- Trials with a EudraCT protocol (22)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (10)
22 result(s) found for: Lansoprazole.
Displaying page 1 of 2.
EudraCT Number: 2019-002579-33 | Sponsor Protocol Number: EE-301 | Start Date*: 2020-03-26 | |||||||||||
Sponsor Name:Phathom Pharmaceuticals, Inc. | |||||||||||||
Full Title: A Phase 3, Randomized, Double-Blind, Two-Phase, Multicenter Study to Evaluate the Efficacy and Safety of Vonoprazan 20 mg Compared to Lansoprazole 30 mg for Healing in Patients with Erosive Esophag... | |||||||||||||
Medical condition: Erosive Esophagitis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) CZ (Completed) HU (Completed) PL (Completed) BG (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-003319-91 | Sponsor Protocol Number: CX842A2201 | Start Date*: 2021-02-08 | |||||||||||
Sponsor Name:Cinclus Pharma AG | |||||||||||||
Full Title: A randomized double-blind, double dummy, active comparator-controlled dose finding study in patients with reflux esophagitis Los Angeles grade C or D, and patients with at least partial symptom res... | |||||||||||||
Medical condition: reflux esophagitis Los Angeles grade C or D and patients with grades A or B who partially responded to PPI patients with grades A or B who partially responded to PPI | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) CZ (Completed) BG (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-001187-31 | Sponsor Protocol Number: T-EE04-084 | Start Date*: 2006-03-06 |
Sponsor Name:TAP Pharmaceutical Products Inc. | ||
Full Title: A Phase 3 Study to Evaluate the Efficacy and Safety of TAK-390MR (60 mg QD and 90 mg QD) and an Active Comparator, Lansoprazole (30 mgQD) on Healing of Erosive Esophagitis | ||
Medical condition: Erosive esophagitis | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: EE (Completed) LV (Completed) LT (Completed) CZ (Completed) DE (Completed) GB (Prematurely Ended) HU (Completed) SK (Completed) | ||
Trial results: View results |
EudraCT Number: 2005-001188-70 | Sponsor Protocol Number: T-EE04-085 | Start Date*: 2006-03-06 |
Sponsor Name:TAP Pharmaceutical Products Inc. | ||
Full Title: A Phase 3 Study to Evaluate the Efficacy and Safety of TAK-390MR (60 mg QD and 90 mg QD) and an Active Comparator, Lansoprazole (30 mgQD) on Healing of Erosive Esophagitis | ||
Medical condition: Erosive esophagitis | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: EE (Completed) LV (Completed) LT (Completed) CZ (Completed) HU (Completed) SK (Completed) | ||
Trial results: View results |
EudraCT Number: 2016-004021-16 | Sponsor Protocol Number: FIM-PXE-2016-01 | Start Date*: 2018-10-31 | |||||||||||
Sponsor Name:Fundación Pública Andaluza para la Investigación de Málaga en Biomedicina y Salud (FIMABIS) | |||||||||||||
Full Title: Response to oral lansoprazole in inorganic pyrophosphate levels in patients with Grönblad-Stranberg disease (Pseudoxanthoma Elasticum) | |||||||||||||
Medical condition: Grönblad-Stranberg disease (Pseudoxanthoma Elasticum) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
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: 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: 2020-000041-14 | Sponsor Protocol Number: 269050-80-06-19 | Start Date*: 2020-06-19 | |||||||||||
Sponsor Name:Norfolk and Norwich University Hospitals NHS Foundation Trust | |||||||||||||
Full Title: The effectiveness and risks of Treating people with Idiopathic Pulmonary fibrosis with the Addition of Lansoprazole (TIPAL): a randomised placebo-controlled multi-centre clinical trial | |||||||||||||
Medical condition: Idiopathic Pulmonary Fibrosis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
Trial results: (No results available) |
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: 2004-001633-42 | Sponsor Protocol Number: hp001 | Start Date*: 2005-01-06 |
Sponsor Name:NHS GRAMPIAN | ||
Full Title: Is there a role for Helicobacter pylori eradication in the treatment of laryngopharyngeal reflux? : A double blinded randomised case controlled clinical trial | ||
Medical condition: LARYNGOPHARYNGEAL ACID REFLUX | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2011-003425-96 | Sponsor Protocol Number: 11091 | Start Date*: 2011-12-15 |
Sponsor Name:University of Nottingham | ||
Full Title: Helicobacter eradication to prevent ulcer bleeding in aspirin users: a large simple randomised controlled trial | ||
