- Trials with a EudraCT protocol (22)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
22 result(s) found for: Pancreatectomy.
Displaying page 1 of 2.
| EudraCT Number: 2007-004004-12 | Sponsor Protocol Number: S245.3.124 | Start Date*: 2008-02-28 | ||||||||||||||||
| Sponsor Name:Solvay Pharmaceuticals GmbH | ||||||||||||||||||
| Full Title: A STUDY TO INVESTIGATE THE EFFECT OF PANCRELIPASE DELAYED RELEASE CAPSULES ON MALDIGESTION IN PATIENTS WITH EXOCRINE PANCREATIC INSUFFICIENCY DUE TO CHRONIC PANCREATITIS AND PANCREATECTOMY | ||||||||||||||||||
| Medical condition: Pancreatic enzyme replacement therapy is the cornerstone of nutritional management of pancreatic exocrine insufficiency (PEI) due to e.g. cystic fibrosis, chronic pancreatitis, partial or complete ... | ||||||||||||||||||
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| Population Age: Adults | Gender: Male, Female | |||||||||||||||||
| Trial protocol: BG (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2019-002461-35 | Sponsor Protocol Number: PREBOTPilot | Start Date*: 2019-12-06 | |||||||||||
| Sponsor Name:Ruprecht-Karls-University Heidelberg Medical Faculty represented by Universitätsklinikum Heidelberg and its acting Comm | |||||||||||||
| Full Title: Monocenter, randomized, controlled, open-label, phase-II clinical trial of PREoperative endoscopic injection of BOTulinum toxin in the sphincter of Oddi to reduce postoperative pancreatic fistula a... | |||||||||||||
| Medical condition: Elective distal pancreatectomy for any underlying disease | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2018-004139-66 | Sponsor Protocol Number: AGO/2018/006 | Start Date*: 2019-04-11 |
| Sponsor Name:Ghent University Hospital | ||
| Full Title: Effect of norepinephrine infusion on hepatic blood flow during goal-directed hemodynamic therapy. | ||
| Medical condition: hepatic blood flow hepatic vascular pressures | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: BE (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2015-003504-22 | Sponsor Protocol Number: UCDCRC/015/006 | Start Date*: 2015-10-09 | |||||||||||
| Sponsor Name:UCD | |||||||||||||
| Full Title: The NAPRESSIM trial. The use of low dose prophylactic naloxone infusion to prevent respiratory depression with intrathecal morphine. | |||||||||||||
| Medical condition: Respiratory Depression | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IE (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: 2016-001673-32 | Sponsor Protocol Number: P150915 | Start Date*: 2016-10-19 | |||||||||||
| Sponsor Name:ASSISTANCE PUBLIQUE - HOPITAUX DE PARIS (AP-HP) | |||||||||||||
| Full Title: PREVENTION OF POSTOPERATIVE PANCREATIC FISTULA BY SOMATOSTATIN (PREFIPS) | |||||||||||||
| Medical condition: Patients candidate for pancreatic surgery (pancreaticoduodenectomy or distal pancreatectomy with or without splenectomy). | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2016-000212-16 | Sponsor Protocol Number: HYKS-190116 | Start Date*: 2016-04-12 |
| Sponsor Name:Helsinki University Central Hospital | ||
| Full Title: Hydrocortisone vs. pasireotide in preventing pancreatic fistula and other complications after pancreatic resection - a prospective, randomized, controlled trial | ||
| Medical condition: Patients undergoing pancreatic resection. | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: FI (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2010-022640-20 | Sponsor Protocol Number: JL23 | Start Date*: 2011-01-12 | |||||||||||
| Sponsor Name:Johanna Laukkarinen | |||||||||||||
| Full Title: Cortisone treatment for the prevention of postoperative pancreatitis and pancreatitis-induced complications after pancreaticoduodenectomy (Whipple operation). | |||||||||||||
| Medical condition: Tutkittavat potilaat ovat leikkauspotilaita, joille suoritetaan rutiinisti haimanpään-ja pohjukaissuolen poistoleikkaus (Whipplen operaatio) joko kasvaimen tai kroonisen haimatulehduksen vuoksi. | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FI (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2008-004231-38 | Sponsor Protocol Number: 08-BO-VIBH | Start Date*: 2009-01-26 | |||||||||||
| Sponsor Name:Department of Medicine I, University Hospital St.Josef-Hospital, Ruhr University Bochum | |||||||||||||
| Full Title: Effects of vildagliptin (Galvus®) on beta-cell function and turnover in humans | |||||||||||||
| Medical condition: Diabetes mellitus, beta-cell function before and after pancreatic surgery | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2005-004854-29 | Sponsor Protocol Number: S245.4.008 | Start Date*: 2007-09-21 | |||||||||||
| Sponsor Name:Abbott Products GmbH | |||||||||||||
| Full Title: One week double-blind, randomized, placebo-controlled, parallel-group, multi-center study with Creon® 25000 Minimicrospheres™ in subjects with pancreatic exocrine insufficiency after pancreatic sur... | |||||||||||||
| Medical condition: Pancreatic Exocrine Insufficiency | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) IT (Completed) BG (Completed) HU (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2012-002638-35 | Sponsor Protocol Number: 3.00 | Start Date*: 2012-07-31 |
| Sponsor Name:Stockholms Läns Landsting, Karolinska Universitetssjukhuset Huddinge, Anestesikliniken | ||
| Full Title: ALBUMIN KINETICS BY 123I-HSA A validation study on healthy volunteers, patients with acute inflammation, and patiens scheduled for major abdominal surgery | ||
