- Trials with a EudraCT protocol (1,147)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (1,641)
1,147 result(s) found for: Anesthesia.
Displaying page 1 of 58.
EudraCT Number: 2021-001854-74 | Sponsor Protocol Number: RBHP-2021-ELJEZI | Start Date*: 2021-07-28 | ||||||||||||||||
Sponsor Name:CHU de Clermont-Ferrand | ||||||||||||||||||
Full Title: - | ||||||||||||||||||
Medical condition: - | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: FR (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-000922-31 | Sponsor Protocol Number: Cognitivefunction2011001 | Start Date*: 2011-04-18 | |||||||||||
Sponsor Name:Karolinska Institutet | |||||||||||||
Full Title: Patients´ recovery day 0-3 after short-stay elective surgery – a pilot study comparing desflurane and propofol TCI as main anaesthetics. | |||||||||||||
Medical condition: Patients undergoing elective general anaesthesia for breat surgery | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: SE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-006037-41 | Sponsor Protocol Number: CISN2O | Start Date*: 2006-12-21 | |||||||||||
Sponsor Name:Klaus Olkkola | |||||||||||||
Full Title: Interaction of cisatracurium with nitrous oxide as quantified by closed-loop feedback control / Typpioksiduulin vaikutus sisatrakuurin annostarpeeseen käytettäessä sisatrakuurin tietokoneohjattua a... | |||||||||||||
Medical condition: Tutkimuksen kohderyhmänä ovat potilaat, joille tehdään yleisanestesiaa vaativa leikkaus, jonka kesto on vähintään 90 min. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-003498-13 | Sponsor Protocol Number: HIP/FUSION#1 | Start Date*: 2016-03-18 | |||||||||||
Sponsor Name:Institut for Klinisk Medicin, Aarhus Universitet | |||||||||||||
Full Title: Surgical anesthesia for elective hip surgery - hemodynamic effect of lumbosacral plexus blockade compared to continuous spinal anesthesia | |||||||||||||
Medical condition: No specific medical condition is investigated. The objective of the investigation is to compare two methods for surgical anesthesia for total hip replacement. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-004343-76 | Sponsor Protocol Number: NMBA_ELDERLY2019ROCU_DOSES | Start Date*: 2020-02-27 | |||||||||||
Sponsor Name:Rigshospitalet | |||||||||||||
Full Title: A single-blinded multicenter randomized interventional study of rocuronium 0.3 mg/kg, and 0.9 mg/kg comparing onset time, duration of action and effect on intubating conditions in elderly patients ... | |||||||||||||
Medical condition: The aim of this study is to determine the onset time, duration of action and effect on intubating conditions after rocuronium 0.3 mg/kg and 0.9 mg/kg in patients with age ≥ 80 years. | |||||||||||||
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Population Age: Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-001534-34 | Sponsor Protocol Number: 260319 | Start Date*: 2022-03-11 | |||||||||||
Sponsor Name:Odense University Hospital | |||||||||||||
Full Title: Propofol and thiopental for intravenous induction in neonates: a dose finding study | |||||||||||||
Medical condition: Any condition requiring general anesthesia. | |||||||||||||
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Population Age: Preterm newborn infants, Newborns, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-000846-20 | Sponsor Protocol Number: ANE-INTRA-2013 | Start Date*: 2013-06-24 | |||||||||||
Sponsor Name:Fundació Parc Taulí | |||||||||||||
Full Title: Comparison of the effects of bupivacain or levobupivacain on cerebral oxigenation during intradural anesthesia in elderly patients who undergo major orthopaedic surgery for hip replacement | |||||||||||||
Medical condition: Intradural anaesthesia | |||||||||||||
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Population Age: Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-000702-71 | Sponsor Protocol Number: PreSpiDi2006-01 | Start Date*: 2007-07-13 | ||||||||||||||||
Sponsor Name:Alysis Zorggroep | ||||||||||||||||||
Full Title: The effect of intravenous fluid preload on diuresis during spinal anesthesia-induced detrusor blockade | ||||||||||||||||||
Medical condition: Diuresis during spinal anesthesia | ||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: NL (Ongoing) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-016094-16 | Sponsor Protocol Number: AGO/2009/008 | Start Date*: 2010-02-04 | |||||||||||
Sponsor Name:University Hospital Ghent | |||||||||||||
Full Title: Sevoflurane-Remifentanil interaction: Multiple response surfaces, validation of calibration stimuli, validation of the intraoperative isobole concept and investigating remifentanil induced opioid t... | |||||||||||||
Medical condition: American Society of Anesthesia class I and II patients scheduled for surgery under general anesthesia. | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-013892-23 | Sponsor Protocol Number: 1A-RSI-SU | Start Date*: 2009-08-19 | |||||||||||||||||||||
Sponsor Name:Rigshospitalet | |||||||||||||||||||||||
Full Title: ”Akut indledning” med Rocuronium-Sugammadex sammenlignet med Suxamethon | |||||||||||||||||||||||
