- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03172650
Effect of Non-alcoholic Fatty Liver Disease on Kidney Functions
August 13, 2017 updated by: Ahmed Mohamed Abbas, Assiut University
Effect of Non-alcoholic Fatty Liver Disease on Kidney Functions: Observational Case Control Study in Upper Egypt
Non-alcoholic fatty liver disease is the most common cause of chronic liver disease worldwide.
It is defined as the accumulation of fat (>5%) in the liver cells in the absence of excessive alcohol intake or other causes of liver disease including viral, drug-induced, or autoimmune.
Non-alcoholic fatty liver disease is a hepatic manifestation of metabolic syndrome.
Study Overview
Status
Unknown
Conditions
Intervention / Treatment
Study Type
Observational
Enrollment (Anticipated)
120
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
-
-
Cairo
-
Assiut, Cairo, Egypt, 002
- Recruiting
- Ahmed Abbas
-
Contact:
- Ahmed Abbas
-
Contact:
- ahmed abbas, MD
- Email: bmr90@hotmail.com
-
-
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 70 years (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Probability Sample
Study Population
Patients will be recruited outpatient clinic of internal medicine of Luxor international hospital and Assiut university hospital
Description
Inclusion criteria:
- All non alcoholic fatty liver disease patients evidenced by abdominal ultrasound.
- Urine analysis whether normal or renal sedimentation.
Exclusion criteria:
- Alcoholic fatty liver patients.
- patients known to have diabetes mellitus.
- patients with other causes of liver disease as viral hepatitis, drug induced,or autoimmune.
- patients known to have kidney disease.
- Hypertension.
- Hyperuricemia.
- Impaired urea and creatinine patients.
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
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
study group
non alcoholic fatty liver disease patients
|
collection of blood sample 5 milliliter for calculation of glomerular filtration rate
|
|
Control group
fatty liver patients
|
collection of blood sample 5 milliliter for calculation of glomerular filtration rate
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
The percentage of patients with abnormal laboratory glomerular filtration rate
Time Frame: 1 day
|
decreased glomerular filtration rate <60 mL/minute will be considered abnormal
|
1 day
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
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 (Actual)
July 1, 2017
Primary Completion (Anticipated)
July 1, 2018
Study Completion (Anticipated)
September 1, 2018
Study Registration Dates
First Submitted
May 30, 2017
First Submitted That Met QC Criteria
May 30, 2017
First Posted (Actual)
June 1, 2017
Study Record Updates
Last Update Posted (Actual)
August 16, 2017
Last Update Submitted That Met QC Criteria
August 13, 2017
Last Verified
August 1, 2017
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- NAFLD
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
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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