- Trials with a EudraCT protocol (32)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
32 result(s) found for: Gastroscopy.
Displaying page 1 of 2.
EudraCT Number: 2009-011618-12 | Sponsor Protocol Number: a002c | Start Date*: 2009-06-18 | |||||||||||
Sponsor Name:Helsinki Central university Hospital | |||||||||||||
Full Title: Pharyngeal anaestesia with articaine:does it reduce surgical stress in gastroscopy? | |||||||||||||
Medical condition: Pharyngeal anesthesia for gastroscopy | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-002242-20 | Sponsor Protocol Number: ENT1 | Start Date*: 2013-02-04 |
Sponsor Name:Royal Bournemouth & Christchurch Hospitals NHS Foundation Trust | ||
Full Title: A single-centre, randomised controlled study of Entonox versus midazolam in upper GI endoscopy. | ||
Medical condition: Any patient with symptoms requiring investigation with a gastroscopy. There is no single condition to which this would apply. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (GB - no longer in EU/EEA) | ||
Trial results: View results |
EudraCT Number: 2018-000026-54 | Sponsor Protocol Number: 18662008 | Start Date*: 2018-09-12 |
Sponsor Name:Medicinkliniken, Sjukhuset Lidköping | ||
Full Title: A comparison of sedatives used during gastroscopy, alfentanil vs midazolam | ||
Medical condition: Sedative effect during gastroscopy | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: SE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2015-000923-10 | Sponsor Protocol Number: LIDOGTC | Start Date*: 2015-10-29 | |||||||||||
Sponsor Name:BASQUE HEALTH SYSTEM | |||||||||||||
Full Title: Evaluation of the efficacy and safety of administering lidocaine spray in oesophagogastroduodenoscopies: A randomized clinical trial. | |||||||||||||
Medical condition: Elective gastroscopy | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-005747-23 | Sponsor Protocol Number: 10 | Start Date*: 2021-05-05 |
Sponsor Name:Nemocnice Agel Ostrava-Vítkovice a.s. | ||
Full Title: Use of mucolytic solution before gastroscopy, double-blind, randomized study | ||
Medical condition: Visibility mucosal score during upper endoscopy after administration of mucolytic solution | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: CZ (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2016-003739-40 | Sponsor Protocol Number: 59153 | Start Date*: 2017-03-06 |
Sponsor Name:AMC Amsterdam | ||
Full Title: The effect of Iberogast on heartburn in patients with dyspepsia | ||
Medical condition: Dyspepsia (according to the Rome III criteria) with heartburn. Upper gastro-intestinal causes of the complaints excluded via gastroscopy | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: NL (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2012-002183-27 | Sponsor Protocol Number: T-019 | Start Date*: 2013-04-03 | |||||||||||
Sponsor Name:Hammersmith Medicines Research | |||||||||||||
Full Title: Can netazepide eradicate the inflammatory response of the gastric mucosa to H. pylori infection? | |||||||||||||
Medical condition: Gastritis associated with H. pylori infection | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-002462-12 | Sponsor Protocol Number: NL70085.058.19 | Start Date*: 2019-10-22 |
Sponsor Name:Leiden Universitair Medisch Centrum | ||
Full Title: Imaging tumor angiogenesis using [18F]-PSMA-1007 PET/CT in patients with colon and gastric cancer. | ||
Medical condition: Colon and gastric cancer patients | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2015-003512-20 | Sponsor Protocol Number: IN11004 | Start Date*: 2016-05-09 | |||||||||||
Sponsor Name:Intec Pharma, Ltd. | |||||||||||||
Full Title: A Phase III, Multicenter, Randomized, Double-Blind, Double-Dummy, Active-Controlled Study Comparing the Efficacy and Safety of Gastric Retentive, Controlled Release Accordion Pill™ Carbidopa/Levodo... | |||||||||||||
Medical condition: Parkinson's Disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Prematurely Ended) GB (Completed) SK (Completed) ES (Completed) PL (Completed) IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-007420-26 | Sponsor Protocol Number: D9127C00002 | Start Date*: 2009-05-13 | |||||||||||
Sponsor Name:AstraZeneca AB | |||||||||||||
Full Title: A phase IIa, double-blind, randomized, 2-way cross-over study to evaluate the effect of a single dose of AZD1386 95 mg compared to placebo in a multimodal experimental pain model on esophageal sens... | |||||||||||||
Medical condition: Gastroesophageal Reflux Disease (GERD) is the intended indication | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Prematurely Ended) DK (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-021390-36 | Sponsor Protocol Number: buspar2010 | Start Date*: 2010-09-07 |
Sponsor Name:uzleuven | ||
