- Trials with a EudraCT protocol (74)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
74 result(s) found for: conventional resection.
Displaying page 1 of 4.
EudraCT Number: 2010-018480-42 | Sponsor Protocol Number: 550904 | Start Date*: 2010-11-12 | ||||||||||||||||
Sponsor Name:Baxter Innovations GmbH | ||||||||||||||||||
Full Title: A RANDOMIZED, CONTROLLED, MULTICENTER PHASE 2 STUDY TO EVALUATE THE EFFICACY AND SAFETY OF FIBRIN SEALANT VH S/D 500 S-APR (TISSEEL) FOR HEMOSTASIS IN SUBJECTS UNDERGOING HEPATIC RESECTION | ||||||||||||||||||
Medical condition: Hemostasis in hepatic resection | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Completed) | ||||||||||||||||||
Trial results: View results |
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: 2017-004070-34 | Sponsor Protocol Number: PRECAVE | Start Date*: 2018-01-29 |
Sponsor Name:Servicio de Urología. Hospital Universitario La Paz | ||
Full Title: RANDOMIZED CLINICAL TRIAL, OPEN, TO EVALUATE THE BLADDER INSTILLATION OF NEOADYUVANT CHEMOTHERAPY TO THE TRANSURETHAL RESECTION OF BLADDER FOR THE PREVENTION OF RECURRENCE OF NONMUSCLE-INVASIVE URO... | ||
Medical condition: Non-muscle-invasive urothelial carcinoma | ||
Disease: | ||
Population Age: Elderly | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2013-001725-10 | Sponsor Protocol Number: 13-001 | Start Date*: 2014-01-24 |
Sponsor Name:Medizinische Universität Wien | ||
Full Title: Bronchoscopic indocyanine green fluorescence imaging for the evaluation of tracheal perfusion after surgery | ||
Medical condition: Tracheal stenosis secondary to malign and benign conditions | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Completed) | ||
Trial results: View results |
EudraCT Number: 2006-001785-16 | Sponsor Protocol Number: 2006/3:1 | Start Date*: 2006-06-15 |
Sponsor Name:Karolinska universitetssjukhuset | ||
Full Title: Neo-adjuvant behandling av esofagus-cardia cancer inför kurativt syftande resektion. Jämförande studie mellan kemo- och radiokemobehandling. | ||
Medical condition: Cancer of the esophagus or gastricardia concidered to be resectable at the preoperative evaluation. The following TN stages will be enrolled: T1-3, N1, T2-3N0 and T2-3N1. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: SE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2016-001493-15 | Sponsor Protocol Number: UC-0110/1610 | Start Date*: 2017-10-13 |
Sponsor Name:UNICANCER | ||
Full Title: A randomized phase II study comparing treatment intensification with hepatic arterial infusion chemotherapy plus systemic chemotherapy to systemic chemotherapy alone in patients with liver-only col... | ||
Medical condition: Patients with liver-only non resectable colorectal metastases. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FR (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2019-004512-58 | Sponsor Protocol Number: INV-GEM-0200-I | Start Date*: 2020-08-17 | |||||||||||
Sponsor Name:Technische Universität München, Fakultät für Medizin | |||||||||||||
Full Title: Comparison of Fluorescein-INtra-VItal microscopy Versus conventional frozen section diagnosis for intraOperative histopathological evaluation | |||||||||||||
Medical condition: Intracranial tumor | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-004250-17 | Sponsor Protocol Number: RG_18-205,BN3010 | Start Date*: 2019-10-11 | |||||||||||
Sponsor Name:University of Birmingham | |||||||||||||
Full Title: An International Prospective Trial on High-Risk Medulloblastoma in Patients Older than 3 Years | |||||||||||||
Medical condition: Histologically proven high-risk medulloblastoma, with any of the currently defined histological subtypes. High-risk disease is defined as patients with sonic hedgehog (SHH) subgroup or non-SHH/non-... | |||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) AT (Trial now transitioned) DK (Trial now transitioned) IT (Trial now transitioned) NO (Trial now transitioned) NL (Trial now transitioned) BE (Trial now transitioned) SE (Trial now transitioned) CZ (Trial now transitioned) DE (Trial now transitioned) FI (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-003930-17 | Sponsor Protocol Number: 1407-GUCG | Start Date*: 2015-10-05 | |||||||||||
Sponsor Name:European Organisation for Research and Treatment of Cancer (EORTC) | |||||||||||||
Full Title: A RANDOMIZED PHASE III TRIAL COMPARING CONVENTIONAL-DOSE CHEMOTHERAPY USING PACLITAXEL, IFOSFAMIDE, AND CISPLATIN (TIP) WITH HIGH-DOSE CHEMOTHERAPY USING MOBILIZING PACLITAXEL PLUS IFOSFAMIDE FOLLO... | |||||||||||||
Medical condition: progressive or recurrent germ cell tumor (measurable or non-measurable) | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: BE (Trial now transitioned) DK (Trial now transitioned) IE (Trial now transitioned) FR (Trial now transitioned) NL (Trial now transitioned) SI (Completed) ES (Ongoing) DE (Trial now transitioned) IT (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-001802-25 | Sponsor Protocol Number: 28-03-2007 | Start Date*: 2008-10-27 | |||||||||||
Sponsor Name:Johann-Wolfgang Goethe-Universität | |||||||||||||
