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Clinical trials for Sevoflurane

The European Union Clinical Trials Register   allows you to search for protocol and results information on:
  • interventional clinical trials that were approved in the European Union (EU)/European Economic Area (EEA) under the Clinical Trials Directive 2001/20/EC
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  • EU/EEA interventional clinical trials approved under or transitioned to the Clinical Trial Regulation 536/2014 are publicly accessible through the
    Clinical Trials Information System (CTIS).


    The EU Clinical Trials Register currently displays   44396   clinical trials with a EudraCT protocol, of which   7408   are clinical trials conducted with subjects less than 18 years old.   The register also displays information on   18700   older paediatric trials (in scope of Article 45 of the Paediatric Regulation (EC) No 1901/2006).

    Phase 1 trials conducted solely on adults and that are not part of an agreed paediatric investigation plan (PIP) are not publicly available (see Frequently Asked Questions ).  
     
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    97 result(s) found for: Sevoflurane. Displaying page 3 of 5.
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    EudraCT Number: 2008-005426-37 Sponsor Protocol Number: 4733 Start Date*: 2008-11-25
    Sponsor Name:University Medical Center Utrecht
    Full Title: The effect of sevoflurane and isoflurane on vasopressor need
    Medical condition: Aim of this study is to determine the effect of isoflurane versus sevoflurane on blood pressure and systemic vascular resistance.
    Disease: Version SOC Term Classification Code Term Level
    9.1 10005727 Blood pressure LLT
    9.1 10011978 Decreased systemic vascular resistance LLT
    Population Age: Adults, Elderly Gender: Male, Female
    Trial protocol: NL (Ongoing)
    Trial results: (No results available)
    EudraCT Number: 2015-004982-10 Sponsor Protocol Number: LOC-2016 Start Date*: 2015-12-15
    Sponsor Name:Harry Scheinin
    Full Title: The Neural Mechanisms of Anesthesia and Human Consciousness (Part 6)
    Medical condition: No medical condition or disease involved. The study subjects are healthy volunteers.
    Disease:
    Population Age: Adults Gender: Male
    Trial protocol: FI (Completed)
    Trial results: (No results available)
    EudraCT Number: 2014-002510-23 Sponsor Protocol Number: SR062014 Start Date*: 2014-09-17
    Sponsor Name:University hospitals of Leuven
    Full Title: as an adjuvant to sevoflurane anaesthesia in children undergoing interventional or diagnostic cardiac catheterization: a randomized controlled clinical trial
    Medical condition: Xenon anesthesia in children undergoing cardiac catheterization
    Disease:
    Population Age: Children, Under 18 Gender: Male, Female
    Trial protocol: BE (Completed)
    Trial results: View results
    EudraCT Number: 2015-002399-25 Sponsor Protocol Number: Sevo-Des-2015-01 Start Date*: 2015-11-04
    Sponsor Name:Servicio de Anestesia Infantil. Hospital Universitario La Paz
    Full Title: CLINICAL TRIAL TO COMPARE THE INCIDENCE AND CHARACTERISTICS OF POSTOPERATIVE AGITATION IN PEDIATRIC PATIENTS AFTER ANESTHESIA WITH SEVOFLURANE OR DESFLURANE IN AMBULATORY SURGERY.
    Medical condition: AGITATION AFTER POSTOPERATIVE ANESTHESIA IN PEDIATRIC PATIENTS
    Disease:
    Population Age: Infants and toddlers, Children, Under 18 Gender: Male, Female
    Trial protocol: ES (Ongoing)
    Trial results: (No results available)
    EudraCT Number: 2018-002258-56 Sponsor Protocol Number: SD-DXP Start Date*: 2018-08-27
    Sponsor Name:University Hospitals Leuven
    Full Title: The use of xenon and dexmedetomidine for the prevention of postoperative emergence delirium after anaesthesia for pediatric cardiac catheterization: A randomized, controlled, observer-blinded pilot...
