- Trials with a EudraCT protocol (49)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
49 result(s) found for: Gall bladder.
Displaying page 1 of 3.
EudraCT Number: 2007-000271-42 | Sponsor Protocol Number: 11012007 | Start Date*: 2007-05-08 | |||||||||||
Sponsor Name:Matti Eskelinen | |||||||||||||
Full Title: OKSIKODONIN ANALGEETTINEN PITOISUUS PLASMASSA YHDESSÄ PARASETAMOLIN 1g TAI 2g IV KANSSA ANNETTUNA MAHAKIRURGISILLA POTILAILLA | |||||||||||||
Medical condition: Tutkimukseen otetaan 24 sappileikkaukseen tulevaa perustervettä aikuispotilasta. | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2004-004316-23 | Sponsor Protocol Number: CLOMG | Start Date*: 2004-11-12 | |||||||||||
Sponsor Name:OSPEDALE S. RAFFAELE | |||||||||||||
Full Title: Randomised, controlled , double blind trial on emodinamic, analgesic, pharmacoeconomic effects of clonidine and magnesium in premedication of laparoscopic surgery for colecitis ablation. | |||||||||||||
Medical condition: Post operative analgesia. | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-004981-14 | Sponsor Protocol Number: OOI/KEMB/2006-2 | Start Date*: 2006-12-20 |
Sponsor Name:National Institute of Oncology, Budapest, Hungary | ||
Full Title: Phase II., non randomized, open study: inoperable gall bladder or biliary tract EGFR expressing carcinoma treatment with Erbitux and 5-fluorouracil, epiadriamycin, mitomycin containing combination ... | ||
Medical condition: Irresectable biliary tract cancer where palliation is the aim. It could be locally extanded and also metastatic cancer | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: HU (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2010-018850-11 | Sponsor Protocol Number: MHH_CCA_AG54 | Start Date*: 2011-04-15 | ||||||||||||||||
Sponsor Name:Medizinische Hochschule Hannover (MHH) | ||||||||||||||||||
Full Title: Panitumumab in combination with cisplatin/gemcitabine chemotherapy in patients with cholangiocarcinomas - a randomized clinical phase II study - PiCCA Study | ||||||||||||||||||
Medical condition: cholangiocarcinoma / gall bladder carcinoma | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Female | |||||||||||||||||
Trial protocol: DE (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2016-000084-16 | Sponsor Protocol Number: NC-6004-004A | Start Date*: 2016-11-24 | |||||||||||||||||||||
Sponsor Name:NanoCarrier Co, Ltd | |||||||||||||||||||||||
Full Title: A Phase 1b/2 Dose Escalation and Expansion Trial of NC-6004 (Nanoparticle Cisplatin) plus Gemcitabine in Patients with Advanced Solid Tumors or Squamous Non-Small Cell Lung, Biliary Tract, and Blad... | |||||||||||||||||||||||
Medical condition: Advanced solid tumors and first-line metastatic squamous NSCLC; first-line metastatic or locally advanced cholangiocarcinoma, gallbladder cancer, or ampullary cancer (biliary tract cancer); and fir... | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: BG (Completed) PL (Completed) IT (Completed) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-005135-15 | Sponsor Protocol Number: 8101 colloidAug08 | Start Date*: 2009-01-12 | ||||||||||||||||||||||||||||||||||||||||||||||
Sponsor Name:University of Nottingham | ||||||||||||||||||||||||||||||||||||||||||||||||
Full Title: Do 100 kiloDaltons matter? A prospective randomised double-blind study on the blood volume expanding effects of two different colloids in patients undergoing laparoscopic cholecystectomy | ||||||||||||||||||||||||||||||||||||||||||||||||
Medical condition: Patients undergoing laparoscopic cholecystectomy | ||||||||||||||||||||||||||||||||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||||||||||||
