- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02176811
Plasma Betatrophin Levels in Non-alcoholic Fatty Liver Disease
The Cross Sectional Study to Investigate the Plasma Betatrophin Levels in Non-alcoholic Fatty Liver Disease and Healthy Controls
The study searched for answers to two questions:
1-What are the plasma betatrophin levels in subjects with non-alcoholic fatty liver disease and healthy controls.
2. Is there any relationship between plasma betatropin levels and different stage of non-alcoholic fatty liver disease 2.Is there any relationship between plasma betatropin levels and metabolic parameters in subjects with non-alcoholic fatty liver disease.
Study Overview
Status
Conditions
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
-
-
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Ankara, Turkey, 06018
- Gulhane School of Medicine Department of Endocrinology and Metabolism
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- Patients with biopsy proven non-alcoholic fatty liver disease
Exclusion Criteria:
- Taking any drugs
- >20 gr/day alcohol consumption
- chronic metabolic diseases
- morbid obesity
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
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Non-alcoholic Fatty Liver Disese
no treatment
|
healthy controls
no treatment
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Plasma betatrophin levels in subjects with non-alcoholic fatty liver disease and healthy controls.
Time Frame: 6 months
|
6 months
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- GSM-052014
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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