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Clinical trials for Thiopental

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
  • clinical trials conducted outside the EU/EEA that are linked to European paediatric-medicine development

    • 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   44364   clinical trials with a EudraCT protocol, of which   7388   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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    6 result(s) found for: Thiopental. Displaying page 1 of 1.
    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.
    Disease: Version SOC Term Classification Code Term Level
    21.1 100000004865 10018061 General anesthesia LLT
    Population Age: Preterm newborn infants, Newborns, Under 18 Gender: Male, Female
    Trial protocol: DK (Trial now transitioned)
    Trial results: (No results available)
    EudraCT Number: 2009-015584-13 Sponsor Protocol Number: 1A-AGE/ONSET Start Date*: 2009-10-20
    Sponsor Name:Rigshospitalet
    Full Title: Onset-tid samt hæmodynamisk respons på anæstesi indledning hos ældre ved sammenligning af thiopental og propofol
    Medical condition: Induction of anaesthesia in an elderly population
    Disease: Version SOC Term Classification Code Term Level
    12.0 10021724 Induction of anaesthesia LLT
    Population Age: Adults, Elderly Gender: Male, Female
    Trial protocol: DK (Completed)
    Trial results: View results
    EudraCT Number: 2008-002690-12 Sponsor Protocol Number: 2008-209 Start Date*: 2008-08-19
    Sponsor Name:Glostrup Hospital
    Full Title: Sammenligning af to forskellige bedøvelser af børn til MR-scanning. Fordele, ulemper og tidsforbrug ved de to metoder.
    Medical condition: Børn, der skal have foretaget MR scanning i generel anæstesi.
    Disease:
    Population Age: Infants and toddlers, Children, Under 18 Gender: Male, Female
    Trial protocol: DK (Completed)
    Trial results: (No results available)
    EudraCT Number: 2008-004979-21 Sponsor Protocol Number: 0816 Start Date*: 2008-10-23
    Sponsor Name:CHU de Grenoble
    Full Title: Effet comparé de deux doses de Mannitol sur l'hypertension intracrânienne.
    Medical condition: Hypertension intracrânienne post traumatique
    Disease:
    Population Age: Adults, Elderly Gender: Male, Female
    Trial protocol: FR (Ongoing)
    Trial results: (No results available)
    EudraCT Number: 2004-001782-18 Sponsor Protocol Number: MRZ 92579-0404/1 Start Date*: 2005-02-14
    Sponsor Name:Merz Pharmaceuticals GmbH
    Full Title: Saftey and efficacy of two different doses of Neramexane mesylate as preemptive analgesic and add-on therapy to opioids in the management of postoperative pain. A randomised, double-blind, placebo-...
    Medical condition: Moderate to severe acute postoperative pain
    Disease: Version SOC Term Classification Code Term Level
    7.1 10054711 LLT
    Population Age: Adults, Elderly Gender: Male, Female
    Trial protocol: CZ (Completed)
    Trial results: View results
    EudraCT Number: 2009-013201-33 Sponsor Protocol Number: fMRIPed1 Start Date*: 2009-09-30
    Sponsor Name:FONDAZIONE CENTRO S. RAFFAELE DEL MONTE TABOR
    Full Title: Propofol and Tiopentone in paediatric sedation for fRMI study.
    Medical condition: chirldren aged from 1 to 4 years old undergoing fMRI for convulsive crisis or delay in growth
    Disease: Version SOC Term Classification Code Term Level
    12.0 10010914 Convulsions LLT
    Population Age: Children, Under 18 Gender: Male, Female
    Trial protocol: IT (Completed)
    Trial results: (No results available)
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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
    As of 31 January 2023, all EU/EEA initial clinical trial applications must be submitted through CTIS . Updated EudraCT trials information and information on PIP/Art 46 trials conducted exclusively in third countries continues to be submitted through EudraCT and published on this website.

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