- Trials with a EudraCT protocol (540)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (10)
540 result(s) found for: Endoscopy.
Displaying page 1 of 27.
EudraCT Number: 2011-005622-21 | Sponsor Protocol Number: OC002G | Start Date*: 2012-02-28 |
Sponsor Name:Clinical Research Centre, Hvidovre University Hospital | ||
Full Title: Clinical Trials with bupivacain lozenge as local anaesthesia under upper gastrointestinal endoscopy | ||
Medical condition: Discomfort during upper gastrointestinal endoscopy | ||
Disease: | ||
Population Age: Elderly | Gender: Male, Female | |
Trial protocol: DK (Completed) | ||
Trial results: View results |
EudraCT Number: 2009-010383-42 | Sponsor Protocol Number: PCSA/Remi2009 | Start Date*: 2009-02-19 | |||||||||||
Sponsor Name:OSPEDALE S. RAFFAELE | |||||||||||||
Full Title: Comparison between two different dosages of remifentanil administered by a patient controlled tecnique (PCSA) for diagnostic and andoscopich procedures. | |||||||||||||
Medical condition: patients affected by patologies to be submitted to endoscopic investigation | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-005528-13 | Sponsor Protocol Number: 30112012 | Start Date*: 2014-06-17 | |||||||||||
Sponsor Name:Helsinki University Hospital | |||||||||||||
Full Title: Comparison of Novel Articaine Lozenge Versus Placebo for Upper Gastrointestinal Endoscopy in Adults. A Randomized Double-blinded Controlled Study | |||||||||||||
Medical condition: Patients who undergo esophagogastroduodenoscopy procedure for a first time | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Completed) | |||||||||||||
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 |
EudraCT Number: 2005-004423-19 | Sponsor Protocol Number: CF/01 | Start Date*: 2005-12-06 |
Sponsor Name:The North West London Hospitals NHS Trust, Northwick Park Hospital | ||
Full Title: A randomised study of the optimal bowel preparation for routine Capsule endoscopy using Citramag and Senna or Metoclopramide. | ||
Medical condition: Investigation of suspected small bowel disease by Capsule Endoscopy | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2021-000985-14 | Sponsor Protocol Number: VICAPEND | Start Date*: 2021-03-23 | |||||||||||
Sponsor Name:Universitary Hospital Príncipe de Asturias | |||||||||||||
Full Title: Valuation of visualization quality of mucous membrane and diagnostic yield of small bowel capsule endoscopy using different bowel preparations clinical trial | |||||||||||||
Medical condition: Obscure gastrointestinal bleeding. Inflammatory bowel disease as Crohn's disease. Tumors of the small intestine. Hereditary polyposis syndrome (familial adenomatous polyposis or Peutz-Jeghers Syndr... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-003339-39 | Sponsor Protocol Number: EHDA-01 | Start Date*: 2017-05-03 | |||||||||||
Sponsor Name:JOSÉ MARÍA PALAZÓN AZORÍN | |||||||||||||
Full Title: A randomized, controlled and double-blind trial of intravenous azithromycin versus intravenous erythromycin as a single dose prior to endoscopy in upper gastrointestinal bleeding | |||||||||||||
Medical condition: Upper gastrointestinal haemorrhage | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-000573-37 | Sponsor Protocol Number: SHP647-303 | Start Date*: 2018-03-13 | |||||||||||
Sponsor Name:Shire Human Genetic Therapies, Inc. | |||||||||||||
Full Title: A Phase 3 Randomized, Double-blind, Placebo controlled, Parallel group Efficacy and Safety Study of SHP647 as Maintenance Therapy in Subjects With Moderate to Severe Ulcerative Colitis (FIGARO UC 303) | |||||||||||||
Medical condition: Ulcerative colitis | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IE (Completed) GB (GB - no longer in EU/EEA) DE (Completed) AT (Completed) LT (Completed) CZ (Completed) NL (Completed) SK (Completed) BG (Completed) GR (Completed) PL (Completed) BE (Completed) ES (Prematurely Ended) PT (Completed) HU (Completed) EE (Completed) HR (Completed) IT (Completed) RO (Completed) | |||||||||||||
Trial results: View results |
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: 2016-000406-11 | Sponsor Protocol Number: NL56591.078.16 | Start Date*: 2016-04-14 |
Sponsor Name:Erasmus University Medical Center | ||
Full Title: The influence of electroencephalographic Narcotrend Index™ - guidance of propofol administration on recovery from procedural sedation for gastrointestinal endoscopy in children between 1 and 12 years | ||
Medical condition: There is no specific medical condition under investigation | ||
Disease: | ||
Population Age: Children, Under 18 | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2013-002122-23 | Sponsor Protocol Number: NL44307.078.13 | Start Date*: 2013-07-11 |
Sponsor Name:Erasmus University Medical Center | ||
Full Title: The influence of electroencephalographic Narcotrend Index™- guidance of of propofol administration on recovery from procedural sedation for gastrointestinal endoscopy in paediatric patients | ||
Medical condition: There is no medical condition which is under investigation. Paediatric patients, scheduled for gastrointestinal endoscopy under procedural sedation are eligible for inclusion. Depth of sedation wil... | ||
Disease: | ||
Population Age: Adolescents, Under 18 | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2021-002537-41 | Sponsor Protocol Number: 20170104 | Start Date*: 2022-01-06 | |||||||||||
Sponsor Name:Amgen Inc. | |||||||||||||
