- Trials with a EudraCT protocol (19)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
19 result(s) found for: Bleeding diathesis.
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EudraCT Number: 2005-005918-20 | Sponsor Protocol Number: ITP001 | Start Date*: 2008-12-23 | |||||||||||
Sponsor Name:Rikshospitalet | |||||||||||||
Full Title: Rituximab as second line treatment for ITP: A Multicentre, Randomized, Double blind, Placebo-controlled, Phase III study. “The RITP study” | |||||||||||||
Medical condition: Immune thrombocytopenic purpura (ITP) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) SE (Completed) GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-005174-23 | Sponsor Protocol Number: CAVA2Dec04 | Start Date*: 2005-04-11 |
Sponsor Name:NHS Grampian | ||
Full Title: Is smooth muscle mitogenesis down regulated by platelet inactivation with combination antiplatelet therapy after angioplasty for claudication? | ||
Medical condition: Intermittent claudication = stenosis of superficial femoral artery requiring percutaneous angioplasty | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2007-003635-23 | Sponsor Protocol Number: XIG-AP 1 | Start Date*: 2008-08-14 | |||||||||||
Sponsor Name:Central Manchester and Manchester Children's Hospitals NHS Trust | |||||||||||||
Full Title: A PRELIMINARY EVALUATION OF THE SAFETY PROFILE OF TWENTY-FOUR HOUR INFUSION OF HUMAN RECOMBINANT ACTIVATED PROTEIN C (XIGRIS) EARLY IN SEVERE ACUTE PANCREATITIS. | |||||||||||||
Medical condition: Severe acute pancreatitis in man (with an APACHE II score of ≥ 15) appears to carry a considerably higher risk of death when compared to general critical care patients with similar APACHE II scores... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-002794-11 | Sponsor Protocol Number: NL49960.018.14 | Start Date*: 2014-12-08 |
Sponsor Name:Academic Medical Center | ||
Full Title: Adjuvant hyperthermic intraperitoneal chemotherapy in patients with colon cancer at high risk of peritoneal carcinomatosis; the COLOPEC randomized multicenter trial | ||
Medical condition: Adjuvant hyperthermic intraperitoneal chemotherapy in patients with colon cancer at high risk of peritoneal carcinomatosis; the COLOPEC randomized multicenter trial | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2008-006371-67 | Sponsor Protocol Number: RLBUHT 3729 | Start Date*: 2009-09-10 |
Sponsor Name:Royal Liverpool and Broadgreen University Hospital [...] | ||
Full Title: EFFECT OF THIENOPYRIDINE DERIVATIVE (CLOPIDOGREL) ON THE DISPOSITION OF EFAVIRENZ AND NEVIRAPINE IN HIV POSITIVE PATIENTS | ||
Medical condition: To determine whether anti-platelet agent clopidigrel influences the disposition of NNRTIs (efavirenz and nevirapine) | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: GB (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2016-002885-30 | Sponsor Protocol Number: ARES | Start Date*: 2017-07-27 | |||||||||||
Sponsor Name:FONDAZIONE POLICLINICO UNIVERSITARIO AGOSTINO GEMELLI IRCCS UNIVERSITA' CATTOLICA DEL SACRO CUORE | |||||||||||||
Full Title: Novel strategies of antithrombotic prophylaxis in patients with Essential Thrombocythemia (ET) at high risk of cardiovascular events: comparison of different dosing regimens of administration of l... | |||||||||||||
Medical condition: Essential thrombocytemia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-001341-14 | Sponsor Protocol Number: BAY 59-7939 / 11527 | Start Date*: 2004-11-04 | |||||||||||
Sponsor Name:Bayer HealthCare AG | |||||||||||||
Full Title: Controlled, Double-Blind, Randomized, Dose-ranging Study of once-daily regimen of BAY59-7939 in the Prevention of VTE in Patients Undergoing Elective Total Hip Replacement-ODIXaHIP-OD Study | |||||||||||||
Medical condition: Deep Venous Thrombosis prophylaxis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) SE (Completed) AT (Completed) ES (Completed) GB (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-011899-30 | Sponsor Protocol Number: 20080259 | Start Date*: 2009-12-18 | |||||||||||
Sponsor Name:Amgen Inc | |||||||||||||
Full Title: A Phase 3, Randomized, Double-blind, Placebo-controlled Study of Pegfilgrastim Administered to Subjects With Newly Diagnosed, Locally-advanced or Metastatic Colorectal Cancer Treated With Bevacizum... | |||||||||||||
Medical condition: Locally-advanced or Metastatic Colorectal Cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: LV (Completed) HU (Completed) CZ (Completed) BE (Completed) IE (Completed) IT (Completed) FR (Completed) SK (Completed) BG (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-005217-22 | Sponsor Protocol Number: RD.03.SPR.29079 | Start Date*: 2009-03-04 | |||||||||||
Sponsor Name:Galderma Research & Development | |||||||||||||
Full Title: Efficacy and Safety of Clobetasol propionate shampoo 0.05% used in association with an antifungal shampoo in the treatment of moderate to severe Scalp Seborrheic Dermatitis | |||||||||||||
Medical condition: moderate to severe Scalp Seborrheic Dermatitis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-000941-12 | Sponsor Protocol Number: BAY 43-9006 / 11718 | Start Date*: 2005-08-18 |
Sponsor Name:Onyx Pharmaceuticals, Inc. | ||