Full Title: An exploratory, open label phase II study to evaluate the feasibility of contrast-enhanced MRI for measurement of perfusion in squamous cell cancer of the head & neck: comparison of the intravascul... | |||||||||||||
Medical condition: Patients of both gender are eligible for this study in case they present with the diagnosis of a primary squamous cell carcinoma of the head & neck after Magnevist-enhanced MRI, are scheduled for t... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-018447-34 | Sponsor Protocol Number: 06MH34 | Start Date*: 2011-09-22 | |||||||||||
Sponsor Name:Great Ormond Street Hospital for Children NHS Trust | |||||||||||||
Full Title: Investigation of dendritic cell vaccine immunotherapy in paediatric high grade glioma | |||||||||||||
Medical condition: Paediatric High grade glioma, excluding brain stem gliomas | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
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: 2005-000427-42 | Sponsor Protocol Number: LT 2005 XX | Start Date*: 2005-04-15 |
Sponsor Name:UK Children’s Cancer Study Group | ||
Full Title: SIOPEL 5 (HCC-1) trial on the hepatocellular carcinoma family of tumours in children/adolescents and young adults | ||
Medical condition: Hepatocellular carcinoma | ||
Disease: | ||
Population Age: Infants and toddlers, Children, Adolescents, Under 18, Adults | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2019-002729-31 | Sponsor Protocol Number: PETCOLINA1-FINBA | Start Date*: 2020-03-02 | |||||||||||
Sponsor Name:Fundación para la Investigación y la Innovación Biosanitaria del Principado de Asturias (FINBA) | |||||||||||||
Full Title: 18F-fluorocholine PET/CT in primary hyperparathyroidism with negative preoperative localization | |||||||||||||
Medical condition: Primary hyperthyroidism | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-005595-28 | Sponsor Protocol Number: AIO-TRK-0214 | Start Date*: 2015-09-29 | |||||||||||
Sponsor Name:AIO-Studien-gGmbH | |||||||||||||
Full Title: Induction therapy with gefitinib followed by taxane platinum chemotherapy and intercalated gefitinib in NSCLC stages II-IIIB with activating EGFR mutation – A single arm Phase II trial. | |||||||||||||
Medical condition: Patients with stage II, IIIA and IIIB non-squamous non-small-cell lung cancer with activating EGFR mutation | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-001200-20 | Sponsor Protocol Number: CSET 1287 | Start Date*: 2007-06-01 |
Sponsor Name:Institut Gustave Roussy | ||
Full Title: A Multicenter, Randomized Phase II Trial Assessing the Activity of Gemcitabine – Oxaliplatin Chemotherapy Alone or in Combination with Cetuximab in Patients with Advanced Biliary Cancer | ||
Medical condition: adenocarcinoma of the biliary tract ( gallbladder, intra and/ or extrahepatic bile ducts, ampulla of Vater) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FR (Ongoing) DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2008-000974-18 | Sponsor Protocol Number: AB07012 | Start Date*: 2009-05-06 | |||||||||||
Sponsor Name:AB SCIENCE | |||||||||||||
Full Title: A prospective, multicenter, randomized, double-blind, placebo-controlled, 2-parallel group, Phase III study to compare efficacy and safety of masitinib at 9 mg/kg/day in combination with gemcitabin... | |||||||||||||
Medical condition: advanced/metastatic pancreatic cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Completed) HU (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-001337-13 | Sponsor Protocol Number: CRAD001LIC34T | Start Date*: 2012-08-17 | |||||||||||
Sponsor Name:APRO | |||||||||||||
Full Title: A randomized phase II study to explore the efficacy and feasibility of upfront rotations between sunitinib and everolimus versus sequential treatment of first line sunitinib and second line everoli... | |||||||||||||
Medical condition: Metastatic clear cell renal cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) GR (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-002635-35 | Sponsor Protocol Number: Ph2_INBRX-109_SA_CS | Start Date*: 2022-02-11 | |||||||||||
Sponsor Name:Inhibrx, Inc. | |||||||||||||
Full Title: A Randomized, Blinded, Placebo-controlled, Phase 2 Study of INBRX-109 in Unresectable or Metastatic Conventional Chondrosarcoma | |||||||||||||
Medical condition: Unresectable or metastatic conventional chondrosarcoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Trial now transitioned) ES (Restarted) IT (Trial now transitioned) IE (Trial now transitioned) NL (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2004-002760-16 | Sponsor Protocol Number: 04/QO603/42 HEXVIX | Start Date*: 2005-01-12 | |||||||||||
Sponsor Name:Guy's and St Thomas' NHS Foundation Trust | |||||||||||||
Full Title: A randomised Study of “bluelight” hexyl amino levulinic acid (HAL) photodynamic assisted resection of bladder tumours versus conventional “white light” transurethral resection of newly diagnosed bl... | |||||||||||||
Medical condition: Superficial Bladder Cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
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