Medical condition: Helicobacter eradication to prevent ulcer bleeding in aspirin users | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (GB - no longer in EU/EEA) | ||
Trial results: (No results available) |
EudraCT Number: 2016-001569-97 | Sponsor Protocol Number: AGO/2016/004 | Start Date*: 2017-06-19 |
Sponsor Name:University Hospital Ghent | ||
Full Title: A phase II Investigation of Pembrolizumab (Keytruda) in combination with radiation and an immune modulatory cocktail in patients with cervical and uterine cancer. | ||
Medical condition: cervical cancer, endometrial carcinoma, uterine sarcoma | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: BE (Completed) | ||
Trial results: View results |
EudraCT Number: 2020-004723-17 | Sponsor Protocol Number: UZBSK001 | Start Date*: 2021-02-26 |
Sponsor Name:UZ Brussel | ||
Full Title: Clinical usefulness and influence on oesophageal motility of pyridostigmine for dysphagia in systemic sclerosis. | ||
Medical condition: Dysphagia by patients suffering from systemic sclerosis | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: View results |
EudraCT Number: 2010-019154-40 | Sponsor Protocol Number: DOSAPI | Start Date*: 2010-05-19 | |||||||||||
Sponsor Name:Medco Health Solutions, Inc. | |||||||||||||
Full Title: Doubler la dose du clopidogrel ou passer au Prasugrel pour contrer l’interaction liée aux inhibiteurs de pompe à protons | |||||||||||||
Medical condition: Maladie des artères coronaires | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-004632-69 | Sponsor Protocol Number: P060309 | Start Date*: 2006-12-04 | |||||||||||
Sponsor Name:ASSISTANCE PUBLIQUE - HOPITAUX DE PARIS (AP-HP) | |||||||||||||
Full Title: Polymorphismes du gène codant pour le cytochrome 2C19 et réponse au clopidogrel chez le sujet sain | |||||||||||||
Medical condition: volontaire sain | |||||||||||||
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Population Age: Adults | Gender: Male | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-014539-20 | Sponsor Protocol Number: IGA-10612-3 | Start Date*: 2009-08-24 |
Sponsor Name:University Hospital Ostrava | ||
Full Title: The Position of Outpatient 24-Hour Dual-Probe pH-metry in the Diagnostics of Extraosophageal Reflux | ||
Medical condition: Ve studii budeme zkoumat extraezofageální reflux, jedná se o podskupinu refluxní nemoci jícnu, kdy jsou v popředí mimojícnové projevy kyselého refluxu. Závěry studií uzavírají, že EER v různé míře ... | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: CZ (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2013-000759-41 | Sponsor Protocol Number: 34 | Start Date*: 2014-03-27 |
Sponsor Name:Fondazione Toscana Gabriele Monasterio | ||
Full Title: A prospective, open-label, single center, cross-over, controlled, randomized, phase III study to test superiority of the oral solution of synthetic thyroxine compared to tablet preparation for tr... | ||
Medical condition: Hypothyroidism | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: IT (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2010-022260-12 | Sponsor Protocol Number: 1947 | Start Date*: 2011-03-24 | |||||||||||
Sponsor Name:King's College Hospital NHS Foundation Trust | |||||||||||||
Full Title: A Phase II trial of broad spectrum antibiotic therapy for early stage chronic lymphocytic leukaemia. | |||||||||||||
Medical condition: Chronic Lymphocytic Leukaemia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-003174-17 | Sponsor Protocol Number: GA1405 | Start Date*: 2015-03-24 |
Sponsor Name:Reckitt Benckiser Healthcare (UK) Limited | ||
Full Title: A multicentre, randomised, double-blind, two arm, parallel group, placebo controlled pivotal study to assess the effect of a sodium alginate liquid suspension as add-on therapy in GORD patients wit... | ||
Medical condition: Gastro-Oesophageal Reflux Disease (GORD) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2012-004470-25 | Sponsor Protocol Number: GA1214 | Start Date*: 2013-01-08 |
Sponsor Name:Reckitt Benckiser Healthcare (UK) Ltd | ||
Full Title: A multicentre, randomised, double-blind, two arm, parallel group, pilot study to assess the effect of Gaviscon® Double Action Mint as add-on therapy in GORD patients with inadequate response to onc... | ||
Medical condition: Patients with Gastro Oesophageal Reflux Disease (GORD) with inadequate response to PPI treatment | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
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