- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02649049
Dietary Determinants in Patients With Nonalcoholic Fatty Liver Disease (NAFLD)
September 21, 2016 updated by: Dr Azita Hekmatdoost, National Nutrition and Food Technology Institute
Assessment of Dietary Intakes of Patients With Nonalcoholic Fatty Liver Disease (NAFLD)
Patients with NAFLD and matched controls will be asked about their demographic status, and their previous year dietary intakes using a validated FFQ.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Observational
Enrollment (Actual)
1200
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
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-
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Tehran, Iran, Islamic Republic of, 19435
- NNFTRI clinic
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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 and older (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Probability Sample
Study Population
patients with NAFLD diagnosed using Fibroscan without any other chronic disorders.
Description
Inclusion Criteria:
- age more than 18
- NAFLD was diagnosed by Fibroscan and other hepatic disorders ruled out
Exclusion Criteria:
- not completing more than 10% of the questionnaire
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
- Observational Models: Case-Control
- Time Perspectives: Cross-Sectional
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
---|---|
Patients with NAFLD
Patients with NAFLD are the cases.
|
|
control group
Healthy people without NAFLD are controls.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
nonalcoholic fatty liver disease diagnosed by Fibroscan
Time Frame: 6 months
|
patients with confirmed diagnosis will be asked about their dietary intakes
|
6 months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
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
January 1, 2015
Primary Completion (Actual)
February 1, 2016
Study Completion (Actual)
March 1, 2016
Study Registration Dates
First Submitted
January 3, 2016
First Submitted That Met QC Criteria
January 5, 2016
First Posted (Estimate)
January 7, 2016
Study Record Updates
Last Update Posted (Estimate)
September 22, 2016
Last Update Submitted That Met QC Criteria
September 21, 2016
Last Verified
September 1, 2016
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 565
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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