- Trials with a EudraCT protocol (13)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
13 result(s) found for: Barrett's esophagus.
Displaying page 1 of 1.
EudraCT Number: 2005-006191-35 | Sponsor Protocol Number: D9612L00088 | Start Date*: 2006-08-01 | |||||||||||
Sponsor Name:HSK, Dr. Horst Schmidt Kliniken GmbH | |||||||||||||
Full Title: Tumorfreies Überleben nach Ablation von Barrett-Schleimhaut Plus Esomeprazol versus tumorfreies Überleben unter Esomeprazol ohne Ablation von Barrett-Schleimhaut bei Patienten, die von einem „Barre... | |||||||||||||
Medical condition: Endoscopically treated Barrett-adenocarcinoma with complete remission | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-001034-14 | Sponsor Protocol Number: 07/Q0803/31 | Start Date*: 2007-08-10 | ||||||||||||||||
Sponsor Name:St George's Healthcare NHS Trust [...] | ||||||||||||||||||
Full Title: The effect of omega-3 fatty acids on Barrett's oesophagus | ||||||||||||||||||
Medical condition: Barrett's oesophagus refers to changes in the lining of the lower oesophagus in response to injury caused by gastric reflux. It is a pre-malignant condition and has a well established link with ad... | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (Prematurely Ended) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2008-002446-39 | Sponsor Protocol Number: CUV025 | Start Date*: 2008-10-16 | ||||||||||||||||
Sponsor Name:Clinuvel Pharmaceuticals Limited | ||||||||||||||||||
Full Title: A Phase II, Multicentre, Double-blind, Placebo Controlled, Pilot Study to Evaluate the Safety and Efficacy of CUV1647 Administered as A Subcutaneous Bioresorbable 16mg Implant in Patients Undergoin... | ||||||||||||||||||
Medical condition: Barrett's Oesohagus Cholangiocarcinoma | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: FR (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: 2011-000264-10 | Sponsor Protocol Number: ICS10/0273 | Start Date*: 2011-09-14 | |||||||||||
Sponsor Name:Instituto Aragonés de Ciencias de la Salud | |||||||||||||
Full Title: Melatonina asociada a inhibición ácida como estrategia de quimioprevención en esófago de Barrett. Estudio piloto | |||||||||||||
Medical condition: Progresión de esófago de Barrett a adenocarcinoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-002418-22 | Sponsor Protocol Number: T-016 | Start Date*: 2014-11-07 | ||||||||||||||||||||||||||
Sponsor Name:Trio Medicines Ltd | ||||||||||||||||||||||||||||
Full Title: Randomized, placebo-controlled trial of YF476, a gastrin receptor antagonist, in Barrett’s esophagus (10-505; T-016) | ||||||||||||||||||||||||||||
Medical condition: Barrett's oesophagus | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: GB (Completed) | ||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2018-002617-35 | Sponsor Protocol Number: BUL-5/ESD | Start Date*: 2019-08-20 | |||||||||||||||||||||
Sponsor Name:Dr. Falk Pharma GmbH | |||||||||||||||||||||||
Full Title: Double-blind, randomised, placebo-controlled, phase IIa trial on the efficacy and tolerability of an 8-week treatment with two different doses of budesonide orodispersible tablets vs. placebo for p... | |||||||||||||||||||||||
Medical condition: Prevention of oesophageal strictures in adult patients after endoscopic submucosal dissection | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: DE (Restarted) PT (Trial now transitioned) NL (Trial now transitioned) BE (Completed) SE (Trial now transitioned) PL (Trial now transitioned) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-001183-37 | Sponsor Protocol Number: n.a. | Start Date*: 2008-06-02 |
Sponsor Name:Erasmus MC | ||
Full Title: PROSPECTIVE RANDOMIZED COMPARISON OF EMR VERSUS EMR FOLLOWED BY PHOTODYNAMIC THERAPY FOR THE TREATMENT OF EARLY BARRETT’S CANCER | ||
Medical condition: high grade dysplasia and early carcinoma in Barrett Esophagus | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
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: 2018-004745-17 | Sponsor Protocol Number: UMCG:201800879 | Start Date*: 2019-03-28 |
Sponsor Name:University Medical Center Groningen | ||
Full Title: Detection of Early Esophageal Cancer by Near-Infrared Fluorescence molecular Endoscopy using Bevacizumab-800CW | ||
Medical condition: Patients with Barretts esophagus and there is a suspicion for at least low grade dysplasia. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2008-002721-37 | Sponsor Protocol Number: CLBH589BDE03T | Start Date*: 2009-06-09 |
Sponsor Name:Medizinische Fakultät der TU-München, vertreten durch den Dekan | ||
Full Title: An open-label, uncontrolled phase II trial of HDAC inhibitor LBH589 in patients with chemo-refractory metastatic gastric cancer overexpressing histone deacetylases - CLBH589BDE03T | ||
Medical condition: A study with patients with chemo-refractory metastatic gastric cancer overexpressing histone deacetylases (HDACs) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2006-000476-33 | Sponsor Protocol Number: GC-SU-2006 | Start Date*: 2006-11-20 | |||||||||||
Sponsor Name:Johannes-Gutenberg-Universität Mainz, I. Medizinische Klinik und Poliklinik | |||||||||||||
Full Title: An open-label, multicenter phase II trial of Sunitinib for patients with chemo-refractory metastatic gastric cancer | |||||||||||||
Medical condition: Chemorefractory metastatic adenocarcinoma of stomach, esophagogastric junction and lower esophagus (Barrett carcinoma) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (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 |
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