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Clinical trials for Citicoline

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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    5 result(s) found for: Citicoline. Displaying page 1 of 1.
    EudraCT Number: 2005-004825-25 Sponsor Protocol Number: GF-ICTUS-04 Start Date*: 2006-05-30
    Sponsor Name:Ferrer Internacional
    Full Title: Citicoline in the treatment of acute ischemic stroke. An international randomized multicenter placebo-controlled study. Citicolina en el tratamiento del ictus isquémico agudo. Estudio internaciona...
    Medical condition: Acute ischemic stroke Ictus isquémico agudo
    Disease:
    Population Age: Adults, Elderly Gender: Male, Female
    Trial protocol: ES (Completed) PT (Completed) DE (Completed)
    Trial results: View results
    EudraCT Number: 2017-000762-29 Sponsor Protocol Number: COLAL/11/2016 Start Date*: 2017-10-09
    Sponsor Name:MDM S.P.A.
    Full Title: CHOLINA ALPHOSCERATE INJECTION VERSUS CITICOLINE INJECTION IN ELDERLY PATIENTS WITH COGNITIVE IMPAIRMENT RESULTING FROM CEREBROVASCULAR EVENT
    Medical condition: Cognitive impairment resulting from cerebrovascular event.
    Disease: Version SOC Term Classification Code Term Level
    21.1 100000004852 10009846 Cognitive impairment LLT
    21.1 100000004852 10000374 Accident cerebrovascular LLT
    Population Age: Elderly Gender: Male, Female
    Trial protocol: IT (Completed)
    Trial results: (No results available)
    EudraCT Number: 2014-005562-30 Sponsor Protocol Number: CITIPARK Start Date*: 2016-04-18
    Sponsor Name:PIAM FARMACEUTICI S.P.A.
    Full Title: Role of citicoline as supportive therapy in Parkinson’s disease.
    Medical condition: Parkinson's disease
    Disease: Version SOC Term Classification Code Term Level
    20.0 10029205 - Nervous system disorders 10029205 Nervous system disorders SOC
    Population Age: Adults, Elderly Gender: Male, Female
    Trial protocol: IT (Completed)
    Trial results: (No results available)
    EudraCT Number: 2006-006753-27 Sponsor Protocol Number: 129/2006/O/Sper Start Date*: 2007-01-23
    Sponsor Name:AZIENDA OSPEDALIERA DI BOLOGNA POLICLINICO S. ORSOLA M. MALPIGHI
    Full Title: Effects of oral CYTIDIN-5 -DIPHOSFOCHOLINE on vision function in the amblyopia
    Medical condition: Amblyopia
    Disease: Version SOC Term Classification Code Term Level
    9.1 10001906 Amblyopia LLT
    Population Age: Children, Under 18 Gender: Male, Female
    Trial protocol: IT (Completed)
    Trial results: View results
    EudraCT Number: 2009-017260-16 Sponsor Protocol Number: CAMELA Start Date*: 2010-11-05
    Sponsor Name:Consorci Mar Parc de salut de Barcelona (Parc de salut MAR)
    Full Title: CITICOLINA EN LA EVOLUCIÓN DE LA LEUCOARAIOSIS A MEDIO-LARGO PLAZO. ESTUDIO ALEATORIZADO Y CONTROLADO CON PLACEBO
    Medical condition: Leucoaraiosis
    Disease:
    Population Age: Elderly Gender: Male, Female
    Trial protocol: ES (Ongoing)
    Trial results: (No results available)
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    Query did not match any studies.
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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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