- Trials with a EudraCT protocol (8)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
8 result(s) found for: Laryngeal mask airway.
Displaying page 1 of 1.
EudraCT Number: 2014-003810-96 | Sponsor Protocol Number: 14-073 | Start Date*: 2015-01-15 |
Sponsor Name:RWTH Aachen University for the Medical Falculty, represented by Clinical Trial Center Aachen (CTC-A) | ||
Full Title: Emergence times and airway reactions in general laryngeal mask airway anesthesia: a randomized multicenter controlled trial | ||
Medical condition: Under investigation are first the time a patient needs to emerge from anesthesia (stating the date of birth) and second the occurrence of airway complications. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2012-004163-50 | Sponsor Protocol Number: FIBHGM-ECNC002-2013(CETSEVOREM) | Start Date*: 2014-04-29 | |||||||||||
Sponsor Name:Fundación para la Investigación Biomédica del Hospital | |||||||||||||
Full Title: Comparative, randomized, double-blind clinical trial on end-tidal concentration of sevoflurane associated to remifentanil required for insertion of the Supreme Laryngeal Mask vs. Pro-Seal Laryngea... | |||||||||||||
Medical condition: Patients requiring general anesthesia in whom the control of the airway is usually done with a supraglottic device. | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-002009-37 | Sponsor Protocol Number: 0517 | Start Date*: 2017-07-14 | |||||||||||
Sponsor Name:Neuroanæstesiologisk Klinik, RH/Glostrup | |||||||||||||
Full Title: "The effect of Betamethasone gel and NSAID gel lubricated on the laryngeal mask on pain in the throat, hoarseness and cough after anesthesia. " | |||||||||||||
Medical condition: 'Healthy volunteers' (sore throat, hoarseness and cough, consumption of analgesics, postoperative itching, numbness and burning sensation from the throat) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
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: 2010-019420-31 | Sponsor Protocol Number: no sponser | Start Date*: 2011-04-22 |
Sponsor Name: | ||
Full Title: ‘The influence of MAC values and behaviour of a child on emergence delirium after sevoflurane anaesthesia’ | ||
Medical condition: ‘Emergence delirium’ (ED) is described as a mental disorder during recovery from general anaesthesia. After the introduction of new inhalation anaesthetics such as sevoflurane, this phenomenon agai... | ||
Disease: | ||
Population Age: Infants and toddlers, Children, Under 18 | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2004-004721-10 | Sponsor Protocol Number: | Start Date*: 2005-05-25 |
Sponsor Name:Sussex NHS Research Consortium, Research Department, Worthing Hospital | ||
Full Title: | ||
Medical condition: Proximal femoral fracture | ||
Disease: | ||
Population Age: Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2022-002947-23 | Sponsor Protocol Number: DP10027 | Start Date*: 2023-04-14 | |||||||||||
Sponsor Name:Acacia Pharma Ltd | |||||||||||||
Full Title: Randomized, double-blind, Phase 2/3 study of IV amisulpride as prevention of post-operative nausea and vomiting in pediatric patients | |||||||||||||
Medical condition: post-operative nausea and vomiting in pediatric patients | |||||||||||||
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Population Age: Newborns, Infants and toddlers, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-001091-18 | Sponsor Protocol Number: FIBHGM-ECNC002-2011 | Start Date*: 2011-09-20 | |||||||||||
Sponsor Name:Fundación para la Investigación Biomédica del Hospital Gregorio Marañón | |||||||||||||
Full Title: Comparative, randomized, double-blind clinical trial on 50 effective plasma concentration of propofol required for insertion of the Supreme Laryngeal Mask with or without association of remifenta... | |||||||||||||
Medical condition: Patients requiring general anesthesia in whom the control of the airway is usually done with a supraglottic device. | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
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