- Trials with a EudraCT protocol (45)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (8)
45 result(s) found for: Reflux esophagitis.
Displaying page 1 of 3.
EudraCT Number: 2004-000492-33 | Sponsor Protocol Number: BY1023/M3-904 | Start Date*: 2004-09-06 | |||||||||||
Sponsor Name:ALTANA Pharma AG | |||||||||||||
Full Title: Healing of patients suffering from gastroesophageal reflux esophagitis grade C-D according to Los Angeles classification after treatment with pantoprazole-magnesium dihydrate 80 mg o.d. in comparis... | |||||||||||||
Medical condition: Gastroesophageal reflux esophagitis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: LV (Completed) HU (Completed) LT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-000493-32 | Sponsor Protocol Number: BY1023/M3-906 | Start Date*: 2004-08-17 | |||||||||||
Sponsor Name:ALTANA Pharma AG | |||||||||||||
Full Title: Healing of patients suffering from gastroesophageal reflux esophagitis grade A-D according to Los Angeles classification after treatment with pantoprazole-magnesium dihydrate 80 mg o.d. in comparis... | |||||||||||||
Medical condition: Gastroesophageal reflux esophagitis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SK (Completed) CZ (Completed) AT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-004806-25 | Sponsor Protocol Number: BY1023/M3-339 | Start Date*: 2005-04-25 | |||||||||||
Sponsor Name:ALTANA Pharma AG | |||||||||||||
Full Title: Evaluation of the complete remission rates in patients with symptomatic non-erosive reflux disease (NERD) or erosive gastroesophageal reflux disease (GERD) treated with pantoprazole 40 mg o.d. ove... | |||||||||||||
Medical condition: Gastroesophageal reflux disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) AT (Completed) HU (Completed) | |||||||||||||
Trial results: View results |
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: 2008-001526-13 | Sponsor Protocol Number: 23/2008/O/Sper | Start Date*: 2008-06-03 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA DI BOLOGNA POLICLINICO S. ORSOLA M. MALPIGHI | |||||||||||||
Full Title: Efficacy of Gaviscon in the treatment of gastroesophageal reflux in preterm newborns | |||||||||||||
Medical condition: gastroesophageal reflux in preterm newborns | |||||||||||||
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Population Age: Preterm newborn infants, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-002934-12 | Sponsor Protocol Number: 77/2007/U/Sper | Start Date*: 2007-06-12 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA DI BOLOGNA POLICLINICO S. ORSOLA M. MALPIGHI | |||||||||||||
Full Title: MANTEINANCE TREATMENT IN NERD PATIENT. A COMPARATIVE RANDOMIZED OPEN STUDY BETWEEN ALGINATE AND MAGALDRATE. | |||||||||||||
Medical condition: Gastroesophageal reflux | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-000711-10 | Sponsor Protocol Number: BY1023/UK506 | Start Date*: 2005-07-07 | |||||||||||
Sponsor Name:ALTANA Pharma Ltd. | |||||||||||||
Full Title: Determination of the performance characteristics of ReQuestTM in Practice in the stepped down management of GORD | |||||||||||||
Medical condition: Gastro-oesophageal reflux disease | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-001302-16 | Sponsor Protocol Number: IKP103/2008 | Start Date*: 2008-06-30 | |||||||||||
Sponsor Name:Medical Faculty, Otto-von-Guericke University | |||||||||||||
Full Title: Stereoselective pharmacokinetics and CYP2C19-genotyping as outcome predictors of an esomeprazole 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 pharmacokinetic effect (pH metric acid suppress... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-017229-20 | Sponsor Protocol Number: KCT 27/2009 – PAN-STAR/PL | Start Date*: 2010-06-24 | |||||||||||
Sponsor Name:KRKA-POLSKA Sp. z o.o. | |||||||||||||
Full Title: Efficacy and safety of PANtoprazole in the treatment and SympTom relief in patients with gAstRoesophageal reflux disease (GERD) – PAN-STAR | |||||||||||||
Medical condition: gastroesophageal reflux disease (GERD) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: PL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-004232-29 | Sponsor Protocol Number: UZBLANREOTIDE01 | Start Date*: 2014-01-02 | |||||||||||
Sponsor Name:UZ Brussel | |||||||||||||
Full Title: A phase II proof of concept study to evalute the efficacy and safety of deep subcutaneous lanreotide Autogel 120 mg / 28 days on symptoms and healing of the esophageal and gastric mucosa in patient... | |||||||||||||
Medical condition: patients with persistent endoscopic reflux in spite of maximal medical therapy with PPI 2 x 40 mg pantoprazole before breakfast and dinner and 300 mg of H2 blocker ranitidine at bedtime AND continu... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-000926-30 | Sponsor Protocol Number: BY1023/M3-343 | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:ALTANA Pharma AG | |||||||||||||
Full Title: Investigation of clinical endpoints for treatment-induced gastroesophageal reflux disease (GERD) symptom changes | |||||||||||||
Medical condition: gastroesophageal reflux disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) AT (Completed) HU (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-001681-15 | Sponsor Protocol Number: TAK-390MR_207 | Start Date*: 2012-10-17 | |||||||||||||||||||||