Full Title: The Effect of Acute Intake of Oral Buspirone Hydrochloride on Esophageal Motility, Bolus Transit and Symptoms of Dysphagia, in Patients with Ineffective Esophageal Motility: A Pilot, Open-label, Si... | ||
Medical condition: Ineffective Esophageal Motility | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: View results |
EudraCT Number: 2016-002550-20 | Sponsor Protocol Number: AMIRA | Start Date*: 2017-07-17 |
Sponsor Name:University of Ulm | ||
Full Title: Allogeneic microbiota-reconstitution (AMR) for the Treatment of patients with diarrhea-predominant irritable bowel Syndrome (IBS-D) - the AMIRA trial | ||
Medical condition: diarrhea-predominant irritable bowel syndrome | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2015-001169-21 | Sponsor Protocol Number: S55731 | Start Date*: 2015-04-14 |
Sponsor Name:Catholic University Leuven | ||
Full Title: Acid pocket: Determination of position and aspiration | ||
Medical condition: Gastro-oesophageal reflux disease Healthy volunteers and patients with reflux disease who respond to PPI therapy and who partially respond to PPI therapy will be studied It is known, that after the... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2008-002106-19 | Sponsor Protocol Number: | Start Date*: 2008-07-10 |
Sponsor Name:Chelsea & Westminster NHS Foundation Trust | ||
Full Title: Remifentanil sedation for outpatient endoscopic procedures | ||
Medical condition: We are investigating the use of remifentanil for sedation in outpatient endoscopic procedures. It will be compared to 'current practice' sedation with midazolam and fentanyl. Patient who are due to... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2009-011979-76 | Sponsor Protocol Number: 253/09 | Start Date*: 2009-04-20 | ||||||||||||||||
Sponsor Name:POLICLINICO UNIVERSITARIO AGOSTINO GEMELLI | ||||||||||||||||||
Full Title: Effectiveness of acetylcysteine in rescue therapy for Helicobacter pylori infection. Pilot Study | ||||||||||||||||||
Medical condition: Duodenal and gastric ulcer recurrence with Helicobacter P. infection | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: IT (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-006887-12 | Sponsor Protocol Number: HEPACO | Start Date*: 2011-12-07 |
Sponsor Name:Institut de Recerca HSCSP | ||
Full Title: Randomized controlled trial to compare treatment with oral anticoagulation with vitamin K antagonists versus low molecular weight heparin (bemiparin) in patients with anticoagulation criteria and h... | ||
Medical condition: Patients with gastrointestinal bleeding are not candidates for endoscopic treatment with oral anticoagulant previously. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2009-011978-15 | Sponsor Protocol Number: 252/09 | Start Date*: 2010-02-22 | ||||||||||||||||
Sponsor Name:POLICLINICO UNIVERSITARIO AGOSTINO GEMELLI | ||||||||||||||||||
Full Title: Effectiveness of acetylcysteine in first line therapy to cure Helicobacter pylori. Pilot study. | ||||||||||||||||||
Medical condition: peptic, duodenal and gastric ulcer with Helicobacter pylori infection | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: IT (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-003347-10 | Sponsor Protocol Number: PXR-HDL | Start Date*: 2017-01-16 |
Sponsor Name:Oulu University Hospital, Internal Medicine Research Unit | ||
Full Title: The effects of PXR activation on HDL-cholesterol | ||
Medical condition: Healthy volunteers | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: FI (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2018-002509-78 | Sponsor Protocol Number: BOPPP | Start Date*: 2019-04-24 | ||||||||||||||||
Sponsor Name:Kings College Hospital NHS Foundation Trust | ||||||||||||||||||
Full Title: Beta-blockers Or Placebo for Primary Prophylaxis of oesophageal varices (BOPPP Trial). A blinded, UK multi-centre, clinical effectiveness and cost-effectiveness randomised controlled trial. | ||||||||||||||||||
Medical condition: Liver cirrhosis with small oesophageal varices | ||||||||||||||||||
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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: 2013-001097-24 | Sponsor Protocol Number: PHT/2013/01 | Start Date*: 2013-05-23 | |||||||||||
Sponsor Name:Portsmouth Hospitals NHS trust | |||||||||||||
Full Title: Use of N-Acetylcysteine (NAC) and Simeticone as a pre-endoscopic drink to improve mucosal visualisation during gastroscopy: A randomised controlled trial | |||||||||||||
Medical condition: Early gastrointestinal lesions in the upper gastrointestinal tract. Our study is not looking at the direct treatment of any particular condition, but the early detecton of lesions. When performin... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
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