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The European Union Clinical Trials Register   allows you to search for protocol and results information on:
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    The EU Clinical Trials Register currently displays   44338   clinical trials with a EudraCT protocol, of which   7368   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).

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    Study title: LMD124245 - Belzarena SD. Nasal intubation in paediatric patients. Comparison between a combination of alfentanil and lidocaine versus succinylcholine [translation]. Revista Brasileira de Anestesiologia, 46 (5), p. 323-328, 1996.LMD124245 - Belzarena SD. Nasal intubation in paediatric patients. Comparison between a combination of alfentanil and lidocaine versus succinylcholine [translation]. Revista Brasileira de Anestesiologia, 46 (5), p. 323-328, 1996.

    Type of medicine: Medicines containing chemical active substances
    Therapeutic area: Anesthesia and Analgesia [E03]
    Brands: Please see report, Please see report, Please see report
    MAH holders: Please see report, Please see report, Please see report
    Assessment:
    Active substance: ALFENTANIL
    ATC code: N01AH02
    Document link: belzarenaengabstract_alfentanil.pdf
    Document date: 2011-11-22
    Study number:
    EudraCT number:
    Scope of study: Clinical
    Population of study subjects: Preterm newborn Infants Newborn infants (1 to 27 days) Infants and toddlers (28 days to 24 months) Children (2 to 11 years) Adolescents (12 to 18 years)
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    The status and protocol content of GB trials is no longer updated since 1 January 2021.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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