Sponsor Name:Takeda Global Research & Development Centre (Europe) Ltd | |||||||||||||||||||||||
Full Title: A Phase 2 Multicenter, 36-Week Study to Assess the Safety and Effectiveness of Daily Oral Administration of Dexlansoprazole Delayed-Release Capsules for Healing of Erosive Esophagitis and Maintenan... | |||||||||||||||||||||||
Medical condition: Heartburn and Erosive Esophagitis in Adolescent Subjects | |||||||||||||||||||||||
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Population Age: Adolescents, Under 18 | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: HU (Completed) BE (Completed) PT (Completed) IT (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2007-002031-92 | Sponsor Protocol Number: EX0307 | Start Date*: Information not available in EudraCT | ||||||||||||||||||||||||||
Sponsor Name:Otto-von-Guericke University | ||||||||||||||||||||||||||||
Full Title: Proliferation and differentiation markers, involved in erosive and non-erosive reflux esophagitis, Barrett´s esophagus and esophageal adenocarcinoma. | ||||||||||||||||||||||||||||
Medical condition: Dyspeptic Symptoms GERD (gastroesophageal reflux disease), NERD (non erosive reflux disease), ERD (erosive reflux disease), Barretts esophagus, Adeno-CA of the esophagus | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: DE (Completed) | ||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2010-019563-11 | Sponsor Protocol Number: RB10001 | Start Date*: 2010-06-01 | ||||||||||||||||||||||||||
Sponsor Name:RECKITT BENCKISER HEALTHCARE | ||||||||||||||||||||||||||||
Full Title: Etude de non-infériorité de l’efficacité de Gaviscon suspension buvable en flacon versus Oméprazole 20mg sur le pyrosis chez des patients ayant un RGO dont l’épisode actuel n’est pas traité. | ||||||||||||||||||||||||||||
Medical condition: Patient volontaire présentant un épisode de RGO non traité et venant consulter en médecine générale. | ||||||||||||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: FR (Completed) | ||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2004-002370-39 | Sponsor Protocol Number: D9614C00097 | Start Date*: 2004-12-02 | |||||||||||
Sponsor Name:ASTRAZENECA | |||||||||||||
Full Title: A Phase III, Multicentre, Randomized, Double-blind Parallel-group Study to Evaluate the Safety and Clinical Outcome of Once Daily Esomeprazole for the Treatment of Gastroesophageal Reflux Disease ... | |||||||||||||
Medical condition: Gastroesophageal Reflux Disease GERD | |||||||||||||
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Population Age: Infants and toddlers, Children, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) Outside EU/EEA | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-003485-42 | Sponsor Protocol Number: BY1023/M3-341 | Start Date*: 2006-03-24 | |||||||||||
Sponsor Name:ALTANA Pharma AG | |||||||||||||
Full Title: Treatment response in patients with symptoms due to gastroesophageal reflux disease either with or without esophagitis treated with pantoprazole sodium 40 mg o.d. over 8 weeks | |||||||||||||
Medical condition: gastroesophageal reflux disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Completed) DE (Completed) ES (Completed) GB (Completed) IT (Completed) BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-000927-33 | Sponsor Protocol Number: BY1023/M3-342 | Start Date*: 2006-05-03 | |||||||||||
Sponsor Name:Nycomed GmbH | |||||||||||||
Full Title: Confirmation of superiority of complete remission concept vs classical healing concept for treatment of patients with erosive GERD | |||||||||||||
Medical condition: gastroesophageal reflux disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-004506-15 | Sponsor Protocol Number: TAK-390MR_204 | Start Date*: 2015-12-10 | |||||||||||
Sponsor Name:Takeda Development Centre Europe Ltd. | |||||||||||||
Full Title: A Phase 2, Double-Blind, 12 Week, Multicenter Study to Assess the Safety and Effectiveness of Daily Oral Administration of Dexlansoprazole Delayed-Release Capsules in Pediatric Subjects Aged 1 to ... | |||||||||||||
Medical condition: Symptomatic nonerosive GERD in paediatric subjects aged 1 to 11 years | |||||||||||||
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Population Age: Infants and toddlers, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) IT (Prematurely Ended) PT (Completed) PL (Trial now transitioned) LT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-002777-42 | Sponsor Protocol Number: BY359/M3-301 | Start Date*: 2006-11-07 | |||||||||||
Sponsor Name:ALTANA Pharma AG | |||||||||||||
Full Title: Endoscopic healing and tolerability of Soraprazan 20 mg qd compared to Soraprazan 10 mg qd and to Esomeprazole 40 mg qd in patients suffering from GERD Grade A-D (LA classification) | |||||||||||||
Medical condition: Endoscopically confirmed gastroesophageal reflux disease (GERD), Grade A-D according to Los Angeles (LA) classification | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: LT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
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 |
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