- Trials with a EudraCT protocol (86)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
86 result(s) found for: Therapeutic endoscopy.
Displaying page 2 of 5.
EudraCT Number: 2012-002356-16 | Sponsor Protocol Number: SUS2012CMR01 | Start Date*: 2012-11-27 | ||||||||||||||||
Sponsor Name:Stavanger University Hospital | ||||||||||||||||||
Full Title: Pre-emptive local anaesthesia in gynecological laparoscopy. | ||||||||||||||||||
Medical condition: Gynecological patients referred for elective day-care laparoscopic surgery. | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Female | |||||||||||||||||
Trial protocol: NO (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-003986-33 | Sponsor Protocol Number: APD334-302 | Start Date*: 2019-07-01 | ||||||||||||||||
Sponsor Name:Arena Pharmaceuticals Inc. | ||||||||||||||||||
Full Title: A Phase 3, Randomized, Double Blind, Placebo Controlled, 12 Week Study to Assess the Efficacy and Safety of Etrasimod in Subjects with Moderately to Severely Active Ulcerative Colitis | ||||||||||||||||||
Medical condition: Ulcerative Colitis | ||||||||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: SK (Completed) BE (Completed) NL (Completed) GB (GB - no longer in EU/EEA) EE (Completed) DE (Completed) AT (Completed) CZ (Completed) FR (Completed) DK (Completed) LT (Completed) BG (Completed) PT (Completed) LV (Prematurely Ended) HU (Completed) PL (Completed) HR (Completed) ES (Ongoing) IT (Completed) RO (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2012-003342-33 | Sponsor Protocol Number: STH16359 | Start Date*: 2012-09-28 | |||||||||||
Sponsor Name:Sheffield Teaching Hospitals NHS Foundation Trust | |||||||||||||
Full Title: Optimising the use of Entonox during screening colonoscopy: an open randomised controlled trial | |||||||||||||
Medical condition: Colonoscopy | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-001942-28 | Sponsor Protocol Number: APD334-003 | Start Date*: 2015-12-10 | |||||||||||
Sponsor Name:Arena Pharmaceuticals, Inc. | |||||||||||||
Full Title: A Phase 2, Randomized, Double-Blind, Placebo-Controlled, Parallel Group, Multi-Center Study to Investigate the Safety and Efficacy of APD334 in Patients with Moderately to Severely Active Ulcerativ... | |||||||||||||
Medical condition: Ulcerative colitis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Completed) GB (Completed) ES (Completed) DE (Completed) LV (Completed) HU (Completed) LT (Completed) FR (Completed) PL (Completed) BG (Completed) BE (Completed) AT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-001182-21 | Sponsor Protocol Number: APC-01-2021 | Start Date*: 2021-06-21 | |||||||||||
Sponsor Name:University Hospital Puerta de Hierro Majadahonda, Madrid, Spain | |||||||||||||
Full Title: RANDOMIZED, UNICENTRIC, DOUBLE BLIND, PLACEBO-CONTROLLED TRIAL TO ASSESS THE EFFICACY OF PARACERVICAL ANESTHESIA FOR PAIN CONTROL DURING AN OFFICE HYSTEROSCOPY | |||||||||||||
Medical condition: Need to do an office Hysteroscopy for any reason | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2004-005018-35 | Sponsor Protocol Number: SAS-6/UCA | Start Date*: 2005-10-31 |
Sponsor Name:Dr. Falk Pharma GmbH | ||
Full Title: Randomized, single-blind, multicentre study to compare the efficacy and safety of once daily 1 g mesalazine suppositories versus three times daily 0.5 g mesalazine suppositories in patients with ac... | ||
Medical condition: acute ulcerative proctitis | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2018-003985-15 | Sponsor Protocol Number: APD334-301 | Start Date*: 2019-06-21 | ||||||||||||||||
Sponsor Name:Arena Pharmaceuticals Inc. | ||||||||||||||||||
Full Title: A Phase 3, Randomized, Double-Blind, Placebo-Controlled, 52-Week Study to Assess the Efficacy and Safety of Etrasimod in Subjects with Moderately to Severely Active Ulcerative Colitis | ||||||||||||||||||
Medical condition: Ulcerative Colitis | ||||||||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: SK (Completed) BE (Completed) DE (Completed) LV (Completed) AT (Completed) NL (Completed) LT (Completed) PT (Completed) FR (Completed) EE (Completed) HU (Completed) DK (Completed) CZ (Completed) PL (Completed) BG (Completed) ES (Ongoing) HR (Completed) IT (Completed) RO (Completed) | ||||||||||||||||||
Trial results: View results |
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: 2013-000634-35 | Sponsor Protocol Number: CB-17-01/08 | Start Date*: 2013-05-11 | |||||||||||
Sponsor Name:Cosmo Technologies Ltd. | |||||||||||||
Full Title: Effect of oral administration of Methylene Blue MMX® tablets on double-stranded DNA damage assessed by γH2AX analysis of colon biopsy samples | |||||||||||||
Medical condition: Out-patients of both sexes scheduled for a screening or surveillance colonoscopy and identified as having the clinical requirement for a second colonoscopy within 2 weeks of the initial colonoscopy. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-001976-48 | Sponsor Protocol Number: IM011023 | Start Date*: 2018-08-23 | ||||||||||||||||
Sponsor Name:Bristol-Myers Squibb International Corporation | ||||||||||||||||||
Full Title: A Phase 2 Randomized, Double-Blind, Placebo-Controlled Study of the Safety and Efficacy of BMS-986165 in Subjects with Moderate to Severe Crohn's Disease | ||||||||||||||||||
