- Trials with a EudraCT protocol (336)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (1)
336 result(s) found for: Esophageal disease.
Displaying page 1 of 17.
EudraCT Number: 2009-013259-31 | Sponsor Protocol Number: 6232 | Start Date*: 2009-12-29 | ||||||||||||||||
Sponsor Name:UMC Utrecht | ||||||||||||||||||
Full Title: A multicenter double blind placebo-controlled randomised trial for benign esophageal anastomotic strictures: Savary dilation vs savary dilation with Triamcinolon | ||||||||||||||||||
Medical condition: Patients with first time dysphagia (grade 2-4) due to a benign anastomotic esophageal stricture | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: NL (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-018298-39 | Sponsor Protocol Number: botox2010 | Start Date*: 2010-02-15 | |||||||||||
Sponsor Name:UZLeuven | |||||||||||||
Full Title: Prospective Randomised Double-blind Sham Study on the Use of Botox for the Treatment of Diffuse esophageal spasm | |||||||||||||
Medical condition: the effect of Botox on symptoms and manometry patterns in patients with diffuse esophageal spasm. | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-001853-41 | Sponsor Protocol Number: 57698 | Start Date*: 2018-09-19 | ||||||||||||||||||||||||||
Sponsor Name:Academic Medical Center | ||||||||||||||||||||||||||||
Full Title: Intensive endoscopic therapy versus conventional treatment for untreated benign anastomotic strictures after esophagectomy: a pilot and randomized controlled trial | ||||||||||||||||||||||||||||
Medical condition: Benign esophagogastric anastomotic strictures after esophagectomy | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: NL (Prematurely Ended) | ||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-005856-33 | Sponsor Protocol Number: AT10008 | Start Date*: 2007-02-13 | |||||||||||
Sponsor Name:The Department of Molecular Medicin and Surgery, P9:03, Karolinska Institutet | |||||||||||||
Full Title: Local Glucocorticoid Injektion in the Treatment of Benign Oesophageal Strictures, a Randomized Clinical Study | |||||||||||||
Medical condition: Patients with benign oesophageal strictures and symptoms where dilatation of the stricture is planned. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-006081-29 | Sponsor Protocol Number: Rimonaslok | Start Date*: 2008-10-21 | |||||||||||
Sponsor Name:UZLeuven | |||||||||||||
Full Title: INFLUENCE OF RIMONABANT ON LOWER ESOPHAGEAL FUNCTION IN HEALTHY VOLUNTEERS | |||||||||||||
Medical condition: none; this is a physiological study to investigate the influence of CB1 receptor antagonism by rimonabant (normally used for the treatment of obesity) on esophageal function, i.e. esophageal contr... | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-011174-15 | Sponsor Protocol Number: 2700/2008 | Start Date*: 2009-03-16 | ||||||||||||||||||||||||||
Sponsor Name:AZIENDA OSPEDALIERA PISANA | ||||||||||||||||||||||||||||
Full Title: PRE-OPERATIVE CHEMO-RADIOTHERAPIC TREATMENT IN ESOPHAGEAL AND GASTRO-ESOPHAGEAL JUNCTION ADENOCARCINOMA | ||||||||||||||||||||||||||||
Medical condition: ESOPHAGEAL AND GASTRO-ESOPHAGEAL JUNCTION ADENOCARCINOMA | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: IT (Prematurely Ended) | ||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-004633-24 | Sponsor Protocol Number: PCT | Start Date*: 2008-10-23 | |||||||||||||||||||||
Sponsor Name:Women's and Children's Hospital | |||||||||||||||||||||||
Full Title: A trial of position control therapy (PCT) for treatment of infantile gastro-oesophageal reflux | |||||||||||||||||||||||
Medical condition: gastro-oesophageal reflux related symptoms | |||||||||||||||||||||||
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Population Age: Preterm newborn infants, Newborns, Infants and toddlers, Under 18 | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: NL (Ongoing) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-004155-35 | Sponsor Protocol Number: A7421007 | Start Date*: 2005-12-01 | |||||||||||
Sponsor Name:Pfizer Limited | |||||||||||||
Full Title: A randomized, double blind, parallel group study to examine the effect of multiple doses of CJ-040,714 on distal esophageal acid exposure an patients with erosive gastro-esophageal reflux disease (... | |||||||||||||
Medical condition: Gastro-Esophageal Reflux Disease (GERD) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-004501-25 | Sponsor Protocol Number: D9120C00020 | Start Date*: 2006-12-18 | |||||||||||
Sponsor Name:AstraZeneca AB | |||||||||||||
