012-000603-32 | Sponsor Protocol Number: NL3364409612 | Start Date*: 2012-08-27 |
Sponsor Name:Annadalstichting | ||
Full Title: Proton pump inhibitors in the prevention of iron reaccumulation in patients with hereditary hemochromatosis | ||
Medical condition: Hereditary hemochromatosis | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2013-001080-23 | Sponsor Protocol Number: R+OCA | Start Date*: 2014-05-26 | |||||||||||
Sponsor Name:Javier P. Gisbert | |||||||||||||
Full Title: Rifaximin associated with the classic triple therapy (inhibitor proton pump, amoxicillin and clarithromycin) for eradication of Helicobacter pylori infection | |||||||||||||
Medical condition: Helicobacter pylori infection | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-004174-34 | Sponsor Protocol Number: Citalopram2017 | Start Date*: 2018-04-10 |
Sponsor Name:Targid, KU Leuven | ||
Full Title: A placebo-controlled trial with citalopram for the treatment of typical reflux symptoms in patients with reflux hypersensitivity or functional heartburn with incomplete proton pump inhibitor response | ||
Medical condition: Functional heartburn and reflux hypersensitivity with incomplete respons to proton pomp inhibitors | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: BE (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2022-003716-91 | Sponsor Protocol Number: CGB-1108 | Start Date*: 2023-02-21 | |||||||||||
Sponsor Name:Centrum Gastroenterologie Bethanien | |||||||||||||
Full Title: Randomized controlled clinical trial to evaluate the efficacy of alginates in washout of proton pump inhibitor therapy with consideration of compliance and symptom burden in patients with gastroeso... | |||||||||||||
Medical condition: Randomized controlled clinical trial to evaluate the efficacy of alginates in washout of proton pump inhibitor therapy with consideration of compliance and symptom burden in patients with gastroeso... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-004355-23 | Sponsor Protocol Number: PPI-microbiome-FD | Start Date*: 2018-01-04 |
Sponsor Name:TARGID, KU Leuven | ||
Full Title: Effect of Proton Pump Inhibitors on the duodenal microbiome 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: 2020-005340-39 | Sponsor Protocol Number: S64807 | Start Date*: 2021-02-01 |
Sponsor Name:University Hospitals Leuven | ||
Full Title: Duodenal neuro-immune interactions and effects of proton pump inhibitors in functional dyspepsia | ||
Medical condition: Functional Dyspepsia (FD) | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2006-000368-10 | Sponsor Protocol Number: NEX-426-MEI-0040-I | Start Date*: 2006-08-10 |
Sponsor Name:Tecnical University of Munich | ||
Full Title: High-dose therapy with Esomeprazol in combination with Baclofen therapy for symptomatic therapy-resistant gastrooesophageal reflux disease. | ||
Medical condition: Gastroesophageal reflux disease | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2011-004388-62 | Sponsor Protocol Number: SPD557-206 | Start Date*: 2012-04-24 | |||||||||||
Sponsor Name:Shire-Movetis NV | |||||||||||||
Full Title: A Phase 2b, Double-blind, Randomized, Placebo-controlled, Dose-finding Study to Evaluate Efficacy of a Selective 5-HT4 Receptor Agonist and Proton Pump Inhibitor (PPI) in subjects with Gastroesoph... | |||||||||||||
Medical condition: Gastroesophageal reflux disease (GERD) with persistent symptoms of regurgitation (with or without heartburn) while on a proton pump inhibitor therapy. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: PL (Completed) HU (Completed) DE (Completed) BE (Completed) LV (Completed) CZ (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-005203-32 | Sponsor Protocol Number: NERONE | Start Date*: 2012-04-17 | |||||||||||
Sponsor Name:UNIVERSITA' CAMPUS BIOMEDICO | |||||||||||||
Full Title: A prospective, multicenter, open-label, patients with non-erosive gastroesophageal reflux disease (NERD) non-responders to therapy with PPIs | |||||||||||||