Medical condition: Crohn's Disease | ||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) HU (Completed) FR (Completed) ES (Ongoing) PL (Completed) DE (Completed) DK (Prematurely Ended) PT (Completed) NL (Completed) BE (Completed) IT (Completed) RO (Ongoing) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2016-000390-20 | Sponsor Protocol Number: TOP1288-TV-02 | Start Date*: 2016-06-10 | |||||||||||
Sponsor Name:TOPIVERT Pharma Limited | |||||||||||||
Full Title: A Phase 2a, Randomised, Double-Blind, Placebo-Controlled Study to Evaluate the Safety/Tolerability and Efficacy of TOP1288 200 mg Rectal Solution Once Daily for 4 Weeks in Symptomatic Ulcerative Co... | |||||||||||||
Medical condition: Symptomatic Ulcerative Colitis Patients with Moderate Disease Activity | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) HU (Completed) LV (Completed) PL (Completed) LT (Completed) BG (Completed) CZ (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-002428-17 | Sponsor Protocol Number: 2013052044 | Start Date*: 2013-10-04 | |||||||||||
Sponsor Name:Gastroenheden D, Herlev Hospital | |||||||||||||
Full Title: Nurse Administered Propofol Sedation vs combined sedation with midazolam/fentanil for colonoscopy in patients with IBD. A randomised controlled trial of satisfaction and adhearence to treatment pro... | |||||||||||||
Medical condition: Satisfaction with sedation during colonoscopy in patients with inflammatory bowel disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-005215-16 | Sponsor Protocol Number: CHUB-MentalRecup001 | Start Date*: 2015-02-13 | |||||||||||
Sponsor Name:CHU Brugmann | |||||||||||||
Full Title: A psychomotor recuperation study after deep sedation for colonoscopy between target controlled and manual titration of propofol. | |||||||||||||
Medical condition: Ambulatory colonoscopy with sedation by target controlled infusion or manual titration of propofol. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-000869-36 | Sponsor Protocol Number: CSPT-END-DIG-2012 | Start Date*: 2013-06-28 | |||||||||||
Sponsor Name:Fundació Parc Taulí | |||||||||||||
Full Title: Multidisciplinary approach versus conventional approach in colonic preparation of hospitalized patients. A randomized controlled trial | |||||||||||||
Medical condition: Colon preparation for colonoscopy | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-001369-25 | Sponsor Protocol Number: HPT30/J/17 | Start Date*: 2018-03-19 |
Sponsor Name:INFAI Institut für biomedizinische Analytik und NMR Imaging GmbH | ||
Full Title: The Sensitivity and Specificity of the Modified Helicobacter Test INFAI Using New Test Meal with 13C-Urea Breath Test in Helicobacter Pylori Positive and Negative Patients with Dyspepsia and GERD T... | ||
Medical condition: Diagnosis of Helicobacter pylori infection for patients taking proton pump inhibitors (PPI) with one day break of medication instead of two weeks prior to the test | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2015-002025-19 | Sponsor Protocol Number: RPC01-2201 | Start Date*: 2015-12-30 | |||||||||||||||||||||
Sponsor Name:Celgene International II Sarl (CISII) awholly owned subsidiary of Celgene Corporation | |||||||||||||||||||||||
Full Title: A Phase 2, Multi-Center, Open-Label Induction Trial with Extension Period to Assess Endoscopic Improvement and Changes in Intestinal and Serum Biomarkers in Patients with Moderately to Severely Act... | |||||||||||||||||||||||
Medical condition: Moderately to Severely Active Crohn's Disease | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: HU (Completed) PL (Completed) IT (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2020-004957-62 | Sponsor Protocol Number: ET20-093 | Start Date*: 2021-09-09 |
Sponsor Name:Centre Léon Bérard | ||
Full Title: Immunotherapy in MSI/dMMR Tumors in perioperative setting | ||
Medical condition: MSI/dMMR tumors or EBV+ gastric cancer | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FR (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2020-000878-15 | Sponsor Protocol Number: NL72398.041.19 | Start Date*: 2020-04-15 |
Sponsor Name:University Medical Center Utrecht | ||
Full Title: Sentinel node Navigation surgery in early esophageal Adenocarcinoma Patients with lymph node involvement: SNAP-IV study | ||
Medical condition: Esophageal adenocarcinoma | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2008-005747-42 | Sponsor Protocol Number: 1255/08 | Start Date*: 2009-02-03 | |||||||||||
Sponsor Name:POLICLINICO UNIVERSITARIO AGOSTINO GEMELLI | |||||||||||||
Full Title: Efficacy of a medical product containing sorbitol, simethicone and citrate potassium, in comparison with domperidone in patients affected by disfunctional dyspepsia: randomized monocentric cross-ov... | |||||||||||||
Medical condition: dysfunctional dyspepsia | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-003257-16 | Sponsor Protocol Number: CitraFleet_H-2018 | Start Date*: 2018-11-07 | |||||||||||
Sponsor Name:Goodwill Pharma Kft. | |||||||||||||
Full Title: Efficacy, Safety and Tolerability of CitraFleet, a New Bowel Cleansing Agent – a Prospective, Single-Center, Single-Group Phase IV Study | |||||||||||||
Medical condition: Colonoscopy bowel preparation | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) | |||||||||||||
Trial results: View results |
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