    Medical condition: xenon-dexmedetomidine Anesthesia in children undergoing cardiac catheterization
    Disease:
    Population Age: Newborns, Infants and toddlers, Children, Under 18 Gender: Male, Female
    Trial protocol: BE (Completed)
    Trial results: View results
    EudraCT Number: 2005-005428-15 Sponsor Protocol Number: AGO/2005/003 Start Date*: 2006-01-30
    Sponsor Name:University Hospital Ghent
    Full Title: Vergelijkende studie tussen Propofol en Sevoflurane: sedatie en hemodynamiek postoperatief na electieve CABG (Coronair bypass chirurgie)
    Medical condition: postoperatieve anesthesie zorgen na electieve CABG
    Disease:
    Population Age: Adults, Elderly Gender: Male, Female
    Trial protocol: BE (Completed)
    Trial results: (No results available)
    EudraCT Number: 2004-004695-36 Sponsor Protocol Number: SEVAN Start Date*: 2004-12-16
    Sponsor Name:AZIENDA OSPEDALIERA SAN GERARDO DI MONZA
    Full Title: SEVOFLURANE SOMMINISTRED THROGH ANACONDA VERSUS PROPOFOL + REMIFENTANIL DURING THE SEDATION OF THE CRITICAL PATIENT INTUBATED AND VENTILATED IN THE INTENSIVE CARE UNIT
    Medical condition: SEDATION OF THE CRITICAL PATIENT INTUBATED AND VENTILATED IN ICU
    Disease:
    Population Age: Adults, Elderly Gender: Male, Female
    Trial protocol: IT (Completed)
    Trial results: (No results available)
    EudraCT Number: 2005-001574-27 Sponsor Protocol Number: MR-2005\01 Start Date*: 2005-09-27
    Sponsor Name:AZIENDA OSPEDALIERA DI PERUGIA
    Full Title: Sevoflurane on cardiac surgery: vantage to use during CEC
    Medical condition: general anestetic inalathory also during CEC
    Disease: Version SOC Term Classification Code Term Level
    6.1 10018060 PT
    Population Age: Adults, Elderly Gender: Male, Female
    Trial protocol: IT (Ongoing)
    Trial results: (No results available)
    EudraCT Number: 2012-004852-13 Sponsor Protocol Number: 2012001 Start Date*: 2014-06-24
    Sponsor Name:Anestesikliniken
    Full Title: Low fresh gas flow during elective general anaesthesia - A pilot study comparing Desflurane and Sevoflurane for anaesthetic controllability during wash-in and for haemodynamic control during elec...
    Medical condition: General anaesthesia time to onset - wash-in
    Disease:
    Population Age: Adults Gender: Male, Female
    Trial protocol: SE (Completed)
    Trial results: (No results available)
    EudraCT Number: 2004-004723-35 Sponsor Protocol Number: SEVO-DIP Start Date*: 2005-01-27
    Sponsor Name:OSPEDALE S. RAFFAELE DI MILANO
    Full Title: PRECONDITIONING EFFECT OF INALATORY ANESTHETICS
    Medical condition: SEVOFLURANE USED AS ANESTETIC IN ORDER TO OBTAIN A MYOCARDIAL PROTECTION
    Disease: Version SOC Term Classification Code Term Level
    14.1 10042613 - Surgical and medical procedures 10042613 Surgical and medical procedures SOC
    Population Age: Adults Gender: Male, Female
    Trial protocol: IT (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.
    Disease: Version SOC Term Classification Code Term Level
    16.1 100000004865 10018061 General anesthesia LLT
    Population Age: Adults Gender: Male, Female
    Trial protocol: ES (Completed)
    Trial results: (No results available)
    EudraCT Number: 2009-017153-35 Sponsor Protocol Number: ALMED-08-C2-020 Start Date*: 2010-04-06
    Sponsor Name:AIR LIQUIDE SANTE INTERNATIONAL
    Full Title: An international, multi-center, randomized, controlled trial evaluating the effect of xenon on post-operative delirium in elderly patients undergoing hip fracture surgery.
    Medical condition: Post-operative delirium after hip fracture surgery under general anaesthesia
    Disease: Version SOC Term Classification Code Term Level
    12.1 10020100 Hip fracture LLT
    Population Age: Elderly Gender: Male, Female
    Trial protocol: FR (Completed) DE (Completed) GB (Completed) ES (Completed) IT (Completed) BE (Completed)
    Trial results: View results
    EudraCT Number: 2022-002321-10 Sponsor Protocol Number: PR11/2022 Start Date*: 2023-01-16
    Sponsor Name:Hospital Universitari d'Igualada
    Full Title: Effectiveness and safety of topical sevoflurane for the treatment of painful skin ulcers; randomized, double-blind, placebo-controlled clinical trial
    Medical condition: Cutaneous complex ulcers (grade II, III and IV) which are painful and require hospital care
    Disease: Version SOC Term Classification Code Term Level
    20.0 100000004862 10065043 CMV mucocutaneous ulcer LLT
    21.0 100000004858 10045334 Ulcer skin LLT
    20.0 100000004858 10016980 Foot ulcer LLT
    20.0 100000004858 10077779 Pressure ulcer LLT
    21.0 100000004858 10077409 Ischemic skin ulcer LLT
    Population Age: Adults, Elderly Gender: Male, Female
    Trial protocol: ES (Ongoing)
    Trial results: (No results available)
    EudraCT Number: 2015-002329-20 Sponsor Protocol Number: SR052015 Start Date*: 2015-08-11
    Sponsor Name:University Hospitals Leuven
    Full Title: Xenon as an adjuvant to sevoflurane anaesthesia in children younger than four, undergoing interventional or diagnostic cardiac catheterization: a pilot study.
