- Trials with a EudraCT protocol (149)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (1)
149 result(s) found for: Endoscopic surgery.
Displaying page 1 of 8.
EudraCT Number: 2006-000047-26 | Sponsor Protocol Number: AN05-7301 | Start Date*: 2006-03-10 |
Sponsor Name:Leeds Teaching Hospitals NHS Trust | ||
Full Title: A randomized controlled trial of caudal epidural or intravenous fentanyl on the post-operative analgesia requirements after transurethral endoscopic resection of prostate, bladder neck or bladder t... | ||
Medical condition: Bladder spasm following endoscopic resection for: Bladder tumour Prostate hypertrophy Prostate cancer | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (GB - no longer in EU/EEA) | ||
Trial results: (No results available) |
EudraCT Number: 2009-017997-19 | Sponsor Protocol Number: AGO/2009/014 | Start Date*: 2010-08-25 |
Sponsor Name:Ghent University Hospital | ||
Full Title: Influence of oral doxycycline on wound healing after endonasal endoscopic sinus surgery for chronic rhinosinusitis with and without nasal polyposis: a double-blind randomized placebo-controlled trial. | ||
Medical condition: Chronic rhinosinusitis | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2017-000867-34 | Sponsor Protocol Number: D001 | Start Date*: 2017-10-03 |
Sponsor Name:UMCG | ||
Full Title: ‘Immune protective anesthesia during endoscopic colon surgery to improve long-term survival’ | ||
Medical condition: We will include patients with colon cancer receiving endoscopic resection of tumor | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2016-000135-40 | Sponsor Protocol Number: 260585 | Start Date*: 2016-05-12 | ||||||||||||||||||||||||||
Sponsor Name:Zealand University Hospital, Department of Surgery | ||||||||||||||||||||||||||||
Full Title: Endoscopic assisted electrochemotherapy in addition to neoadjuvant treatment of locally advanced rectal cancer: a randomized clinical phase II trial. | ||||||||||||||||||||||||||||
Medical condition: Locally advanced rectal cancer | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: DK (Prematurely Ended) | ||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2022-003833-21 | Sponsor Protocol Number: TJT2301 | Start Date*: 2023-04-04 |
Sponsor Name:CHU of Liège | ||
Full Title: Is local injection of mesenchymal stem cells after endoscopic dilation safe and does it improve the outcome of intestinal stricture in patients with Crohn's disease? | ||
Medical condition: Crohn's disease patients with symptomatic intestinal stricture eligible to endoscopic dilatation | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2015-002102-37 | Sponsor Protocol Number: ORL-CENS-2015 | Start Date*: 2015-10-02 | ||||||||||||||||
Sponsor Name:Fundació Parc Taulí | ||||||||||||||||||
Full Title: Open randomized clinical trial to compare the efficacy of hypotensive anesthesia with clonidine or dexmedetomidine during endoscopic nasal surgery | ||||||||||||||||||
Medical condition: Nasosinusal endoscopic surgery in patients with chronic sinusitis and/or nasal polyposis | ||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: ES (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-002258-36 | Sponsor Protocol Number: RETIPC/01/17 | Start Date*: 2017-11-21 | |||||||||||
Sponsor Name:ALFASIGMA S.P.A. | |||||||||||||
Full Title: A Phase II, multicentre, double-blind, randomised, placebo-controlled study of Rifaximin delayed release 400 mg tablet: clinical efficacy and safety in the prevention of post-operative endoscopic C... | |||||||||||||
Medical condition: Post-operative endoscopic Crohn’s disease recurrence | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) BE (Prematurely Ended) ES (Prematurely Ended) NL (Prematurely Ended) PL (Completed) IT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-002865-40 | Sponsor Protocol Number: BIODYMF | Start Date*: 2015-12-08 |
