Prevalence of Non-alcoholic Fatty Liver Disease in Patients With Chronic Kidney Disease in Assiut

Sponsor
Muhammad Ameen Abdelrady Abdelaziz (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT06009250
Collaborator
(none)
200
12

Study Details

Study Description

Brief Summary

The goal of this observational study is to detect the prevalence of NAFLD in CKD patients

The main question[s] it aims to answer are:
  • [question 1] prevalence of NAFLD in CKD patients.

  • [question 2] the relationship between NAFLD and CKD.

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    The goal of this observational study is to detect the prevalence of NAFLD in CKD patients

    The main question[s] it aims to answer are:
    • [question 1] prevalence of NAFLD in CKD patients.

    • [question 2] the relationship between NAFLD and CKD.

    Study Design

    Study Type:
    Observational
    Anticipated Enrollment :
    200 participants
    Observational Model:
    Case-Control
    Time Perspective:
    Retrospective
    Official Title:
    Prevalence of Non-alcoholic Fatty Liver Disease in Patients With Chronic Kidney Disease in Assiut
    Anticipated Study Start Date :
    Dec 1, 2023
    Anticipated Primary Completion Date :
    Dec 1, 2024
    Anticipated Study Completion Date :
    Dec 1, 2024

    Arms and Interventions

    Arm Intervention/Treatment
    CKD patients

    CKD patient who are not DM are investigated for the presence of NAFLD

    normal control group

    normal population are investigated to know the prevalence of NAFLD in contrast to patients with CKD.

    Outcome Measures

    Primary Outcome Measures

    1. abdominal ultrasound [1 year]

      assessment of Liver regarding fatty liver disease by Ultrasound.

    2. liver enzymes [1 year]

      participants will undergo assessment of liver enzymes (AST and ALT) and results will be reporeted in a table.

    3. Fibroscan [1 year]

      participants will undergo fibroscanning of the liver to assess NAFLD and results will be reported in a table.

    4. BUN, Cr level and estimated GFR [1 year]

      participants will be assessed regarding BUN, CR and estimated GFR to confirm and follow up CKD patients involved in the study.

    5. Lipid Profile [1 year]

      participants will be assessed regarding Cholesterol level, Triglycerides, HDL and LDL. results will be reported in a table

    6. Complete Blood Picture (WBCs, HB, Patelets [1 year]

      total leucocytic count Hemoglobin level and platelet count will be assessed in our patients and will be reported in a table

    7. serum Uric Acid [1 year]

      serum uric acid will be assessed and reported in our patients

    Secondary Outcome Measures

    1. Waist Circumference [1 year]

      waist circumference measurement.

    2. Body Mass Index [1 year]

      BMI will also be calculated.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years to 80 Years
    Sexes Eligible for Study:
    All
    Inclusion Criteria:
    • CKD patients
    Exclusion Criteria:
    • HCV and HBV Positive patients

    • Alcoholics

    • patient on Hemodialysis

    • patients with wilson disease

    • patients with alpha one antitrypsin deficiency

    Contacts and Locations

    Locations

    No locations specified.

    Sponsors and Collaborators

    • Muhammad Ameen Abdelrady Abdelaziz

    Investigators

    None specified.

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Muhammad Ameen Abdelrady Abdelaziz, Internal Medicine Resident, Assiut University
    ClinicalTrials.gov Identifier:
    NCT06009250
    Other Study ID Numbers:
    • NAFLD and CKD
    First Posted:
    Aug 24, 2023
    Last Update Posted:
    Aug 24, 2023
    Last Verified:
    Aug 1, 2023

    Study Results

    No Results Posted as of Aug 24, 2023