- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT00927017
The Effect of Liquorice on Plasma Potassium
April 6, 2010 updated by: University of Oulu
Lakritsin Vaikutus Kaliumpitoisuuteen
The hypothesis is that liquorice lowers plasma potassium.
This study aims to elucidate the dose-response of this effect with two doses of liquorice (66 grams or 102 grams) per day for two weeks.
Study Overview
Status
Terminated
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
9
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
-
Oulu, Finland, 90220
- Oulu University Hospital
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years to 40 years (Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
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
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Active Comparator: Liquorice 66 g/day
Liquorice given 66 grams per day for two weeks
|
Liquorice 66 g/day for two weeks
Other Names:
|
Active Comparator: Liquorice 102 g/day
Liquorice given 102 grams per day for two weeks
|
Liquorice 102 g/day for two weeks
Other Names:
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Change in plasma potassium
Time Frame: 1 week, 2 weeks
|
1 week, 2 weeks
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Janne Hukkanen, MD, PhD, Oulu University Hospital, Department of Internal Medicine
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
June 1, 2009
Primary Completion (Actual)
March 1, 2010
Study Completion (Actual)
March 1, 2010
Study Registration Dates
First Submitted
June 22, 2009
First Submitted That Met QC Criteria
June 23, 2009
First Posted (Estimate)
June 24, 2009
Study Record Updates
Last Update Posted (Estimate)
April 7, 2010
Last Update Submitted That Met QC Criteria
April 6, 2010
Last Verified
April 1, 2010
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- Lakritsi-2
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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