- Trials with a EudraCT protocol (12)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
12 result(s) found for: Propofol Infusion Syndrome.
Displaying page 1 of 1.
EudraCT Number: 2012-000584-25 | Sponsor Protocol Number: FLAM01 | Start Date*: 2012-03-29 |
Sponsor Name:UZBrussel | ||
Full Title: Propofol and etomidate. Are they also safe for patients with Brugada-Syndrome? | ||
Medical condition: Patients suspected to have Brugada Syndrome | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: View results |
EudraCT Number: 2019-004750-28 | Sponsor Protocol Number: PropoCon-Pilot | Start Date*: 2021-04-30 |
Sponsor Name:Universitair Ziekenhuis Brussel | ||
Full Title: Electrocardiographic And Clinical Effects Of Target-Controlled Infusion Of Propofol In Adults With Brugada Syndrome. A Pilot Study. | ||
Medical condition: Target Controlled Infusion of Propofol in patients with Brugada Syndrome. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2014-000868-17 | Sponsor Protocol Number: DEXPROPAR | Start Date*: 2014-06-26 | |||||||||||
Sponsor Name:Clínica Universidad de Navarra/Universidad de Navarra | |||||||||||||
Full Title: Effect of dexmedetomidine vs propofol on basal ganglia activity (local field potentials) recorded through implanted stimulators | |||||||||||||
Medical condition: Parkinson's disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-002876-41 | Sponsor Protocol Number: 38RC18.123 | Start Date*: Information not available in EudraCT |
Sponsor Name:CHU Grenoble-Alpes | ||
Full Title: Assesment of Propofol sedation during intra tracheal surfactant administration by the LISA method (Less Invasive Surfactant Administration) | ||
Medical condition: Respiratory Distress Syndrome of preterm babies born < 32 weeks of gestational age | ||
Disease: | ||
Population Age: Preterm newborn infants, Under 18 | Gender: Male, Female | |
Trial protocol: FR (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2022-003638-38 | Sponsor Protocol Number: FIM-SEV-2022-01 | Start Date*: 2023-04-10 | |||||||||||
Sponsor Name:FIMABIS | |||||||||||||
Full Title: CARDIOPROTECTIVE-NEPHROPROTECTIVE EFFECTS OF SEVOFLURAN IN COMPARISON WITH PROPOFOL IN DOUBLE VALVULAR SURGERY. USE OF SEVOFLURANE AS A PILLAR OF PROTECTION IN EXTRACORPOREA CIRCULATION AND POSTOPE... | |||||||||||||
Medical condition: DOBLE VALVE SURGERY | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-001113-32 | Sponsor Protocol Number: CNS7056-010 | Start Date*: 2013-08-02 | |||||||||||
Sponsor Name:PAION UK Limited | |||||||||||||
Full Title: A Randomized, Single-blind Phase II Study Evaluating the Efficacy, Safety and Pharmacokinetics of Remimazolam in General Anesthesia in Adult Patients Undergoing Cardiac Surgery, Including Follow-up... | |||||||||||||
Medical condition: Anaesthesia in adult patients undergoing cardiac surgery. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-004698-15 | Sponsor Protocol Number: S60859 | Start Date*: 2021-05-03 |
Sponsor Name:UZ Leuven / KU Leuven | ||
Full Title: Brain Injury and Ketamine: a prospective, randomized controlled double blind clinical trial to study the effects of ketamine on Therapy Intensity Level and intracranial pressure in acute brain inju... | ||
Medical condition: Traumatic Brain Injury patients requiring sedation to control the intracranial pressure (ICP). | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2011-001490-40 | Sponsor Protocol Number: 3005019 | Start Date*: 2012-04-03 | ||||||||||||||||
Sponsor Name:ORION CORPORATION ORION PHARMA | ||||||||||||||||||
Full Title: Comparative evaluation of the effects of dexmedetomidine and propofol on patient/ventilator interaction in difficult-to-wean mechanically ventilated patients; a prospective, open, randomised, mul... | ||||||||||||||||||
Medical condition: Patients requiring mechanical ventilation and sedation in the ICU | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: IT (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2019-004537-16 | Sponsor Protocol Number: 29BRC19.0280 | Start Date*: 2020-03-26 | |||||||||||
Sponsor Name:CHRU de Brest | |||||||||||||
Full Title: Comparison of an inhaled sedation strategy to an intravenous sedation strategy in ICU patients treated with invasive mechanical ventilation | |||||||||||||
Medical condition: Prevention of delirium | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-000171-16 | Sponsor Protocol Number: KCH-PRO:19/001 | Start Date*: 2019-08-02 | |||||||||||
Sponsor Name:King's College Hospital NHS Foundation Trust | |||||||||||||
Full Title: Comparison between Propofol and Inhalational Anaesthetic Agents on Cardiovascular Outcomes following Cardiac Surgery - a Randomised Controlled Feasibility Trial | |||||||||||||
Medical condition: Cardiopulmonary bypass (CPB) and revascularisation-induced ischaemic reperfusion injury | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-002188-13 | Sponsor Protocol Number: UoL001087 | Start Date*: 2015-03-03 | |||||||||||
Sponsor Name:University of Liverpool [...] | |||||||||||||
Full Title: Emergency Treatment with Levetiracetam or Phenytoin in Status Epilepticus in Children (EcLiPSE) – an open label randomised controlled trial | |||||||||||||
Medical condition: Convulsive Status Epilepticus | |||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-001752-43 | Sponsor Protocol Number: SEVO-AIFA-FARM6H73Z9 | Start Date*: 2008-07-17 | |||||||||||
Sponsor Name:OSPEDALE S. RAFFAELE | |||||||||||||
Full Title: CARDIAC PROTECTION WITH SEVOFLURANE IN PATIENTS WITH HIGH RISK UNDERGOING HEART SURGERY. RANDOMIZED, CONTROLLED STUDY. | |||||||||||||
Medical condition: adult patients affected by cardiac valve and heart patology undergoing elective surgery | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
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