- Trials with a EudraCT protocol (140)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
140 result(s) found for: Septic Shock.
Displaying page 1 of 7.
EudraCT Number: 2007-000513-12 | Sponsor Protocol Number: NR 9284-3 | Start Date*: 2007-02-15 | |||||||||||
Sponsor Name:Úrazová nemocnice brno | |||||||||||||
Full Title: Terlipressin in the treatment of catecholamine-resistant septic shock | |||||||||||||
Medical condition: Septic shock refractory to standard dose of norepinephrine | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-001254-26 | Sponsor Protocol Number: 000025 | Start Date*: 2012-06-07 | |||||||||||
Sponsor Name:Ferring Pharmaceuticals A/S | |||||||||||||
Full Title: An open label feasibility trial investigating FE 202158 as potential primary vasopressor treatment in patients with vasodilatory hypotension in early septic shock | |||||||||||||
Medical condition: Hypotension in early septic shock | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-001613-33 | Sponsor Protocol Number: IgM-FAT | Start Date*: 2019-04-18 | |||||||||||||||||||||
Sponsor Name:AZIENDA OSPEDALIERO-UNIVERSITARIA DI MODENA | |||||||||||||||||||||||
Full Title: Efficacy and safety of adjunctive IgM-enriched immunoglobulin therapy with a personalized dose based on serum IgM-titers vs. standard dose in patients with septic shock. A multicenter, intervention... | |||||||||||||||||||||||
Medical condition: Septic shock | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: IT (Trial now transitioned) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-003012-31 | Sponsor Protocol Number: 2011RC23r | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:DIRECTION CENTRALE DU SERVICE DE SANTE DES ARMEES | |||||||||||||
Full Title: Cardiovascular effects of esmolol alone and in combination with levosimendan during septic shock | |||||||||||||
Medical condition: | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-007971-18 | Sponsor Protocol Number: LOC/05-12/RENNES | Start Date*: 2008-03-18 | |||||||||||||||||||||
Sponsor Name:C.H.U. de RENNES | |||||||||||||||||||||||
Full Title: Evaluation des effets de la 9 alpha fluorohydrocortisone sur la réponse pressive à la noradrénaline, la perfusion gastrique, le débit huméral et la rigidité artérielle dans le choc septique. | |||||||||||||||||||||||
Medical condition: Choc septique. | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: FR (Ongoing) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-003158-10 | Sponsor Protocol Number: GI-CCT372273 | Start Date*: 2014-04-11 | |||||||||||
Sponsor Name:The George Institute for Global Health | |||||||||||||
Full Title: ADRENAL- ADjunctive coRticosteroid trEatment iN criticAlly ilL patients with septic shock. | |||||||||||||
Medical condition: Septic Shock | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) DK (Completed) IE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-010798-19 | Sponsor Protocol Number: FE202158CS02 | Start Date*: 2009-10-12 | |||||||||||
Sponsor Name:Ferring Pharmaceuticals A/S | |||||||||||||
Full Title: A randomized, double-blind, placebo-controlled, infusion proof-of-concept trial investigating the safety, tolerability, pharmacokinetics, and pharmacodynamics of ascending doses of FE 202158 in pat... | |||||||||||||
Medical condition: Vasodilatory hypotension in early septic shock | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-017825-21 | Sponsor Protocol Number: EC09/081 | Start Date*: 2012-11-19 | |||||||||||
Sponsor Name:INSTITUTO ARAGONÉS DE CIENCIAS DE LA SALUD | |||||||||||||
Full Title: Prospective, randomised, double-blind study to evaluate the efficacy of treatment with melatonin in adult patients with severe sepsis or septic shock. | |||||||||||||
Medical condition: Severe sepsis or septic shock. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-000427-27 | Sponsor Protocol Number: VIPER-SHOCK | Start Date*: 2017-03-30 | |||||||||||
Sponsor Name:Section for Transfusion Medicine, Capitol Region Blood Bank | |||||||||||||
Full Title: Vasculopathic Injury and Plasma as Endothelial Rescue in septic shock (SHOCK) trial | |||||||||||||
Medical condition: Patients with septic shock admitted to the intensive care unit. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-005363-24 | Sponsor Protocol Number: CRO1888 | Start Date*: 2012-12-05 | |||||||||||
Sponsor Name:Imperial College London | |||||||||||||
Full Title: Vasopressin vs Noradrenaline as Initial therapy in Septic Shock | |||||||||||||
Medical condition: Septic Shock | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-003973-41 | Sponsor Protocol Number: 000133 | Start Date*: 2015-06-22 | |||||||||||
Sponsor Name:Ferring Pharmaceuticals A/S | |||||||||||||
