Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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TERMINATED
NA
9 participants
INTERVENTIONAL
2009-06-30
2010-03-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
NONE
Study Groups
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Liquorice 66 g/day
Liquorice given 66 grams per day for two weeks
Liquorice 66 g/day
Liquorice 66 g/day for two weeks
Liquorice 102 g/day
Liquorice given 102 grams per day for two weeks
Liquorice 102 g/day
Liquorice 102 g/day for two weeks
Interventions
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Liquorice 66 g/day
Liquorice 66 g/day for two weeks
Liquorice 102 g/day
Liquorice 102 g/day for two weeks
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
* age 18-40
Exclusion Criteria
* hypertension or hypotension
* allergy to liquorice
* pregnancy or lactation
* difficult venipuncture
* drug or alcohol abuse
* participation in pharmaceutical trial
18 Years
40 Years
ALL
Yes
Sponsors
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University of Oulu
OTHER
Responsible Party
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Oulu University Hospital, Department of Internal Medicine
Principal Investigators
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Janne Hukkanen, MD, PhD
Role: PRINCIPAL_INVESTIGATOR
Oulu University Hospital, Department of Internal Medicine
Locations
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Oulu University Hospital
Oulu, , Finland
Countries
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Other Identifiers
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Lakritsi-2
Identifier Type: -
Identifier Source: org_study_id
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