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Clinical trials for Cisatracurium

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   44334   clinical trials with a EudraCT protocol, of which   7366   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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    9 result(s) found for: Cisatracurium. Displaying page 1 of 1.
    EudraCT Number: 2013-000721-31 Sponsor Protocol Number: MONITOR Start Date*: 2013-05-07
    Sponsor Name:CHU DE POITIERS
    Full Title: Comparison of neuromuscular blockade’s monitoring and clinical assessment during cisatracurium paralysis in critically ill patients
    Medical condition: To be able to perform an efficient neuromuscular blockade with the lowest dose of cisatracurium in mechanically ventilated critically ill patients. The neuromuscular blockade is assessed by TOF mon...
    Disease:
    Population Age: Adults, Elderly Gender: Male, Female
    Trial protocol: FR (Ongoing)
    Trial results: (No results available)
    EudraCT Number: 2009-017921-20 Sponsor Protocol Number: none Start Date*: 2010-09-16
    Sponsor Name:Univ. Klinik für Anästhesiologie
    Full Title: Influence of Gender on the Plasma-Effect site equilibration time of propofol anesthetic and Cisatracurium Besylate neuromuscular blocking agent. A pilot study.
    Medical condition: effect of Gender on Pharmacokinetics of Propofol and cisatracurium
    Disease:
    Population Age: Adults Gender: Male, Female
    Trial protocol: AT (Completed)
    Trial results: View results
    EudraCT Number: 2014-004951-30 Sponsor Protocol Number: RBHP_2014_KAUFFMANN Start Date*: 2015-01-20
    Sponsor Name:CHU de Clermont-Ferrand
    Full Title:
    Medical condition:
    Disease:
    Population Age: Adults, Elderly Gender: Male, Female
    Trial protocol: FR (Ongoing)
    Trial results: (No results available)
    EudraCT Number: 2005-001622-91 Sponsor Protocol Number: RKMMS 04 Start Date*: 2005-06-23
    Sponsor Name:Royal Group Hospitals
    Full Title: A randomised assessor blinded study to examine the role of skin testing in the prediction of peri-operative anaphylaxis and its correlation with mast cell tryptase and total IgE.
    Medical condition: Prevalance of sensitivity of immune system to the four named neuromuscular blocking drugs in patients undergoing anaesthesia.
    Disease:
    Population Age: Adults, Elderly Gender: Male, Female
    Trial protocol: GB (GB - no longer in EU/EEA)
    Trial results: (No results available)
    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.
    Disease: Version SOC Term Classification Code Term Level
    8.1 10002091 Anaesthesia PT
    Population Age: Adults, Elderly Gender: Male, Female
    Trial protocol: FI (Completed)
    Trial results: View results
    EudraCT Number: 2008-001236-13 Sponsor Protocol Number: 2008-001236-13 Start Date*: 2007-12-01
    Sponsor Name:AZIENDA OSPEDALIERA DI PADOVA
    Full Title: Sperimental controlled and randomized in singol blind study. Use of continuous epidural ketamina in patients submitted to toracotomy for pulmonary resection.
    Medical condition: pulmonary resection
    Disease: Version SOC Term Classification Code Term Level
    9.1 10038738 SOC
    Population Age: Adults, Elderly Gender: Male, Female
    Trial protocol: IT (Ongoing)
    Trial results: (No results available)
    EudraCT Number: 2015-003055-22 Sponsor Protocol Number: AOL2015-04 Start Date*: 2016-05-09
    Sponsor Name:Centre Hospitalier Universitaire de Reims
    Full Title: Intérêt de la curarisation lors de la chirurgie laparoscopique et recherche de facteurs associés à une compliance abdominale diminuée.
    Medical condition: patients pris en charge pour une chirurgie intra-péritonéale programmée par laparoscopie
    Disease:
    Population Age: Adults Gender: Male, Female
    Trial protocol: FR (Ongoing)
    Trial results: (No results available)
    EudraCT Number: 2005-001792-35 Sponsor Protocol Number: 19.4.310 Start Date*: 2005-09-28
    Sponsor Name:NV Organon
    Full Title: Comparison of rocuronium and Org 25969 with cis-atracurium and neostigmine when neuromuscular block is reversed at reappearance of T2
    Medical condition: Not applicable
    Disease:
    Population Age: Adults, Elderly Gender: Male, Female
    Trial protocol: GB (Completed) IT (Completed)
    Trial results: View results
    EudraCT Number: 2013-004423-36 Sponsor Protocol Number: MK-8616-104 Start Date*: 2015-01-12
    Sponsor Name:MSD Italia s.r.l.
    Full Title: Randomized, parallel group, controlled trial to compare two different “NMB + reversal” strategies in adult obese patients underwent laparoscopic abdominal surgery (Phase 4; Protocol No. MK-8616-104...
    Medical condition: Obese adults to be subjected to abdominal laparoscopic surgery
    Disease:
    Population Age: Adults Gender: Male, Female
    Trial protocol: IT (Prematurely Ended)
    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
    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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