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Main
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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register. |
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Register:
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ClinicalTrials.gov |
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Last refreshed on:
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19 February 2015 |
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Main ID: |
NCT00927017 |
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Date of registration:
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22/06/2009 |
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Prospective Registration:
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No |
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Primary sponsor: |
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Public title:
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The Effect of Liquorice on Plasma Potassium
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Scientific title:
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Lakritsin Vaikutus Kaliumpitoisuuteen |
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Date of first enrolment:
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June 2009 |
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Target sample size:
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9 |
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Recruitment status: |
Terminated |
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URL:
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http://clinicaltrials.gov/show/NCT00927017 |
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Study type:
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Interventional |
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Study design:
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Allocation: Randomized, Endpoint Classification: Safety Study, Intervention Model: Parallel Assignment, Masking: Open Label
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Phase:
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N/A
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Countries of recruitment
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Finland
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Contacts
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Name:
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Janne Hukkanen, MD, PhD |
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Address:
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Telephone:
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Email:
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Affiliation:
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Oulu University Hospital, Department of Internal Medicine |
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Key inclusion & exclusion criteria
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Inclusion Criteria:
- healthy volunteers
- age 18-40
Exclusion Criteria:
- any continuous medication
- hypertension or hypotension
- allergy to liquorice
- pregnancy or lactation
- difficult venipuncture
- drug or alcohol abuse
- participation in pharmaceutical trial
Age minimum:
18 Years
Age maximum:
40 Years
Gender:
Both
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Health Condition(s) or Problem(s) studied
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Healthy
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Intervention(s)
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Other: Liquorice 66 g/day
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Other: Liquorice 102 g/day
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Primary Outcome(s)
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Change in plasma potassium
[Time Frame: 1 week, 2 weeks]
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Secondary ID(s)
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Lakritsi-2
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Source(s) of Monetary Support
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Please refer to primary and secondary sponsors
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Results
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Results available:
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Date Posted:
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Date Completed:
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URL:
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