Medical condition: non-erosive gastroesophageal reflux disease and apparently resistant to medical therapy with proton pump inhibitors | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-004175-31 | Sponsor Protocol Number: Prucalopride2017 | Start Date*: 2018-04-09 |
Sponsor Name:TARGID, KU Leuven | ||
Full Title: A placebo-controlled trial with prucalopride for the treatment of typical reflux symptoms in patients with gastro-esophageal reflux disease with incomplete proton pump inhibitor response | ||
Medical condition: refractory gastro-esophageal reflux disease | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: BE (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2014-000334-30 | Sponsor Protocol Number: INT27/14 | Start Date*: 2014-09-17 | |||||||||||
Sponsor Name:Fondazione IRCCS ''IStituto Nazionale dei Tumori'' | |||||||||||||
Full Title: Immunomodulatory effect of esomeprazole antitumoral and high-dose under neoadjuvant and adjuvant in patients with melanoma in stage III. Randomized pilot study treatment vs control | |||||||||||||
Medical condition: metastatic melanoma BLS+ and BRAF wt | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-004249-17 | Sponsor Protocol Number: NCTU:6831 | Start Date*: 2014-02-12 |
Sponsor Name:The Newcastle upon Tyne Hospitals NHS Foundation Trust | ||
Full Title: A randomised, placebo controlled trial of extra-oesophageal reflux treatment in the management of upper respiratory symptoms. [TOPPITS: Trial of Proton Pump Inhibitors in Throat Symptoms] | ||
Medical condition: Persistent throat symptom - globus, hoarseness, throat clearing, throat discomfort, choking spasms, excess mucus/postnasal drip, otherwise unexplained night time cough of choking. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2010-021397-12 | Sponsor Protocol Number: M0003-C202 | Start Date*: 2010-11-23 | |||||||||||
Sponsor Name:Shire-Movetis NV | |||||||||||||
Full Title: An explorative, randomized, placebo-controlled, double-blind, parallel-group trial, to evaluate the pharmacodynamic effect of M0003 on reflux parameters in subjects with gastroesophageal reflux dis... | |||||||||||||
Medical condition: Gastrointestinal esophageal reflux disease (GERD) refractory to proton pump inhibitor therapy | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) FR (Completed) DE (Prematurely Ended) GB (Completed) NL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-011543-40 | Sponsor Protocol Number: R324 | Start Date*: 2009-07-09 |
Sponsor Name:Papworth Hospital | ||
Full Title: Assessment of platelet inhibitory response to clopidogrel when coadministered with a proton pump inhibitor | ||
Medical condition: To investigate in patients undergoing elective coronary stenting, the interaction between omeprazole, rabeprazole and ranitidine on clopodogrel inhibition of platelet activity in wild type (wt/wt) ... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2006-002346-11 | Sponsor Protocol Number: IKP102/2006 | Start Date*: 2006-08-21 |
Sponsor Name:Medical Faculty, Otto-von-Guericke University | ||
Full Title: Stereoselective pharmacokinetics and CYP2C19-genotyping as outcome predictors of an omeprazole therapy in patients with GERD -- a pilot study (phase IV-study) | ||
Medical condition: The presented study has to evaluate whether an optimized individual dosage of proton pump inhibitors, adjusted to CYP2C19 genotype, leads to a better pharmakodynamic effect (pH metric acid suppress... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2019-001914-41 | Sponsor Protocol Number: KCT05-2019-BIZMUT-SI | Start Date*: 2020-03-09 |
Sponsor Name:Slovensko Združenje za gastroenterologijo in hepatologijo | ||
Full Title: Prospective randomised trial of first line treatments of Helicobacter pylori infection in Slovenia | ||
Medical condition: The purpose of the study is to determine the effectiveness of two first-line treatment regimens for Helicobacter pylori. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: SI (Completed) | ||
Trial results: (No results available) |
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