Full Title: Phase III randomised, placebo controlled study of sorafenib in repeated cycles of 21 days in combination with paclitaxel/carboplatin chemotherapy in subjects with unresectable stage III or stage IV... | ||
Medical condition: unresectable, advanced Stage III or Stage IV melanoma | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2007-002828-15 | Sponsor Protocol Number: S 379 | Start Date*: 2009-03-13 |
Sponsor Name:Krankenhaus Nordwest GmbH | ||
Full Title: An open-label, uncontrolled phase II trial of single agent sunitinib (SU 11248) for patients with chemo-refractory metastatic melanoma | ||
Medical condition: chemo-refractory metastatic melanoma | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2019-001896-35 | Sponsor Protocol Number: PUMA-NER-6203 | Start Date*: 2020-01-30 | |||||||||||||||||||||||||||||||
Sponsor Name:Puma Biotechnology, Inc | |||||||||||||||||||||||||||||||||
Full Title: An Open-Label Phase 2 Study to Characterize Colon Pathology in Patients With HER2 Amplified Breast Cancer Treated With Neratinib | |||||||||||||||||||||||||||||||||
Medical condition: HER2 amplified (HER2+) stage 1 through stage 4 primary adenocarcinoma of the breast | |||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||
Trial protocol: PT (Completed) | |||||||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2018-002947-27 | Sponsor Protocol Number: SIMCODE | Start Date*: 2020-01-22 |
Sponsor Name:Charité – Universitätsmedizin Berlin | ||
Full Title: Simvastatin add-on to Escitalopram in patients with comorbid obesity and major depression: A multicenter, randomized, double-blind, placebo-controlled trial | ||
Medical condition: Patients with comorbid obesity (body mass index ≥ 30) and major depression | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2014-004619-36 | Sponsor Protocol Number: TS-102 | Start Date*: 2015-03-11 | ||||||||||||||||
Sponsor Name:Biocompatibles UK Ltd. | ||||||||||||||||||
Full Title: A Phase III Clinical Trial Evaluating TheraSphere® in Patients with Metastatic Colorectal Carcinoma of the Liver who have Failed First Line Chemotherapy | ||||||||||||||||||
Medical condition: Metastatic Colorectal Carcinoma of the Liver | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: BE (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2004-004061-15 | Sponsor Protocol Number: SPD422-403 | Start Date*: 2005-07-07 | |||||||||||
Sponsor Name:Shire Pharmaceutical Development Ltd. | |||||||||||||
Full Title: A Phase IIIb, randomised, open label study to compare the safety, efficacy and tolerability of anagrelide hydrochloride versus hydroxyurea in high-risk essential thrombocythaemia patients. | |||||||||||||
Medical condition: Essential thrombocythaemia (ET) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) IE (Completed) ES (Completed) IT (Completed) SK (Completed) CZ (Completed) SI (Completed) BG (Completed) PL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-005792-12 | Sponsor Protocol Number: GOIRC-06-2020 | Start Date*: 2022-04-05 | |||||||||||
Sponsor Name:GRUPPO ONCOLOGICO ITALIANO DI RICERCA CLINICA (GOIRC) | |||||||||||||
Full Title: Pilot ‘Window of Opportunity’ Neoadjuvant Study of Abemaciclib in Low-Estrogen Receptor (ER) positive/Human Epidermal Growth Factor Receptor 2 (HER2)-negative Early Breast Cancer (BC) | |||||||||||||
Medical condition: Low-Estrogen Receptor (ER) positive/Human Epidermal Growth Factor Receptor 2 (HER2)-negative Early Breast Cancer (BC) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-003659-13 | Sponsor Protocol Number: IMG-7289-CTP-201 | Start Date*: 2020-06-21 | |||||||||||
Sponsor Name:Imago BioSciences Inc. | |||||||||||||
Full Title: A Phase 2 Multi-Center, Open Label Study to Assess the Safety,Efficacy and Pharmacodynamics of IMG-7289 in Patients with Essential Thrombocythemia | |||||||||||||
Medical condition: Patients with essential thrombocythemia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) GB (GB - no longer in EU/EEA) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-007974-39 | Sponsor Protocol Number: AIO-KRK-0207 | Start Date*: 2009-08-04 | ||||||||||||||||
Sponsor Name:AIO-Studien-gGmbH | ||||||||||||||||||
Full Title: Randomized three arm phase III trial on induction treatment with a fluoropyrimidine-, oxaliplatin- and bevacizumab-based chemotherapy for 24 weeks followed by maintenance treatment with a fluoropyr... | ||||||||||||||||||
Medical condition: Histologically confirmed and inoperable or irresectable metastatic colorectal cancer (stage IV) | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2012-005375-14 | Sponsor Protocol Number: TS-104 | Start Date*: 2013-06-03 | ||||||||||||||||
Sponsor Name:Biocompatibles UK Ltd | ||||||||||||||||||
Full Title: A prospective randomized clinical trial on 90Yttrium trans-arterial radio-Embolization (Therasphere) vs. standard of care (sorafenib) for the treatment of advanced Hepatocellular carcinoma (HCC) ... | ||||||||||||||||||
Medical condition: Advanced Hepatocellular Carcinoma (HCC) with Portal Vein Thrombosis (PVT) | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: BE (Completed) GB (Prematurely Ended) ES (Prematurely Ended) | ||||||||||||||||||
Trial results: View results |
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