Full Title: A double-blind, placebo controlled, randomized, two centre phase IIa pharmacodynamic cross-over study to assess the effect of AZD3355, 65 mg bid, on transient lower esophageal sphincter relaxations... | |||||||||||||
Medical condition: Gastroesophageal Reflux Disease (GERD) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) BE (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: 2010-018608-98 | Sponsor Protocol Number: D3830C00001 | Start Date*: 2010-06-09 | |||||||||||
Sponsor Name:AstraZeneca AB | |||||||||||||
Full Title: A double-blind, randomized, placebo-controlled, two-centre, phase IIa pharmacodynamic cross-over study to assess the effect of AZD2516 on the total number of reflux episodes in healthy male volunteers | |||||||||||||
Medical condition: Gastroesophageal Reflux Disease (GERD) | |||||||||||||
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Population Age: Adults | Gender: Male | ||||||||||||
Trial protocol: BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-003131-38 | Sponsor Protocol Number: DOPA2016 | Start Date*: 2017-06-23 |
Sponsor Name:TARGID, KU Leuven | ||
Full Title: The effect of chlorpromazine (Largactil), a dopamine type 2-(D2-) receptor antagonist, on esophageal sensitivity in healthy volunteers: a randomized, double-blind, placebo-controlled study | ||
Medical condition: Increased esophageal sensitivity in refractory gastro-esophageal reflux disease | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: BE (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: (No results available) |
EudraCT Number: 2020-005787-58 | Sponsor Protocol Number: eCaEP2021 | Start Date*: 2021-05-12 | |||||||||||
Sponsor Name:Michael Patrick | |||||||||||||
Full Title: Endoscopic assisted Calcium electroporation in esophageal cancer – a safety study | |||||||||||||
Medical condition: Esophageal cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
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: 2015-005556-10 | Sponsor Protocol Number: CA209-577 | Start Date*: 2016-05-24 | ||||||||||||||||||||||||||||||||||||
Sponsor Name:Bristol-Myers Squibb International Corporation | ||||||||||||||||||||||||||||||||||||||
Full Title: A Randomized, Multicenter, Double Blind, Phase III Study of Adjuvant Nivolumab or Placebo in Subjects with Resected Esophageal, or Gastroesophageal Junction Cancer | ||||||||||||||||||||||||||||||||||||||
Medical condition: Subjects with resected adenocarcinoma or squamous cell carcinoma esophageal or gastroesophageal junction cancer | ||||||||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||
Trial protocol: HU (Completed) ES (Ongoing) CZ (Trial now transitioned) GB (GB - no longer in EU/EEA) IE (Trial now transitioned) DE (Trial now transitioned) BE (Trial now transitioned) DK (Trial now transitioned) NL (Trial now transitioned) RO (Trial now transitioned) FR (Trial now transitioned) IT (Prematurely Ended) | ||||||||||||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-006647-31 | Sponsor Protocol Number: ASSO OE-1 | Start Date*: 2007-08-03 | |||||||||||
Sponsor Name:The Austrian Society of Surgical Oncology (ACO-ASSO) | |||||||||||||
Full Title: p53-Adjusted Neoadjuvant Chemotherapy for potentially resectable Oesophageal Cancer "pANCHO". | |||||||||||||
Medical condition: Interaction between a predictive marker and response to induction chemotherapy in patients with potentially resectable esophageal cancer Predictive Marker Trial | |||||||||||||
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Population Age: | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Ongoing) | |||||||||||||
Trial results: (No results available) |
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: 2008-002646-35 | Sponsor Protocol Number: M0003-C101 | Start Date*: 2008-08-06 | |||||||||||
Sponsor Name:Movetis NV | |||||||||||||
Full Title: A prospective phase 1, single-dose, open-label, multi-centre clinical trial to evaluate the pharmacokinetics and safety of M0003 in young children aged between 1 and 36 months. | |||||||||||||
Medical condition: Intended indication for product under development: Infant gastro-oesophageal reflux disease (GORD) | |||||||||||||
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Population Age: Infants and toddlers, Children, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) NL (Not Authorised) GB (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
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 |
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