Trial protocol: GB (Completed) | ||||||||||||||||||||||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2017-001538-25 | Sponsor Protocol Number: AIO-HEP-0117 | Start Date*: 2018-03-12 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Sponsor Name:AIO-Studien-gGmbH | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Full Title: A randomized phase II trial of durvalumab and tremelimumab with gemcitabine or gemcitabine and cisplatin compared to gemcitabine and cisplatin in treatment-naïve patients with cholangio- and gallbl... | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Medical condition: advanced, unresectable and/or metastatic cholangio- and gallbladder carcinoma | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial protocol: DE (Completed) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-001308-35 | Sponsor Protocol Number: EB-UGI 01 | Start Date*: 2006-05-04 |
Sponsor Name:The Finsen Center, Rigshospitalet | ||
Full Title: A phase II study of erlotinib and bevacizumab in patients with advanced upper gastrointestinal carcinomas, refractory or intolerable to standard systemic therapy | ||
Medical condition: Histologically or cytologically verified upper gastro-intestinal carcinoma, including carcinomas of the esophagus, cardia, stomac, pancreas, gall bladder, and bile ducts of the following histologic... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DK (Completed) | ||
Trial results: View results |
EudraCT Number: 2006-001378-26 | Sponsor Protocol Number: 40776ORII/05IA01 | Start Date*: 2006-09-26 | |||||||||||
Sponsor Name:Laboratorios SALVAT, S.A. | |||||||||||||
Full Title: A Multicentre, Placebo Controlled, Randomised, Double-blind, Dose Ranging Study of SVT-40776 0.05 mg, 0.1 mg, 0.2 mg, Tolterodine 4 mg and Placebo Daily Doses for 4 Weeks in Patients Suffering from... | |||||||||||||
Medical condition: Overactive bladder (OAB) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) NL (Completed) CZ (Completed) HU (Completed) ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-004878-29 | Sponsor Protocol Number: NA | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:St. Antonius Hospital | |||||||||||||
Full Title: Perioperative antibiotic use in the treatment of acute calculous cholecystitis | |||||||||||||
Medical condition: Acute calculous cholecystitis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-001593-18 | Sponsor Protocol Number: 958 | Start Date*: 2015-06-02 |
Sponsor Name:Medizinische Universiät Wien | ||
Full Title: A pilot study to assess the influence of drug transporters on brain and organ distribution of erlotinib in humans | ||
Medical condition: Investigation in volunteers only | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2012-001705-24 | Sponsor Protocol Number: HE37/12 | Start Date*: 2013-02-20 | |||||||||||||||||||||
Sponsor Name:Hellenic Cooperative Oncology Group | |||||||||||||||||||||||
Full Title: Phase II single-arm study of first line treatment with gemcitabine and pazopanib in patients with inoperable locally advanced or metastatic biliary tree cancer (cholangiocarcinoma or gallbladder ca... | |||||||||||||||||||||||
Medical condition: Inoperable locally advanced or metastatic cancer of the biliary tree (cholangiocarcinoma and gallbladder carcinoma) | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: GR (Prematurely Ended) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2016-004692-53 | Sponsor Protocol Number: SJ-434 | Start Date*: 2017-03-01 | ||||||||||||||||||||||||||
Sponsor Name:Zealand University Hospital Køge | ||||||||||||||||||||||||||||
Full Title: Changes in bile acid homeostasis and stool habits after cholecystectomy | ||||||||||||||||||||||||||||
Medical condition: Post cholecystectomy bile acid diarrhoea/malabsorption | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: DK (Completed) | ||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2021-000179-36 | Sponsor Protocol Number: MS200647_0054 | Start Date*: 2021-10-15 | ||||||||||||||||||||||||||||||||||||
Sponsor Name:Merck KGaA | ||||||||||||||||||||||||||||||||||||||
Full Title: An Open-label, Multicenter Follow-up Study to Collect Long-term Data on Participants from Multiple Bintrafusp alfa (M7824) Clinical Studies | ||||||||||||||||||||||||||||||||||||||