Full Title: A Double-blind, Randomised, Placebo-controlled, Phase 2b/3 Adaptive Clinical Trial Investigating the Efficacy and Safety of Selepressin as Treatment for Patients with Vasopressor-dependent Septic S... | |||||||||||||
Medical condition: Vasopressor-dependent Septic Shock | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) NL (Completed) FR (Completed) DK (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-004827-36 | Sponsor Protocol Number: MOT-C-203 | Start Date*: 2019-08-07 | |||||||||||
Sponsor Name:INOTREM S.A. | |||||||||||||
Full Title: Efficacy, Safety and Tolerability of Nangibotide in Patients with Septic Shock. A Randomized, Double-blind, Placebo Controlled Dose Selection Study. | |||||||||||||
Medical condition: Septic shock | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) FR (Completed) ES (Ongoing) DK (Completed) FI (Completed) IE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-000707-81 | Sponsor Protocol Number: VIPER-SEPSIS | Start Date*: 2016-04-26 | |||||||||||
Sponsor Name:Section for Transfusion Medicine, Capitol Region Blood Bank | |||||||||||||
Full Title: Vasculopathic Injury and Plasma as Endothelial Rescue in septic shock (SEPSIS) trial | |||||||||||||
Medical condition: Patients with septic shock admitted to the intensive care unit | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-005441-38 | Sponsor Protocol Number: F1K-MC-EVDP | Start Date*: 2008-03-07 | |||||||||||
Sponsor Name:Eli Lilly and Company | |||||||||||||
Full Title: Efficacy and Safety of Drotrecogin Alfa (Activated) in Adult Patients with Septic Shock | |||||||||||||
Medical condition: Septic shock | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) GB (Completed) NL (Completed) FR (Completed) BE (Completed) IT (Completed) PT (Completed) FI (Completed) CZ (Completed) ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2022-003846-10 | Sponsor Protocol Number: MJIP1.0 | Start Date*: 2024-05-02 | |||||||||||
Sponsor Name:Fakultní nemocnice Plzeň | |||||||||||||
Full Title: A pilot study comparing the haemodynamic effects and safety of an intravenous fluid bolus of 0.5M sodium lactate against 3% saline in patients with septic shock | |||||||||||||
Medical condition: Septic shock fluid treatment | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-001131-31 | Sponsor Protocol Number: COMBAT-SHINE | Start Date*: 2019-06-25 | |||||||||||
Sponsor Name:Section for transfusion Medicines, Capital Region Blood Bank, Copenhagen University Hospital | |||||||||||||
Full Title: “Efficacy and safety of 72-hour infusion of Prostacyclin (1 ng/kg/min) in patients with septic shock induced endotheliopathy – a multicentre randomized, placebo-controlled, blinded, investigator-in... | |||||||||||||
Medical condition: Shock-induced endotheliopathy in patients with septic shock | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-002440-41 | Sponsor Protocol Number: CO-ILEPSS | Start Date*: 2014-08-14 | |||||||||||
Sponsor Name:Rigshospitalet, Capital Region Bloodbank 2034, Section for Transfusion Medicine | |||||||||||||
Full Title: Safety and efficacy of iloprost and eptifibatide co-administration compared to standard therapy in patients with septic shock – a randomized, controlled, double-blind investigator-initiated trial | |||||||||||||
Medical condition: Septic shock | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-000504-92 | Sponsor Protocol Number: APX-PHP-07-008 | Start Date*: 2009-09-02 | |||||||||||
Sponsor Name:Apex Bioscience, Inc. | |||||||||||||
Full Title: PHP for the Treatment of Excess Nitric Oxide in Distributive Shock (PHOENIX) | |||||||||||||
Medical condition: Catecholamine-resistant distributive shock | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Prematurely Ended) DE (Prematurely Ended) AT (Prematurely Ended) BE (Prematurely Ended) GB (Prematurely Ended) ES (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-005032-14 | Sponsor Protocol Number: MOT-C-201 | Start Date*: 2017-04-27 | |||||||||||
Sponsor Name:INOTREM S.A. | |||||||||||||
Full Title: Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of 3 Doses of MOTREM in Patients with Septic Shock. A Randomised, Double-blind, Two-stage, Placebo Controlled Study. | |||||||||||||
Medical condition: Septic shock | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) NL (Completed) ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2022-001949-20 | Sponsor Protocol Number: 1.0 | Start Date*: 2023-01-09 | |||||||||||
Sponsor Name:ALBIMMUNE S.L. | |||||||||||||
Full Title: Human albumin treatment in adult septic shock. A phase 2, multicenter, randomized, controlled study evaluating the immune response and organ failure. | |||||||||||||
Medical condition: Septic Shock | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: (No results available) |
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