- Trials with a EudraCT protocol (102)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (4)
102 result(s) found for: Anastomosis.
Displaying page 1 of 6.
EudraCT Number: 2007-003006-98 | Sponsor Protocol Number: PROT-TISSUCOL-001 | Start Date*: 2007-07-16 | |||||||||||
Sponsor Name:Cirugía General II. Hospital General Universitario “Gregorio Marañón” | |||||||||||||
Full Title: ESTUDIO FASE IV, UNICENTRICO, ALEATORIZADO, SIMPLE CIEGO, CONTROLADO, COMPARATIVO DE DOS GRUPOS PARALELOS PARA EVALUAR LA EFICACIA DE TISSUCOL DUO (ADHESIVO BIOLOGICO A BASE DE FIBRINA) EN LA PREVE... | |||||||||||||
Medical condition: Defectos de cicatrización (fístulas, dehiscencias y fugas subclínicas) en la(s) anastomosis(s) de tubo digestivo de alto riesgo: Las anastomosis consideradas de alto riesgo son: 1. Anastomosis rect... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-001778-12 | Sponsor Protocol Number: HUGTP-CIR-FIBRIN-GLUE-01 | Start Date*: 2019-04-15 | |||||||||||||||||||||
Sponsor Name:Fundació Institut de Recerca en Ciències de la Salut Germans Trias i Pujol | |||||||||||||||||||||||
Full Title: USE OF A FIBRINE ADHESIVE TO REDUCE THE DEHISCENCE OF ESOFAGOYEYUNAL ANASTOMOSIS IN TOTAL GASTRECTOMIES BY CANCER: RANDOMIZED AND MULTICENTRIC STUDY. | |||||||||||||||||||||||
Medical condition: The dehiscence of the esophagojejunal anastomosis after a total gastrectomy in patients with gastric adenocarcinoma | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-007254-62 | Sponsor Protocol Number: TC-029-IM | Start Date*: 2008-07-01 |
Sponsor Name:Nycomed Danmark ApS | ||
Full Title: Non-randomised, open, multi-center trial evaluating feasibility and safety of TachoSil application on a colorectal anastomosis. | ||
Medical condition: The scope of this trial is to evaluate if it is possible to apply TachoSil around colorectal anastomosis and evaluate its feasibility in future clinical trials. Therefore the only focus is on the v... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Completed) DE (Completed) GB (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2011-005479-17 | Sponsor Protocol Number: 400-11-002 | Start Date*: 2012-05-02 |
Sponsor Name:Ethicon Inc., a Johnson & Johnson Co. | ||
Full Title: A Single Blind, Randomized, Controlled Study to Evaluate the Safety and Effectiveness of EVICEL® as an Adjunct to Gastrointestinal Anastomosis Techniques | ||
Medical condition: Gastrointestinal Anastomosis Leak | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) BE (Completed) | ||
Trial results: View results |
EudraCT Number: 2005-002912-73 | Sponsor Protocol Number: AL-JVC-05-01 | Start Date*: 2005-08-02 |
Sponsor Name:University Hospitals Leuven | ||
Full Title: An Open Label Evaluation of Efficacy and Safety of Posterior Juxtascleral Administrations of 15 mg Anecortave Acetate for Depot Suspension Combined with Verteporfin Therapy in Patients with Exudati... | ||
Medical condition: Age Related Macular Degeneration with Retino-choroidal Anastomosis | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2011-005749-10 | Sponsor Protocol Number: NL38212 | Start Date*: 2012-08-01 | ||||||||||||||||
Sponsor Name:University Medical Center Utrecht | ||||||||||||||||||
Full Title: Safety and Feasibility of TachoSil®: Application on Esophageal Anastomoses. A non-randomized single center study. | ||||||||||||||||||
Medical condition: Anastomotic leakage | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: NL (Ongoing) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-002369-17 | Sponsor Protocol Number: 2021-01 | Start Date*: 2021-07-22 |
Sponsor Name:GETAID | ||
Full Title: Management of moderate POstoperative recurrence in Crohn's disease: a randoMizEd contROLled trial, the POMEROL trial. | ||
Medical condition: Crohn's disease patients having an i2 endoscopic postoperative recurrence 6-12 months after ileocolonic anastomosis. | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: FR (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2005-005898-29 | Sponsor Protocol Number: RRK2962 | Start Date*: 2008-07-04 | |||||||||||||||||||||
Sponsor Name:University Hospital Birmingham | |||||||||||||||||||||||
Full Title: The effect of bosentan, a selective endothelin antagonist, on cardiovascular performance in patients with a Fontan circulation | |||||||||||||||||||||||
Medical condition: Patients with a Fontan circulation (that is they have had a Fontan operation for a functionally univentricular heart) | |||||||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: GB (Completed) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-002821-45 | Sponsor Protocol Number: AC-055H302 | Start Date*: 2019-03-05 | ||||||||||||||||
Sponsor Name:Actelion Pharmaceuticals Ltd | ||||||||||||||||||
Full Title: Prospective, multi-center, single-arm, open-label long-term study assessing the safety, tolerability, and effectiveness of macitentan in Fontan-palliated adult and adolescent subjects | ||||||||||||||||||
Medical condition: Congenital Heart Failure | ||||||||||||||||||
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Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: FR (Completed) DE (Completed) GB (GB - no longer in EU/EEA) DK (Completed) PL (Completed) CZ (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2014-000784-41 | Sponsor Protocol Number: 2014010113 | Start Date*: 2015-04-15 | |||||||||||
Sponsor Name:Department of Medicine and Endocrinology | |||||||||||||
Full Title: Amino acids in ileal pouch-anal anastomosis for ulcerative colitis: a randomized, double-blind placebo-controlled trial | |||||||||||||