    Medical condition: Xenon anesthesia in children undergoing cardiac catherization
    Disease: Version SOC Term Classification Code Term Level
    18.0 100000004865 10018061 General anesthesia LLT
    Population Age: Infants and toddlers, Children, Under 18 Gender: Male, Female
    Trial protocol: BE (Completed)
    Trial results: View results
    EudraCT Number: 2016-003906-16 Sponsor Protocol Number: DESEVAR Start Date*: 2017-02-14
    Sponsor Name:Begoña Quintana
    Full Title: FAST-TRACK IN ENDOVASCULAR AORTIC ANEURYSM REPAIR WITH DESFLURANE AND SEVOFLURANE: A RANDOMIZED CLINICAL TRIAL
    Medical condition: AORTIC ANEURYSM
    Disease: Version SOC Term Classification Code Term Level
    19.1 100000004866 10002889 Aortic aneurysms and dissections HLT
    Population Age: Adults Gender: Male, Female
    Trial protocol: ES (Ongoing)
    Trial results: (No results available)
    EudraCT Number: 2011-003786-14 Sponsor Protocol Number: AGO/2011/006 Start Date*: 2011-12-20
    Sponsor Name:Ghent University Hospital
    Full Title: Heeft het toedienen van ketamine of sevoflurane bij kinderen van 0 tot 14 jaar een meerwaarde tijdens het verwijderen van chirurgische thoraxdrains?
    Medical condition:
    Disease: Version SOC Term Classification Code Term Level
    14.1 10042613 - Surgical and medical procedures 10067564 Anaesthesia procedure PT
    Population Age: Children, Adolescents, Under 18 Gender: Male, Female
    Trial protocol: BE (Completed)
    Trial results: View results
    EudraCT Number: 2017-000098-35 Sponsor Protocol Number: ANEPRO_2016_78 Start Date*: 2017-07-31
    Sponsor Name:SERVICIO DE ANESTESIOLOGÍA Y REANIMACIÓN HOSPITAL UNIVERSITARIO LA PAZ
    Full Title: COMPARATIVE STUDY OF NAUTICS AND VOMITING IN THREE ANESTHETICAL REGIMENS: INTRAVENOUS, INHALATORY AND MIXED.
    Medical condition: Arthroscopy for Temporomandibular
    Disease:
    Population Age: Adults, Elderly Gender: Male, Female
    Trial protocol: ES (Ongoing)
    Trial results: (No results available)
    EudraCT Number: 2009-015890-11 Sponsor Protocol Number: AGO/2009/007 Start Date*: 2009-11-03
    Sponsor Name:University Hospital Ghent
    Full Title: Conditioning with volatile anesthetics in liver transplantation
    Medical condition: Liver transplantation
    Disease: Version SOC Term Classification Code Term Level
    12.0 10024716 Liver transplantation LLT
    Population Age: Gender: Male, Female
    Trial protocol: BE (Completed)
    Trial results: View results
    EudraCT Number: 2009-012810-29 Sponsor Protocol Number: ALS-8-09-A-401 Start Date*: 2009-06-30
    Sponsor Name:Air Liquide Santé International
    Full Title: STABILITE HEMODYNAMIQUE LORS D’UNE ENDARTERIECTOMIE CAROTIDIENNE SOUS ANESTHESIE GENERALE CHEZ LE SUJET AGE : COMPARAISON LENOXe™ (xénon 100% v/v) versus SEVOFLURANE
    Medical condition: STABILITE HEMODYNAMIQUE LORS D’UNE ENDARTERIECTOMIE CAROTIDIENNE SOUS ANESTHESIE GENERALE CHEZ LE SUJET AGE : COMPARAISON LENOXe™ (xénon 100% v/v) versus SEVOFLURANE
    Disease:
    Population Age: Elderly Gender: Male, Female
    Trial protocol: FR (Ongoing)
    Trial results: (No results available)
    EudraCT Number: 2010-020677-17 Sponsor Protocol Number: ALMED-09-C3-026 Start Date*: 2011-11-16
    Sponsor Name:Air Liquide Santé International
    Full Title: Efficacy and safety of xenon anaesthesia compared to sevoflurane anaesthesia and total intravenous anaesthesia for on-pump coronary artery bypass graft surgery: a randomised, three-arm, single-blin...
    Medical condition: General anesthesia for on pump coronary artery bypass surgery
    Disease: Version SOC Term Classification Code Term Level
    14.1 10042613 - Surgical and medical procedures 10006894 CABG LLT
    Population Age: Adults, Elderly Gender: Male, Female
    Trial protocol: NL (Completed) DE (Completed)
    Trial results: View results
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    The status and protocol content of GB trials is no longer updated since 1 January 2021. For the UK, as of 31 January 2021, EU Law applies only to the territory of Northern Ireland (NI) to the extent foreseen in the Protocol on Ireland/NI. Legal notice
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