- Trials with a EudraCT protocol (12)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
12 result(s) found for: Coma AND Cardiac Arrest.
Displaying page 1 of 1.
| EudraCT Number: 2013-004311-45 | Sponsor Protocol Number: 2013-PharmaCA-001 | Start Date*: 2014-03-25 | |||||||||||
| Sponsor Name:Copenhagen University Hospital Rigshospitalet, Department of Cardiology B 2143 | |||||||||||||
| Full Title: GLP-1 ANALOGS FOR NEUROPROTECTION AFTER OUT-OF-HOSPITAL CARDIAC ARREST, A RANDOMIZED CLINICAL TRIAL | |||||||||||||
| Medical condition: We investigate the efficacy of commercially available GLP-1 analog for reducing post anoxic brain injury in patients who remain comatose after having been resuscitation from out of hospital cardiac... | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DK (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2018-000005-23 | Sponsor Protocol Number: Ghreline | Start Date*: 2018-12-12 |
| Sponsor Name:University of Twente | ||
| Full Title: Ghrelin treatment of comatose patients after cardiac arrest: A clinical trial to promote cerebral recovery | ||
| Medical condition: Brain damage after cardiac arrest | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: NL (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2009-017499-26 | Sponsor Protocol Number: Heres | Start Date*: 2010-03-16 | ||||||||||||||||||||||||||
| Sponsor Name:Academical Medical Center, University of Amsterdam | ||||||||||||||||||||||||||||
| Full Title: The use of Helium after Resuscitation: a safety and feasibility study | ||||||||||||||||||||||||||||
| Medical condition: Persistent coma after cardiac arrest. | ||||||||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
| Trial protocol: NL (Ongoing) | ||||||||||||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||||||||||||
| EudraCT Number: 2015-002151-10 | Sponsor Protocol Number: NEUROPROTECTpost-CA | Start Date*: 2015-08-07 | |||||||||||
| Sponsor Name:UZ Leuven | |||||||||||||
| Full Title: Neuroprotective goal directed hemodynamic optimization in post-cardiac arrest patients: a randomized controlled trial (the NEUROPROTECT post-CA trial) | |||||||||||||
| Medical condition: post-cardiac arrest patients | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: BE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2017-004318-25 | Sponsor Protocol Number: NL63681.029.18 | Start Date*: 2019-04-16 | |||||||||||
| Sponsor Name:VU University Medical Center | |||||||||||||
| Full Title: Early high-dose vitamin C in post-cardiac arrest syndrome. | |||||||||||||
| Medical condition: Patients admitted to the Intensive Care after out-of-hospital cardiac arrest with return of spontaneous circulation, ventricular fibrillation or ventricular tachycardia as first registered cardiac ... | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: NL (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2017-002514-32 | Sponsor Protocol Number: NPT-CL-01 | Start Date*: 2018-09-12 | |||||||||||
| Sponsor Name:NeuroproteXeon, Inc. | |||||||||||||
| Full Title: XePOHCAS: Prospective, randomized, multicenter, interventional trial in adult subjects with out-of-hospital cardiac arrest (OHCA) comparing treatment with standard-of-care post-cardiac arrest inten... | |||||||||||||
| Medical condition: Post-cardiac arrest syndrome | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DK (Completed) DE (Ongoing) ES (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2022-002686-15 | Sponsor Protocol Number: CHUBX2021/25 | Start Date*: 2022-10-18 |
| Sponsor Name:CHU de Bordeaux | ||
| Full Title: Effectiveness of an Optimisation Strategy for Emergency Tracheal Intubation on postintubation Morbidity: A cluster randomized controlled trial | ||
| Medical condition: respiratory distress | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: FR (Trial now transitioned) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2009-011404-34 | Sponsor Protocol Number: P071217 | Start Date*: 2009-06-03 | |||||||||||
| Sponsor Name:ASSISTANCE PUBLIQUE - HOPITAUX DE PARIS (AP-HP) | |||||||||||||
| Full Title: Traitement par forte dose d'érythropoïétine après arrêt cardiaque : essai multicentrique contrôlé randomisé EPO-ACR 02 | |||||||||||||
| Medical condition: Réanimation post arrêt cardiaque | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2016-004072-22 | Sponsor Protocol Number: NINA-1 | Start Date*: 2017-12-07 | |||||||||||||||||||||||||||||||
| Sponsor Name:Norwegian University of Science and Technology (NTNU) | |||||||||||||||||||||||||||||||||
| Full Title: NTNU Intranasal Naloxone Trial Double blinded, double dummy, randomised controlled trial of intranasal naloxone for pre hospital use | |||||||||||||||||||||||||||||||||
| Medical condition: We investigate the reversal of opioid overdoses in the pre hospital setting | |||||||||||||||||||||||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||||||||||||||||||||||
| Trial protocol: NO (Completed) | |||||||||||||||||||||||||||||||||
| Trial results: View results | |||||||||||||||||||||||||||||||||
| EudraCT Number: 2011-005235-22 | Sponsor Protocol Number: ANZIC-RC/RB002 | Start Date*: 2012-01-18 | |||||||||||
| Sponsor Name:Monash University | |||||||||||||
| Full Title: A randomised, placebo-controlled trial of erythropoietin in ICU patients with traumatic brain injury: Erythropoietin in Traumatic Brain Injury | |||||||||||||
| Medical condition: Traumatic brain injury | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: FI (Completed) FR (Ongoing) DE (Ongoing) IE (Completed) | |||||||||||||
| 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: 2021-001453-31 | Sponsor Protocol Number: CONMED3 | Start Date*: Information not available in EudraCT | ||||||||||||||||
| Sponsor Name:Copenhagen University Hospital Rigshospitalet | ||||||||||||||||||
| Full Title: Automated pupillometry and NIRS-EEG to detect signatures of consciousness in acute brain injury after apomorphine and methylphenidate stimulation: A placebo-controlled, randomized, cross-over study | ||||||||||||||||||
| Medical condition: We investigate the possible effects of commercially available apomorphine and methylphenidate on signatures of consciousness in patients admitted to the ICU with acute disorder of consciousness, us... | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: DK (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
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