Medical condition: Ileal pouch-anal anastomosis for ulcerative colitis | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-000639-29 | Sponsor Protocol Number: ABCSG_P00 | Start Date*: 2013-03-27 | ||||||||||||||||
Sponsor Name:ABCSG (Austrian Breast & Colorectal Cancer Study Group) | ||||||||||||||||||
Full Title: A prospective, open, randomized, academic phase II, two-arm trial evaluating the effect of fibrin-coated collagen (TachoSil®) on postoperative pancreatic leakage and fistula formation from the panc... | ||||||||||||||||||
Medical condition: pancreatic surgery - evaluation of the effect of fibrin-coated collagen | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: AT (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2009-012994-37 | Sponsor Protocol Number: TACO1 | Start Date*: 2009-12-13 | |||||||||||
Sponsor Name:UNIVERSITA` CAMPUS BIOMEDICO | |||||||||||||
Full Title: RANDOMISED PROSPECTIVE TRIAL: PREVENTION OF PANCREATIC FISTULA AFTER PANCREATICO-DUODENECTOMY USING BIOLOGICAL SEALANT | |||||||||||||
Medical condition: - patients underwent pancreatico-duodenectomy with pancreatico-jejunal anastomosis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-003320-23 | Sponsor Protocol Number: AC-055H301 | Start Date*: 2017-10-11 | ||||||||||||||||
Sponsor Name:Actelion Pharmaceuticals Ltd | ||||||||||||||||||
Full Title: Prospective, multi-center, double-blind, randomized, placebo-controlled, parallel-group study assessing the efficacy and safety of macitentan in Fontan-palliated adult and adolescent subjects. | ||||||||||||||||||
Medical condition: Congenital Heart Failure | ||||||||||||||||||
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Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) DE (Completed) DK (Completed) FR (Completed) PL (Completed) IE (Completed) CZ (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2015-005527-12 | Sponsor Protocol Number: 55868 | Start Date*: 2016-12-02 |
Sponsor Name: | ||
Full Title: Sirolimus for the treatment of severe intestinal polyposis in patients with familial adenomatous polyposis (FAP); a pilot study | ||
Medical condition: Familial adenomatous polyposis | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: NL (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2007-005455-42 | Sponsor Protocol Number: IBD-ENDO-2008-1 | Start Date*: 2009-02-26 | |||||||||||
Sponsor Name:University Medical Center Utrecht | |||||||||||||
Full Title: ENDO ACE TRIAL Endoscopic Balloon Dilatation of stenotic ileocecal anastomosis in Crohn´s disease with or without additive local steroid injection and oral Budenofalk; a randomized controlled tri... | |||||||||||||
Medical condition: Crohn's disease. Patients with Crohn's disease with status after ileocecal resection. Stenotic ileocecal anastomosis with symptoms of obstruction. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-004814-21 | Sponsor Protocol Number: 2021/582 | Start Date*: 2022-06-14 | |||||||||||
Sponsor Name:CHU de Besançon | |||||||||||||
Full Title: Intraoperative indocyanine green fluorescence angiography in colorectal surgery to prevent anastomotic leakage: a single-blind phase III multicenter randomized controlled trial (intergroup FRENCH-G... | |||||||||||||
Medical condition: Anastomotic fistula during colorectal cancer surgery | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-000889-39 | Sponsor Protocol Number: 400-05-001 | Start Date*: 2005-06-28 |
Sponsor Name:OMRIX biopharmaceuticals Ltd | ||
Full Title: A Prospective, Randomized Controlled Study to Compare the Effects of a Fibrin Sealant(FS2) Versus Manual Compression on Haemostatic Efficacy During Vascular Surgical Procedures Utilising Polytetraf... | ||
Medical condition: Patients undergoing vascular surgical procedures will be included in this study. This will include patients with peripheral vascular disease and also patients with renal disease who require vascula... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2009-015136-14 | Sponsor Protocol Number: FP-0110-201 | Start Date*: 2009-11-20 | |||||||||||
Sponsor Name:FORMAC Pharmaceuticals NV | |||||||||||||
Full Title: Modified release metronidazole for the treatment of pouchitis after colectomy with ileo-anal pouch anastomosis for ulcerative colitis: a pharmacokinetic study | |||||||||||||
Medical condition: Pouchitis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2022-002536-32 | Sponsor Protocol Number: GREEN-EX | Start Date*: 2023-07-06 | |||||||||||||||||||||
Sponsor Name:FONDAZIONE POLICLINICO UNIVERSITARIO AGOSTINO GEMELLI IRCCS UNIVERSITA' CATTOLICA DEL SACRO CUORE | |||||||||||||||||||||||
Full Title: Indocyanine green to assess vascularity of ileal conduit anastomosis and regulate ureteral resection margins during pelvic exenteration for recurrent/persistent gynecological cancer. A pilot study | |||||||||||||||||||||||
Medical condition: Patients with gynecological cancers undergoing pelvic exenteration | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||||||||||||
Trial protocol: IT (Trial now transitioned) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2022-001139-98 | Sponsor Protocol Number: IC2021-07 | Start Date*: 2022-06-13 | ||||||||||||||||
Sponsor Name:Institut Curie | ||||||||||||||||||
Full Title: Opioid-Free versus Opioid-Based Anaesthesia for secondary free-flap reconstruction surgery of the breast: A phase III multicentric randomized controlled study | ||||||||||||||||||
Medical condition: Anaesthesia during secondary free flap reconstruction surgery of the breast. | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Female | |||||||||||||||||
Trial protocol: FR (Trial now transitioned) | ||||||||||||||||||
Trial results: (No results available) |
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