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Clinical trials for Zinc gluconate

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   44336   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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    4 result(s) found for: Zinc gluconate. Displaying page 1 of 1.
    EudraCT Number: 2019-000905-57 Sponsor Protocol Number: wilson12345 Start Date*: 2019-04-17
    Sponsor Name:The Department of Hepatology and Gastroenterology, Aarhus University Hospital
    Full Title: Efficacy of zinc on human gut copper uptake depending on zinc type and dose regimen quantified with 64CuCl2 PET/CT-scan
    Medical condition: Healthy volunteers (Wilson's disease)
    Disease: Version SOC Term Classification Code Term Level
    20.0 100000004850 10047988 Wilson's disease LLT
    Population Age: Adults Gender: Male, Female
    Trial protocol: DK (Completed)
    Trial results: View results
    EudraCT Number: 2013-001866-40 Sponsor Protocol Number: ParoZink01 Start Date*: 2014-12-16
    Sponsor Name:University Hospital Schleswig-Holstein, UKSH Campus Kiel
    Full Title: The effect of Zinc-D-gluconate on bleeding propensity of the periodontium in patients with chronic parodontitis - a randomised, placebo-controlled, double-blind interventional study
    Medical condition: Chronic paradontitis in adults with at least 16 own teeth
    Disease:
    Population Age: Adults, Elderly Gender: Male, Female
    Trial protocol: DE (Completed)
    Trial results: (No results available)
    EudraCT Number: 2005-004641-34 Sponsor Protocol Number: RM-0205 Start Date*: 2006-02-07
    Sponsor Name:Matrixx Initiatives Inc
    Full Title: Human Clinical Study: Assessment of Zicam Cold Remedy RapidMelts
    Medical condition: to shorten the duration, reduce the number and decrease the sevity of common cold symptoms in otherwise healthy human adult volunteers
    Disease:
    Population Age: Adults Gender: Male, Female
    Trial protocol: GB (GB - no longer in EU/EEA)
    Trial results: (No results available)
    EudraCT Number: 2006-005405-67 Sponsor Protocol Number: 200602235 Start Date*: 2007-03-29
    Sponsor Name:LABCATAL [...]
    1. LABCATAL
    2. LABCATAL
    Full Title: Etude de l'efficacité et de la tolérance du L35 versus placebo dans le traitement de l'hidradénite suppurée (Maladie de Verneuil)
    Medical condition: Hidradénite suppurée (Maladie de Verneuil)
    Disease: Version SOC Term Classification Code Term Level
    9.1 10020041 Hidradenitis suppurativa LLT
    Population Age: Adults Gender: Male, Female
    Trial protocol: FR (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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