| Medical condition: A) healthy volunteers (transcapillary escape rate of albumin, plasmavolume, and turnover of albumin) B) Acute inflammation such as pancreatitis or cholecystitis C) Scheduled major abdominal surge... | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: SE (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2007-000375-42 | Sponsor Protocol Number: S339.2.001 | Start Date*: 2008-02-21 | |||||||||||
| Sponsor Name:Solvay Pharmaceuticals GmbH | |||||||||||||
| Full Title: A multi-center, double-blind, parallel-design, randomized, placebo-controlled, dose-ranging study to assess the efficacy and safety of oral recombinant microbial lipase (SLV339) in subjects with pa... | |||||||||||||
| Medical condition: Pancreatic exocrine insufficiency due to chronic pancreatitis | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: DK (Completed) SE (Prematurely Ended) HU (Prematurely Ended) CZ (Completed) LV (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2017-004547-21 | Sponsor Protocol Number: ZP4207-17109 | Start Date*: 2018-08-24 | |||||||||||
| Sponsor Name:Zealand Pharma A/S | |||||||||||||
| Full Title: A Two-Period, Open-label Trial Evaluating the Efficacy and Safety of Dasiglucagon for the Treatment of Children with Congenital Hyperinsulinism | |||||||||||||
| Medical condition: Children with congenital hyperinsulinism | |||||||||||||
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| Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (GB - no longer in EU/EEA) DE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2017-004546-15 | Sponsor Protocol Number: ZP4207-17106 | Start Date*: 2018-08-24 | |||||||||||
| Sponsor Name:Zealand Pharma A/S | |||||||||||||
| Full Title: An Extension Trial Evaluating the Long-term Safety and Efficacy of Dasiglucagon for the Treatment of Children with Congenital Hyperinsulinism | |||||||||||||
| Medical condition: Children with congenital hyperinsulinism | |||||||||||||
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| Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (GB - no longer in EU/EEA) DE (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2018-000415-25 | Sponsor Protocol Number: PROSPER | Start Date*: 2018-08-10 | |||||||||||
| Sponsor Name:University Hospital Heidelberg | |||||||||||||
| Full Title: PANCREATIC RESECTION WITH PERIOPERATIVE OFF-LABEL STUDY OF PROPRANOLOL AND ETODOLAC – A PHASE II RANDOMIZED TRIAL | |||||||||||||
| Medical condition: Patients with pancreatic carcinoma treated by pancreatoduodenectomy. | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2020-005483-66 | Sponsor Protocol Number: RASTA | Start Date*: 2021-11-18 | ||||||||||||||||
| Sponsor Name:UNIVERSITÀ DEGLI STUDI MILANO BICOCCA | ||||||||||||||||||
| Full Title: ERAS versus ERAS plus arTificiAl nutrition in open pancreatoduodenectomy (The RASTA trial) | ||||||||||||||||||
| Medical condition: Periampullary or pancreatic cancer | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: IT (Completed) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2010-021477-36 | Sponsor Protocol Number: NEOPAC | Start Date*: 2015-01-30 | ||||||||||||||||
| Sponsor Name:Gesellschaft für Studienmanagement und Onkologie mbH | ||||||||||||||||||
| Full Title: Adjuvant chemotherapy versus NEOadjuvant gemcitabine/ oxaliplatin plus adjuvant gemcitabine in resectable PAncreatic Cancer: a randomized multicenter phase III study | ||||||||||||||||||
| Medical condition: resectable pancreatic cancer | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: DE (Completed) BE (Completed) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2011-006174-47 | Sponsor Protocol Number: FC-004 | Start Date*: 2012-06-08 | |||||||||||
| Sponsor Name:ProFibrix BV | |||||||||||||
| Full Title: A Phase 3, Randomized, Single-Blind, Controlled Trial of Topical Fibrocaps™ in Intraoperative Surgical Haemostasis | |||||||||||||
| Medical condition: Intraoperative Surgical Hemostasis (Spinal Surgery, Vascular Surgery, Hepatic resection, Soft tissue dissection) | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: BE (Completed) NL (Completed) GB (Completed) | |||||||||||||
| Trial results: Removed from public view | |||||||||||||
| EudraCT Number: 2008-006981-27 | Sponsor Protocol Number: C14007 | Start Date*: 2011-01-13 | ||||||||||||||||||||||||||||||||||||
| Sponsor Name:Millennium Pharmaceuticals, Inc | ||||||||||||||||||||||||||||||||||||||
| Full Title: A Phase 1 Dose Escalation Study of MLN8237, an Aurora A Kinase Inhibitor, in Adult Patients With Nonhematological Malignancies, Followed by a Phase 2 of MLN8237 in Lung, Breast, Head and Neck, or G... | ||||||||||||||||||||||||||||||||||||||
| Medical condition: Phase I portion of the study - Advanced nonhematologic malignancies. Phase II portion of the study - Non-small cell lung cancer (NSCLC), small cell lung cancer (SCLC), adenocarcinoma of the esop... | ||||||||||||||||||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||
| Trial protocol: CZ (Completed) | ||||||||||||||||||||||||||||||||||||||
| Trial results: View results | ||||||||||||||||||||||||||||||||||||||
| EudraCT Number: 2017-004545-24 | Sponsor Protocol Number: ZP4207-17103 | Start Date*: 2018-12-29 | |||||||||||
| Sponsor Name:Zealand Pharma A/S | |||||||||||||
| Full Title: A Randomized Trial in 2 Parts: Double-Blind, Placebo-Controlled, Crossover Part 1 and Open-label Part 2, Evaluating the Efficacy and Safety of Dasiglucagon for the Treatment of Children with Congen... | |||||||||||||
| Medical condition: Children with congenital hyperinsulinism | |||||||||||||
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| Population Age: Newborns, Infants and toddlers, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) GB (GB - no longer in EU/EEA) | |||||||||||||
| Trial results: View results | |||||||||||||
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