- Trials with a EudraCT protocol (18)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (6)
18 result(s) found for: Splanchnic.
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EudraCT Number: 2017-000071-90 | Sponsor Protocol Number: AGO/2017/002 | Start Date*: 2017-03-15 |
Sponsor Name:Ghent University Hospital | ||
Full Title: Effect of sevoflurane and propofol on hepato-splanchnic pressure and flow during hepatobiliary surgery. | ||
Medical condition: patients scheduled for hepato-biliary surgery. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: View results |
EudraCT Number: 2012-002253-30 | Sponsor Protocol Number: SVT-RUXO#2012 | Start Date*: 2012-10-04 | |||||||||||
Sponsor Name:UNIVERSITA' DEGLI STUDI DI FIRENZE | |||||||||||||
Full Title: A phase 2 study of Ruxolitinib in patients with splanchnic vein thrombosis associated with myeloproliferative neoplasm | |||||||||||||
Medical condition: splanchnic vein thrombosis associated with myeloproliferative neoplasm | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-002036-14 | Sponsor Protocol Number: V3.10.5.2014 | Start Date*: 2014-08-08 | |||||||||||
Sponsor Name:Lars Bo Svendsen | |||||||||||||
Full Title: The effect of epidural anaesthesia on systemic and splanchnic hemodynamic during gastroesophageal resections, a randomized controlled trial | |||||||||||||
Medical condition: The effect of epidural anaesthesia on systemic and splanchnic hemodynamic during gastroesophageal cancer resection | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-004384-29 | Sponsor Protocol Number: Levosepsis1 | Start Date*: 2005-05-23 |
Sponsor Name:Dr GED DEMPSEY, University Hospital Aintree | ||
Full Title: Double blind randomised controlled trial of Levosimendan versus Dopexamine in septic shock | ||
Medical condition: Septic Shock | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2008-000818-78 | Sponsor Protocol Number: 7-010-MR | Start Date*: 2008-09-25 | |||||||||||
Sponsor Name:POLICLINICO SAN DONATO IRCSS | |||||||||||||
Full Title: Efficacy of fenoldopam mesilate in controlling splanchnic ischemia during cardiopulmonary bypass | |||||||||||||
Medical condition: Patients to be submitted to cardiac surgery with expected prolonged CPB time | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-004412-38 | Sponsor Protocol Number: 1160.248 | Start Date*: 2017-01-09 | |||||||||||
Sponsor Name:Unilfarma - União Internacional de Lab. Farmacêuticos, Lda | |||||||||||||
Full Title: RE-SPECT CVT: a randomised, open-label, exploratory trial with blinded endpoint adjudication (PROBE), comparing efficacy and safety of oral dabigatran etexilate versus oral warfarin in patients wit... | |||||||||||||
Medical condition: cerebral vein and dural sinus thrombosis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: PT (Completed) NL (Completed) ES (Completed) DE (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-005162-29 | Sponsor Protocol Number: RivaSVT100 | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:A.O. OSPEDALE DI CIRCOLO E FONDAZIONE MACCHI | |||||||||||||
Full Title: Treatment of portal, mesenteric, and splenic vein thrombosis with rivaroxaban. A pilot, prospective cohort study | |||||||||||||
Medical condition: Portal, mesenteric, and splenic vein thrombosis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) NL (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-003093-40 | Sponsor Protocol Number: FADOI_032016 | Start Date*: 2017-03-10 |
Sponsor Name:FONDAZIONE FADOI | ||
Full Title: Apixaban for the treatment of venous thromboembolism in patients with cancer: a prospective randomized open blinded end point (PROBE) study- the CARAVAGGIO study. | ||
Medical condition: Venous thromboembolism in cancer patients | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FR (Completed) BE (Completed) GB (GB - no longer in EU/EEA) DE (Completed) ES (Completed) PT (Completed) PL (Completed) NL (Completed) IT (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2012-002890-71 | Sponsor Protocol Number: RifaxNK150612 | Start Date*: 2012-08-16 | |||||||||||
Sponsor Name:Flemming Bendtsen | |||||||||||||
Full Title: Intestinal decontamination with rifaximin. Effects on the inflammatory and circulatory state in patients with cirrhosis and ascites - A randomised controlled clinical study | |||||||||||||
Medical condition: Liver cirrhosis of any etilogy, complicated by decompensation and classified as Child-Pugh B or C | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-000833-12 | Sponsor Protocol Number: POLYCHEM | Start Date*: Information not available in EudraCT |
Sponsor Name:Azienda Ospedaliero-Universitaria di Parma | ||
Full Title: A prospective, randomized, parallel-group, adaptive design phase IIb/III, multicenter study, to assess the efficacy of polychemotherapy for inducing remission of newly diagnosed type 2 diabetes. | ||
