- Trials with a EudraCT protocol (44,393)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
44,393 result(s) found.
Displaying page 1,526 of 2,220.
| EudraCT Number: 2009-015716-18 | Sponsor Protocol Number: AT08/09 | Start Date*: 2009-09-18 | |||||||||||
| Sponsor Name:University Hospitals Leuven | |||||||||||||
| Full Title: A comparative trial between the analgesic efficacy of a standard postoperative analgesic regimen and TAP- block in addition to a standard postoperative regimen after inguinal hernia repair in a su... | |||||||||||||
| Medical condition: Pain treatment after laparascopic ingiunal hernia repair. | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: BE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2018-002233-37 | Sponsor Protocol Number: IPX203-B16-02 | Start Date*: 2019-03-18 | |||||||||||||||||||||
| Sponsor Name:Impax Laboratories, LLC | |||||||||||||||||||||||
| Full Title: A randomized controlled study to compare the safety and efficacy of IPX203 with immediate-release carbidopa-levodopa in Parkinson's disease patients with motor fluctuations. | |||||||||||||||||||||||
| Medical condition: Parkinson's disease | |||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
| Trial protocol: CZ (Completed) DE (Completed) GB (GB - no longer in EU/EEA) PL (Completed) IT (Completed) | |||||||||||||||||||||||
| Trial results: View results | |||||||||||||||||||||||
| EudraCT Number: 2017-002468-41 | Sponsor Protocol Number: Dial-1 | Start Date*: 2018-06-21 | |||||||||||
| Sponsor Name:University Medical Center of the Johannes Gutenberg- University Mainz | |||||||||||||
| Full Title: A phase I/II multicenter, open-label Study of DKN-01 to investigate the anti-tumor activity and safety of DKN-01 in Patients with Hepatocellular Carcinoma and WNT signaling Alterations | |||||||||||||
| Medical condition: Hepatocellular Carcinoma | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2007-006125-28 | Sponsor Protocol Number: AT 15/10/07 | Start Date*: 2007-12-17 |
| Sponsor Name:University Hospitals Leuven | ||
| Full Title: Comparison of intrathecal low-dose ropivacaine, bupivacaine and lidocaine for knee arthroscopy in ambulatory setting. a randomised, double-blind trial; | ||
| Medical condition: Male and female patients, scheduled for an elective knee arthroscopy. | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: BE (Completed) | ||
| Trial results: View results | ||
| 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: 2017-000456-26 | Sponsor Protocol Number: Tumorspheres_Colrec | Start Date*: 2017-07-10 | |||||||||||
| Sponsor Name:Vejle Hospital | |||||||||||||
| Full Title: Predictive value of in-vitro testing anti-cancer therapy sensitivity on tumorspheres from patients with metastatic colorectal cancer | |||||||||||||
| Medical condition: | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DK (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2016-002956-25 | Sponsor Protocol Number: MAS-OLE-16-003 | Start Date*: 2016-11-18 | |||||||||||
| Sponsor Name:FONDAZIONE POLICLINICO UNIVERSITARIO AGOSTINO GEMELLI IRCCS UNIVERSITA' CATTOLICA DEL SACRO CUORE | |||||||||||||
| Full Title: Olevia for the prevention of atrial fibrillation post heart valve-surgery. | |||||||||||||
| Medical condition: POST-OPERATIVE ATRIAL FIBRILLATION | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2017-000589-31 | Sponsor Protocol Number: NEMESIS | Start Date*: 2018-02-02 | ||||||||||||||||
| Sponsor Name:SOCIETà CAMPANA DI IMMUNOTERAPIA ONCOLOGICA | ||||||||||||||||||
| Full Title: multi stage phase II trial of Nivolumab (an anti –PD-1) in patients with platinum resistant Mismatch Repair deficient germinal cells tumours | ||||||||||||||||||
| Medical condition: patients with platinum resistant Mismatch Repair deficient germinal cells tumours | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male | |||||||||||||||||
| Trial protocol: IT (Prematurely Ended) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2015-005090-20 | Sponsor Protocol Number: FADOI.01.2016 | Start Date*: 2018-05-17 | ||||||||||||||||
| Sponsor Name:FONDAZIONE FADOI | ||||||||||||||||||
| Full Title: Rivaroxaban or placebo for extended antithrombotic prophylaxis after laparoscopic surgery for colorectal cancer: a randomized, double blind, placebo-controlled study. THE PRO-LAPS STUDY II | ||||||||||||||||||
| Medical condition: Prevention of venous thromboembolism after laparoscopic surgery for colorectal cancer | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: IT (Prematurely Ended) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2018-003542-17 | Sponsor Protocol Number: FISM_IRON-MDS | Start Date*: 2019-05-06 | |||||||||||
| Sponsor Name:FONDAZIONE ITALIANA SINDROMI MIELODISPLASTICHE ETS | |||||||||||||
| Full Title: Early and low dose Deferasirox (3.5 mg/kg FCT) to suppress NTBI and LPI as early intervention to prevent tissue iron overload in lower risk MDS | |||||||||||||
| Medical condition: Adult patients with low risk MDS | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Prematurely Ended) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2018-001741-14 | Sponsor Protocol Number: TEM-MM-101 | Start Date*: 2018-12-13 | |||||||||||
| Sponsor Name:OSPEDALE SAN RAFFAELE | |||||||||||||