Full Title: A Phase 2, Dose-finding, Randomized, Double-blind, Placebo-controlled, Multicenter Study to Evaluate the Safety and Efficacy of Efavaleukin Alfa Induction Therapy in Subjects with Moderately to Sev... | |||||||||||||
Medical condition: Moderate to Severe Active Ulcerative Colitis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Trial now transitioned) DK (Trial now transitioned) NL (Trial now transitioned) DE (Trial now transitioned) HU (Trial now transitioned) FI (Trial now transitioned) BG (Trial now transitioned) IT (Trial now transitioned) GR (Trial now transitioned) ES (Ongoing) BE (Trial now transitioned) RO (Trial now transitioned) SK (Trial now transitioned) LV (Trial now transitioned) FR (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
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: 2013-003187-31 | Sponsor Protocol Number: GN09CA403 | Start Date*: 2015-03-19 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Sponsor Name:NHS Greater Glasgow & Clyde | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Full Title: Misoprostol for the Healing of Small Bowel Ulceration in Patients with Obscure Blood Loss while Taking Low-Dose Aspirin or Non-Steroidal Anti-inflammatory Drugs [MASTERS Trial] | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Medical condition: Small bowel ulcers associated with iron deficiency anaemia or obscure blood loss in patients using aspirin or non-steroidal anti-inflammatory drugs | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial protocol: GB (Completed) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2018-003303-19 | Sponsor Protocol Number: RSJ10201 | Start Date*: 2019-03-15 | |||||||||||
Sponsor Name:Reistone Biopharma Company Limited | |||||||||||||
Full Title: A Phase II randomized, placebo controlled, double-blind, 4 arms dose-ranging study to evaluate the efficacy and safety of SHR0302 compared to placebo in patients with moderate to severe active Croh... | |||||||||||||
Medical condition: Crohn’s Disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: PL (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-001340-19 | Sponsor Protocol Number: NLROW.1012.15 | Start Date*: 2016-07-21 |
Sponsor Name:Radboud University Medical Center | ||
Full Title: An uncontrolled, pilot-study assessing the efficacy of octreotide LAR to decrease transfusion requirements and endoscopy frequency in patients with Rendu-Osler-Weber and gastrointestinal bleeding | ||
Medical condition: Patients with Rendu-Osler-Weber disease (which is also called: Hereditary hemorrhagic telangiectasia) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2011-005704-15 | Sponsor Protocol Number: ATF-EGD001 | Start Date*: 2012-01-02 |
Sponsor Name:Hospital Universitario Infanta Cristina | ||
Full Title: Usefulness of lidocaine as topical pharyngeal anaesthesia in esophagogastroduodenoscopy under sedation with propofol | ||
Medical condition: Propofol´s mean dosage in routinely esophagogastroduodenoscopy with and without topical pharyngeal anaesthesia with lidocaine. Variation between the patient´s groups in side effects and endoscopist... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Completed) | ||
Trial results: View results |
EudraCT Number: 2021-006617-11 | Sponsor Protocol Number: 122021 | Start Date*: 2022-06-07 | ||||||||||||||||
Sponsor Name:Region Nordjylland | ||||||||||||||||||
Full Title: A Randomised controlled trial to compare efficacy and tolerability of Plenvu® and Picoprep® as cleansing agents before colonoscopy | ||||||||||||||||||
Medical condition: The trial is about comparing the efficacy of Plenvu with Picoprep. Both are bowel cleansing agents prior to colonoscopy. The patients to be examined are all referred to exclude colorectal cancer di... | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DK (Trial now transitioned) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-000319-41 | Sponsor Protocol Number: RPC01-3101 | Start Date*: 2015-09-18 | |||||||||||
Sponsor Name:Celgene International II Sàrl (CIS II) | |||||||||||||
Full Title: A Phase 3, Multicenter, Randomized, Double-blind, Placebo-controlled Trial of Oral RPC1063 as Induction and Maintenance Therapy for Moderate to Severe Ulcerative Colitis | |||||||||||||
Medical condition: ulcerative colitis | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) SK (Completed) HU (Completed) CZ (Completed) NL (Completed) GB (Completed) BE (Completed) BG (Completed) PL (Completed) HR (Completed) LV (Completed) AT (Completed) GR (Completed) ES (Prematurely Ended) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-005694-23 | Sponsor Protocol Number: CB-17-01/05 | Start Date*: 2011-12-20 | |||||||||||||||||||||
Sponsor Name:COSMO TECHNOLOGIES LTD | |||||||||||||||||||||||
Full Title: Polyp detection rate after single oral dose of methylene blue MMX(R) modified release tablets administered to subjects undergoing outpatients colonoscopy | |||||||||||||||||||||||
Medical condition: patients scheduled for the screening or surveillance colonoscopy and meeting the joint guideline from the American Cancer Society, the US Multi-Society Task Force on Colorectal Cancer and the Ameri... | |||||||||||||||||||||||
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Population Age: Newborns, Infants and toddlers, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: IT (Completed) | |||||||||||||||||||||||
Trial results: (No results available) |
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