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Clinical trials for Carbocisteine

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   44341   clinical trials with a EudraCT protocol, of which   7370   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 ).  
     
    Examples: Cancer AND drug name. Pneumonia AND sponsor name.
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    Query did not match any clinical trials.
    These are paediatric studies completed by 26 January 2007, in respect of products authorised in the Community (Article 45 of the Paediatric Regulation (EC) No 1901/2006).
    Note: Advanced search filters for country, trial phase, gender, rare disease, IMP with orphan designation in the indication and age ranges of in-utero, adult or elderly do not apply to these records.
    Study title: Etude de l'efficacité et de la tolérance du carbocisteinate sachet versus carbocisteine sirop adulte dans un service de pneumologie. - Blanchon F. Brossel S- 10/10/1986.
    Active substance: CARBOCYSTEINE
    Study summary document link (including results):
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    Document reference: 23296
    Study title: Etude de l'efficacité et de la tolérance du carbocisteinate sachet versus carbocisteine sirop adulte dans un service de pneumologie. - Blanchon F. Brossel S- 10/10/1986.
    Active substance: CARBOCYSTEINE
    Study summary document link (including results):
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    Document reference: 23320
    Study title: Hypersensitivity reaction to acetylcysteine and carbocisteine. - No author - 1999 (Therapie, 54 (2):295) - Reference 87 updated dossier 2001 Sugar free formulation -
    Active substance: CARBOCYSTEINE
    Study summary document link (including results):
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    Document reference: 23288
    Study title: Intéret d'un mucolytique, la carbocisteine, dans la bronchite aigue de l'enfant - Malka M, Lablache Combier B - 1990 - La medecine Infantile, n. 8, 687-692
    Active substance: CARBOCYSTEINE
    Study summary document link (including results):
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    Document reference: 23259
    Study title: Modifications in nasal mucosa secretory iga levels during treatment of upper respiratory infections in the infants with carbocisteine.
    Active substance: CARBOCYSTEINE
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    Document reference: 23276
    Study title: Protection of respiratory mucosa by carbocisteine in children with recurrent infections.
    Active substance: CARBOCYSTEINE
    Study summary document link (including results):
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    Document reference: 23272
    Study title: Carbocisteine in the treatment of acute bronchitis in children.
    Active substance: CARBOCYSTEINE
    Study summary document link (including results):
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    Document reference: 23254
    Study title: Carbocisteine. - Brown D.T. et al. - 1988 (Drug Intell. Clin. Pharma., 22:603-8) - Reference 12 updated dossier 2001 Sugar free formulation -
    Active substance: CARBOCYSTEINE
    Study summary document link (including results):
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    Document reference: 23322
    Study title: Effect of carbocisteine on mucous and respiratory mucosa in children with recurrent bronchitis
    Active substance: CARBOCYSTEINE
    Study summary document link (including results):
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    Document reference: 23273
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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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