Medical condition: type 2 diabetes mellitus | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: IT (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2010-019500-23 | Sponsor Protocol Number: MPD-RC111 | Start Date*: 2012-02-15 | ||||||||||||||||
Sponsor Name:CONSORZIO MARIO NEGRI SUD | ||||||||||||||||||
Full Title: Single Arm Salvage Therapy with Pegylated Interferon Alfa-2a for Patients with High Risk Polycythemia Vera or High Risk Essential Thrombocythemia who are Either Hydroxyurea Resistant or Intolerant ... | ||||||||||||||||||
Medical condition: High risk polycythemia vera and high risk essential thrombocythemia | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: IT (Ongoing) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-001230-18 | Sponsor Protocol Number: PRO-001 | Start Date*: 2019-01-30 | |||||||||||
Sponsor Name:Hellenic Genito-Urinary Cancer Group (HGUCG) | |||||||||||||
Full Title: Long-term thromboprophylaxis with tinzaparin in high-risk prostate or breast cancer patients. A prospective, randomised, international multicentre, open-label, blinded-endpoint Phase III study. PRO... | |||||||||||||
Medical condition: Long-term thromboprophylaxis with tinzaparin in high-risk prostate or breast cancer patients. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GR (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-006694-91 | Sponsor Protocol Number: FARM6YNXAN | Start Date*: 2008-05-23 | |||||||||||
Sponsor Name:G.I.M.E.M.A. | |||||||||||||
Full Title: A large-scale trial testing the intensity of CYTOreductive therapy to prevent cardiovascular events In patients with Polycythemia Vera (PV) CYTO-PV. | |||||||||||||
Medical condition: Polycytemia vera | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-002298-25 | Sponsor Protocol Number: 20203331 | Start Date*: 2021-09-15 |
Sponsor Name:Fundación para la Investigación Biomédica del Hospital Universitario La Paz (FIBHULP) | ||
Full Title: A multicenter, adaptive, prospective, randomized trial evaluating the efficacy and safety of antithrombotic strategies in patients with COVID-19 following hospital discharge | ||
Medical condition: COVID-19 | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2020-001709-21 | Sponsor Protocol Number: 2020PI073 | Start Date*: 2020-04-29 | |||||||||||
Sponsor Name:CHRU de Nancy | |||||||||||||
Full Title: Effectiveness of low molecular weight heparin at increased doses prophylaxis weight-adjusted, compared with lower doses prophylaxis (intermediate or standard), on the onset of venous thromboembolis... | |||||||||||||
Medical condition: Prevention of thromboembolic events in hospitalised COVID-19 infected patients | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-002606-20 | Sponsor Protocol Number: CV185-325/B0661037 | Start Date*: 2015-11-06 | |||||||||||
Sponsor Name:Bristol-Myers Squibb International Corporation | |||||||||||||
Full Title: A RANDOMIZED, OPEN-LABEL, ACTIVE CONTROLLED, SAFETY AND DESCRIPTIVE EFFICACY STUDY IN PEDIATRIC SUBJECTS REQUIRING ANTICOAGULATION FOR THE TREATMENT OF A VENOUS THROMBOEMBOLIC EVENT | |||||||||||||
Medical condition: Venous Thromboembolism | |||||||||||||
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Population Age: Preterm newborn infants, Newborns, Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) Outside EU/EEA AT (Completed) GB (GB - no longer in EU/EEA) ES (Ongoing) PT (Completed) IT (Not Authorised) FR (Ongoing) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-005624-10 | Sponsor Protocol Number: OVID-trial | Start Date*: 2021-05-06 | ||||||||||||||||
Sponsor Name:University Hospital Zurich | ||||||||||||||||||
Full Title: ENOXAPARIN FOR PRIMARY THROMBOPROPHYLAXIS IN AMBULATORY PATIENTS WITH CORONAVIRUS: THE MULTICENTER RANDOMIZED CONTROLLED OVID TRIAL | ||||||||||||||||||
Medical condition: Patients diagnosed with COVID-19, a novel viral disease characterized by severe systemic, pulmonary, and vessel inflammation and coagulation activation. | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Prematurely Ended) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-005530-42 | Sponsor Protocol Number: imPaCT-PRO-01 | Start Date*: 2021-12-07 | ||||||||||||||||
Sponsor Name:Institute of Molecular Medicine and Biomedical Research (IMBE) | ||||||||||||||||||
Full Title: The impact of Thromboprophylaxis on Progression Free Survival of Patients with Advanced Pancreatic Cancer. The Pancreatic Cancer & Tinzaparin Prospective (imPaCT-PRO) study | ||||||||||||||||||
Medical condition: Thromboprophylaxis in patients with advanced pancreatic cancer | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: GR (Trial now transitioned) | ||||||||||||||||||
Trial results: (No results available) |
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