Sponsor Name:Ghent University Hospital | ||
Full Title: Open label two treatment half-side comparative study to analyse difference in nasal bioavailability between MP29-02 and fluticasone propionate. | ||
Medical condition: Subjects who need to undergo septoplasty, septorhinoplasty or functional endoscopic sinus surgery unrelated to this study. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: View results |
EudraCT Number: 2018-004239-63 | Sponsor Protocol Number: NL68231.078.18 | Start Date*: 2019-08-23 | |||||||||||
Sponsor Name:Erasmus MC | |||||||||||||
Full Title: Botulinum toxin (BOTOX®) to prevent post-operative pancreatic fistula in patients who undergo distal pancreatectomy. PROFIT study. | |||||||||||||
Medical condition: Post-operative pancreatic fistula | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-002441-39 | Sponsor Protocol Number: D961DC00001 | Start Date*: 2005-11-07 | |||||||||||
Sponsor Name:AstraZeneca AB | |||||||||||||
Full Title: A randomised, double-blind, parallel-group, placebo controlled study of esomeprazole i.v. (bolus infusion of 80 mg followed by a continuous infusion of 8 mg per hour) administered for 72 hours to a... | |||||||||||||
Medical condition: Gatrointestinal haemorrhages NEC. (Bleeding gastric or duodenal ulcer will be investigated). MedDRA classification code Level: HLGT = High Level Group Term. See below. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) FI (Completed) SE (Completed) NO (Completed) DK (Completed) ES (Completed) AT (Completed) DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-005965-18 | Sponsor Protocol Number: ORL-CENS-2012 | Start Date*: 2012-02-21 | ||||||||||||||||||||||||||
Sponsor Name:Fundació Parc Taulí | ||||||||||||||||||||||||||||
Full Title: Open randomized trial to compare the bleeding during endoscopic nasal surgery after hypotensive anesthesia with clonidine or remifentanil. | ||||||||||||||||||||||||||||
Medical condition: Nasosinusal endoscopic surgery in patients with chronic sinusitis and/or nasal polyposis | ||||||||||||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: ES (Completed) | ||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-005199-90 | Sponsor Protocol Number: RHB-104-04 | Start Date*: 2019-02-14 | |||||||||||
Sponsor Name:RedHill Biopharma Ltd. | |||||||||||||
Full Title: An Open Label Study to Assess the Efficacy and Safety of Fixed-Dose Combination RHB-104 in Subjects with Active Crohn’s Disease Despite 26 Weeks of Participation in the MAP US RHB-104-01 Study | |||||||||||||
Medical condition: Moderately to Severely Active Crohn's Disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SK (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2022-001752-42 | Sponsor Protocol Number: PRESTO | Start Date*: 2023-04-13 | ||||||||||||||||
Sponsor Name:Frankfurter Institut für Klinische Krebsforschung IKF GmbH | ||||||||||||||||||
Full Title: The PRESTO Trial- Organ preservation with durvalumab-based immunotherapy in combination with chemoradiation as definitive therapy for early stage, cT1 and cT2N0, esophageal adenocarcinoma with indi... | ||||||||||||||||||
Medical condition: T1-T2N0 esophageal adenocarcinoma including gastroesophageal junction (GEJ) with indication for radical surgery | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Trial now transitioned) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-000642-62 | Sponsor Protocol Number: M14-675 | Start Date*: 2019-06-13 | |||||||||||
Sponsor Name:AbbVie Deutschland GmbH & Co. KG | |||||||||||||
Full Title: M14-675, A Multicenter, Randomized, Double-Blind, Placebo-Controlled Induction Study to Evaluate the Efficacy and Safety of Upadacitinib (ABT-494) in Subjects with Moderately to Severely Active Ulc... | |||||||||||||