Medical condition: Non-small cell lung cancer (NSCLC), biliary tract cancer (BTC), cervical cancer, and triple-negative breast cancer (TNBC) | ||||||||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||
Trial protocol: FR (Ongoing) BE (Completed) ES (Ongoing) IT (Completed) DE (Completed) | ||||||||||||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2022-000222-24 | Sponsor Protocol Number: CYC140-101 | Start Date*: 2022-06-07 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Sponsor Name:Cyclacel Pharmaceuticals | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Full Title: A PHASE 1/2, OPEN-LABEL, MULTICENTER STUDY TO INVESTIGATE THE SAFETY, PHARMACOKINETICS AND EFFICACY OF CYC140, AN ORAL PLK1 INHIBITOR, IN SUBJECTS WITH ADVANCED SOLID TUMORS AND LYMPHOMA | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Medical condition: ADVANCED SOLID TUMORS AND LYMPHOMA | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial protocol: ES (Ongoing) | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-000816-32 | Sponsor Protocol Number: FC-005 | Start Date*: 2014-10-17 | |||||||||||
Sponsor Name:ProFibrix, A wholly owned subsidary of the Medicines Company | |||||||||||||
Full Title: A Phase 3b, Randomized, Single-Blind, Controlled, Comparative Efficacy and Safety Study of Topical Fibrocaps™ (Raplixa™) and Tachosil® in Surgical Hemostasis during Hepatic Resection | |||||||||||||
Medical condition: Hepatic surgery specifically, hepatic wedge resection or anatomic resection of 1 to 5 contiguous hepatic segments, and/or other hepatic surgery, any of which may be combined with other surgical pro... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) AT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-005078-70 | Sponsor Protocol Number: ACTICCA-1 | Start Date*: 2014-01-16 | ||||||||||||||||
Sponsor Name:University Medical Center Hamburg-Eppendorf | ||||||||||||||||||
Full Title: Adjuvant chemotherapy with gemcitabine and cisplatin compared to standard of care after curative intent resection of cholangiocarcinoma and muscle invasive gallbladder carcinoma (ACTICCA-1 trial) ... | ||||||||||||||||||
Medical condition: Cholangiocarcinoma and gallbladder carcinoma | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Trial now transitioned) NL (Trial now transitioned) GB (GB - no longer in EU/EEA) DK (Completed) AT (Trial now transitioned) IT (Trial now transitioned) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-004867-19 | Sponsor Protocol Number: v1330032015 | Start Date*: 2015-02-24 |
Sponsor Name:Clinic for General Anesthesiology, Intensive Care and Pain Management | ||
Full Title: Perioperative fluid management in patients receiving major abdominal surgery – Effects of normal saline versus an acetate buffered balanced infusion solution on the necessity of catecholamines for ... | ||
Medical condition: hemodynamic stability of patients undergoing major surgery | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: AT (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2010-021240-18 | Sponsor Protocol Number: ARHSG062010 | Start Date*: 2011-04-19 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA S. GERARDO DI MONZA | |||||||||||||
Full Title: Peritoneal nebulization of Ropivacaine for pain control after laparoscopic colectomy | |||||||||||||
Medical condition: Elective Laparoscopic colectomy | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-004981-52 | Sponsor Protocol Number: GEMNABCCC-001 | Start Date*: 2016-09-28 | |||||||||||
Sponsor Name:University Hospital Essen | |||||||||||||
Full Title: Nab-Paclitaxel (Abraxane®) and Gemcitabine as first line therapy in patients with cholangiocarcinoma ineligible for cisplatin-based chemotherapy – a pilot study The NACHO trial (GEMNABCCC-001) | |||||||||||||
Medical condition: unresecable, metastatic or recurrent cholangiocarcinoma (intrahepatic cholangiocellular carcinoma, bile duct cancer, gall bladder carcinoma) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
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