Medical condition: Akut indledning ved universel anæstesi | |||||||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: DK (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2008-008193-31 | Sponsor Protocol Number: 2008/44 | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:Hopital Foch | |||||||||||||
Full Title: Impact des facteurs chronologiques et démographiques sur les posologies per-opératoires des agents anesthésiques (Etude prospective multicentrique) | |||||||||||||
Medical condition: general anesthesia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-007179-26 | Sponsor Protocol Number: 2008/41 | Start Date*: 2009-02-13 | |||||||||||
Sponsor Name:Hopital Foch | |||||||||||||
Full Title: Evaluation de l’effet anesthésique de la dexmédétomidine dans une population d’opérés recevant une anesthésie totale intraveineuse en « boucle » guidée par l’index bispectral (Etude monocentrique, ... | |||||||||||||
Medical condition: general anesthesia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: FR (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-002824-98 | Sponsor Protocol Number: ANE_HEPUNOX | Start Date*: 2016-10-20 | |||||||||||
Sponsor Name:Fundació Hospital Vall Hebron Institut de Recerca | |||||||||||||
Full Title: Comparison of three techniques in the management of the postoperatory acute pain, after a general anesthesia based on the control of the nociception. | |||||||||||||
Medical condition: Acute postoperative pain | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-005382-14 | Sponsor Protocol Number: SUH-TQL-QUADRICEPS | Start Date*: 2021-08-16 | |||||||||||
Sponsor Name:Associate Professor, Consultant Jens Børglum | |||||||||||||
Full Title: Does administration of the Transmuscular Quadratus lumborum block cause quadriceps muscle weakness? A randomised double-blinded volunteer study | |||||||||||||
Medical condition: Healthy volunteers (to investigate potential quadriceps muscle weakness following administration of a Transmuscular Quadratus Lumborum block) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-004242-10 | Sponsor Protocol Number: MM1-2020 | Start Date*: 2020-12-21 | |||||||||||||||||||||||||||||||||||||||||
Sponsor Name:Centre for Anaesthesiological Research, Department of Anaesthesiology, Zealand University Hospital, Køge, Denmark | |||||||||||||||||||||||||||||||||||||||||||
Full Title: Does perineural dexamethasone increase the duration of an ulnar nerve block when controlling for systemic effects? A randomised, blinded, placebo-controlled, paired, non-inferiority trial in health... | |||||||||||||||||||||||||||||||||||||||||||
Medical condition: We will not assess a specific medical condition or disease as only healthy volunteers are included. We will assess if perineural dexamethasone increases the duration of a peripheral nerve block (i.... | |||||||||||||||||||||||||||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||||||||||||||||||||||||||||||||
Trial protocol: DK (Completed) | |||||||||||||||||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2006-003515-44 | Sponsor Protocol Number: ACA-SPAI-04-22 | Start Date*: 2006-12-26 | |||||||||||
Sponsor Name:FRANCISCO JAVIER BELDA | |||||||||||||
Full Title: Cardioprotective effect of sevoflurane versus propofol used during anesthesia and the postoperative period in patients undergoing coronary bypass surgery. Impact on critical care unit stay. A doubl... | |||||||||||||
Medical condition: This study will evaluate the cardioprotective effects of sevoflurane versus propofol during anesthesia and sedation of patients undergoing coronary bypass surgery in terms of maintenance of cardiac... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-003172-36 | Sponsor Protocol Number: 29.06.2011 | Start Date*: 2011-10-07 | |||||||||||||||||||||
Sponsor Name:Department of Anaesthesia, Tampere University Hospital | |||||||||||||||||||||||
Full Title: Arousal reaction during desflurane anaesthesia | |||||||||||||||||||||||
Medical condition: The patients who undergo abdominal surgeries (laparotomy or laparoscopy) under desflurane anaesthesia will be investigated. | |||||||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: FI (Prematurely Ended) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-001493-32 | Sponsor Protocol Number: RC 16/07 | Start Date*: 2008-06-09 | |||||||||||
Sponsor Name:ISTITUTO PER L'INFANZIA BURLO GAROFOLO | |||||||||||||
Full Title: Comparison between two different sedation strategies (propofol versus propofol plus ketamine) in deep sedation managed by non anesthesiologists. | |||||||||||||
Medical condition: Procedural deep sedation (gastrointestinal endoscopy, lumbar puncture, etc) | |||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-000189-71 | Sponsor Protocol Number: RBHP2015BAZIN | Start Date*: 2015-03-27 | |||||||||||
Sponsor Name:CHU de Clermont-Ferrand | |||||||||||||
Full Title: . | |||||||||||||
Medical condition: . | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-012898-36 | Sponsor Protocol Number: 2009/22 | Start Date*: 2009-09-21 | |||||||||||
Sponsor Name:Hopital Foch | |||||||||||||
Full Title: Relation dose-effet du propofol : comparaison en double aveugle des différentes | |||||||||||||
Medical condition: general anesthesia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Ongoing) | |||||||||||||
Trial results: (No results available) |
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