Medical condition: Ulcerative Colitis | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) LV (Completed) PT (Completed) FI (Completed) DE (Completed) GR (Completed) SE (Completed) GB (GB - no longer in EU/EEA) AT (Completed) CZ (Completed) LT (Completed) IE (Completed) BE (Completed) HU (Completed) ES (Completed) SK (Completed) PL (Completed) FR (Completed) HR (Completed) NO (Completed) IT (Completed) RO (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-005688-32 | Sponsor Protocol Number: CD-FNB | Start Date*: 2009-07-02 | |||||||||||
Sponsor Name:Univeristy Hospital Na Bulovce | |||||||||||||
Full Title: Biological therapy in the prevention of Crohn`s disease recurrence after resection in ileocecal region. | |||||||||||||
Medical condition: Prevention of Crohn`s disease recurrence after surgery in ileocecal region by postoperative application of infliximab (four infusions). | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-001723-12 | Sponsor Protocol Number: CSAI | Start Date*: 2013-10-07 | |||||||||||
Sponsor Name:Fundació Clínic per a la Recerca Biomèdica | |||||||||||||
Full Title: A randomized, double-blinded, placebo-controlled study on the effects of adalimumab intralesional intestinal strictures of Crohn's disease patients | |||||||||||||
Medical condition: Crohn disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-004545-34 | Sponsor Protocol Number: AT10001 | Start Date*: 2006-02-20 |
Sponsor Name:Unit of Esophageal and Gastric Research Dep. of Molecular Medicine and Surgery Karolinska Institutet | ||
Full Title: Can Angiotensin II type 1 Receptor Inhibitor Be Used to Lower the Amount of Lipase and Amylase Level after Endoscopic Retrograde Cholangio-Pancreatography? | ||
Medical condition: The clinical diagnosis of acute pancreatitis is set by a combination of symptoms (abdominal pain) and increased blood levels of pancreatic enzymes (i.e. amylase and lipase). The most common complic... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: SE (Completed) | ||
Trial results: View results |
EudraCT Number: 2015-000555-24 | Sponsor Protocol Number: 2015-100752 | Start Date*: 2016-06-16 |
Sponsor Name:Academic Medical Center Amsterdam | ||
Full Title: Randomized, Placebo-Controlled, Double-Blind, Multicenter Study to Determine the Efficacy and Safety of Vedolizumab in Prevention of Endoscopic Recurrence of Crohn's Disease in Patients with Ileo-c... | ||
Medical condition: Crohn's disease | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Completed) ES (Ongoing) FR (Ongoing) IT (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2022-002389-33 | Sponsor Protocol Number: CNTO1959CRD3007 | Start Date*: 2023-04-07 | |||||||||||
Sponsor Name:Janssen-Cilag International NV | |||||||||||||
Full Title: A Randomized, Double-blind, Placebo-controlled Study Evaluating the Safety and Efficacy of Guselkumab for the Treatment of Participants with Crohn’s Disease After Surgical Resection | |||||||||||||
Medical condition: Crohn’s Disease After Surgical Resection | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) IT (Prematurely Ended) ES (Prematurely Ended) HU (Prematurely Ended) BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-003238-96 | Sponsor Protocol Number: I6T-MC-AMBG | Start Date*: 2018-10-15 | |||||||||||
Sponsor Name:Eli Lilly and Company | |||||||||||||
Full Title: A PHASE 3, MULTICENTER, RANDOMIZED, DOUBLE-BLIND, PARALLEL-ARM, PLACEBO-CONTROLLED MAINTENANCE STUDY OF MIRIKIZUMAB IN PATIENTS WITH MODERATELY TO SEVERELY ACTIVE ULCERATIVE COLITIS (LUCENT 2) | |||||||||||||
Medical condition: Moderately to Severely Active Ulcerative Colitis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) GB (GB - no longer in EU/EEA) NL (Ongoing) LV (Completed) CZ (Completed) LT (Completed) ES (Completed) BE (Completed) HU (Completed) AT (Completed) SK (Completed) DK (Completed) HR (Completed) IT (Completed) RO (Ongoing) | |||||||||||||
Trial results: View results |
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