| Full Title: A phase I/II dose escalation study evaluating safety and activity of autologous CD34+-enriched hematopoietic progenitor cells genetically modified with a lentiviral vector encoding for the human in... | |||||||||||||
| Medical condition: Multiple myeloma in early relapse after intensive front line therapy | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2020-005343-23 | Sponsor Protocol Number: ADAIDO | Start Date*: 2021-05-28 | |||||||||||
| Sponsor Name:IRCCS ISTITUTO ORTOPEDICO GALEAZZI S.P.A | |||||||||||||
| Full Title: Effect of the antiresorptive treatment with alendronate versus no treatment after denosumab and aromatase inhibitors discontinuation in low fracture risk osteopenic postmenopausal women with non me... | |||||||||||||
| Medical condition: post-menopausal osteoporosis in women with non-metastatic hormonal receptor positive (HR+) breast cancer. | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Female | ||||||||||||
| Trial protocol: IT (Prematurely Ended) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2012-003729-62 | Sponsor Protocol Number: R-Verapamil-001 | Start Date*: 2013-01-16 | |||||||||||
| Sponsor Name:CENTER LABORATORIES, INC | |||||||||||||
| Full Title: A Randomized, Placebo-Controlled, Double-Blind, Parallel-Group, Phase 2 Study to Evaluate the Safety and Efficacy of R-Verapamil in the Prophylaxis of Episodic Cluster Headache | |||||||||||||
| Medical condition: Episodic Cluster Headache | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2020-002533-14 | Sponsor Protocol Number: REVERT | Start Date*: 2021-02-15 | ||||||||||||||||
| Sponsor Name:DIP. MEDICINA DEI SISTEMI UNIVERSITà DEGLI STUDI DI ROMA TOR VERGATA | ||||||||||||||||||
| Full Title: REVERT – taRgeted thErapy for adVanced colorEctal canceR paTients. | ||||||||||||||||||
| Medical condition: unresectable metastatic colorectal cancer (mCRC) | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: IT (Prematurely Ended) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2018-002948-88 | Sponsor Protocol Number: CRETA | Start Date*: 2019-02-20 | |||||||||||
| Sponsor Name:ALMA MATER STUDIORUM UNIVERSITà DI BOLOGNA | |||||||||||||
| Full Title: Phase II study to evaluate the activity and safety of Cabozantinib in pretreated, advanced RET-reArranged non-small cell lung cancer patients: CRETA trial | |||||||||||||
| Medical condition: Advanced RET-rearranged non-small cell lung cancer | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Prematurely Ended) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2015-001767-40 | Sponsor Protocol Number: AZALEA704 | Start Date*: 2016-11-10 | |||||||||||
| Sponsor Name:AZIENDA OSPEDALIERA "OSPEDALI RIUNITI MARCHE NORD" | |||||||||||||
| Full Title: A phase II study testing the efficacy of combined azacitidine and lenalidomide for non-M3 acute myeloid leukemia (AML) patients aged between 60 and 70 years, fit, relapsed or refractory: the AZALEA... | |||||||||||||
| Medical condition: ACUTE MYELOID LEUKEMIA | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Prematurely Ended) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2017-002340-32 | Sponsor Protocol Number: APIDULCIS | Start Date*: 2019-03-19 | ||||||||||||||||
| Sponsor Name:FONDAZIONE ARIANNA ANTICOAGULAZIONE | ||||||||||||||||||
| Full Title: APIDULCIS: Extended anticoagulation with low-dose apixaban after a standard course anticoagulation in patients with a first venous thromboembolism who have positive d-dimer | ||||||||||||||||||
| Medical condition: a first episode of proximal deep vein thrombosis (DVT) and/or pulmonary embolism (PE) | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: IT (Prematurely Ended) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2015-001868-19 | Sponsor Protocol Number: 2015-001 | Start Date*: 2015-10-15 | |||||||||||
| Sponsor Name:University medical center of Johannes Gutenberg University Mainz | |||||||||||||
| Full Title: A randomized, double-blind, placebo-controlled, mono-center study to evaluate the effects of mepolizumab on airway physiology in patients with eosinophilic asthma: the MEMORY study | |||||||||||||
| Medical condition: severe eosinophilic asthma | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2016-000284-17 | Sponsor Protocol Number: VinoMetro2015-007 | Start Date*: 2016-11-11 |
| Sponsor Name:Universitätsmedizin Mainz | ||
| Full Title: Phase II study of metronomic treatment with daily oral vinorelbine as first-line chemotherapy in patients with advanced/metastatic HR+/HER2- breast cancer resistant to endocrine therapy (VinoMetro). | ||
| Medical condition: HR+/HER2- advanced/metastatic breast cancer | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Female | |
| Trial protocol: DE (Prematurely Ended) | ||
| Trial results: View results | ||
| EudraCT Number: 2013-005364-26 | Sponsor Protocol Number: RE-LATED-AF | Start Date*: 2014-07-17 |
| Sponsor Name:University Medical Center of the Johannes Gutenberg University Mainz | ||
| Full Title: Resolution of Left Atrial-Appendage Thrombus – Effects of Dabigatran in patients with AF (RE-LATED AF) – A Prospective, multicenter, randomized, open-label, controlled, explorative, blinded-endpoin... | ||
| Medical condition: Left atrial-appendage thrombus in atrial fibrillation | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: DE (Prematurely Ended) | ||
| Trial results: View results | ||
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