- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05106049
Serum Adiponectin as an Early Marker for Renal Impairment in Patients With Non-alcoholic Fatty Liver Disease.
October 23, 2021 updated by: Hend Abdelrheem Ahmed, Assiut University
Early Detection of Renal Impairment in Patients With Non-alcoholic Fatty Liver Disease by Measuring Serum Adiponectin Level.
Early detection of renal impairment in patients with non-alcoholic fatty liver disease and its correlation with serum Adiponectin level.
Study Overview
Status
Not yet recruiting
Conditions
Intervention / Treatment
Detailed Description
Detection of serum Adiponectin by ELISA technique using (EIA-3418) KIT, DRG international inc., USA
Study Type
Observational
Enrollment (Anticipated)
90
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Hend Abdelrheem, Resident
- Phone Number: 01011062442
- Email: hendabdelrheem@gmail.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 60 years (Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
cases are Non-alcoholic fatty liver patients who do not having any other health problem.
control group is healthy individuals.
Description
Inclusion Criteria:
- Patients with fatty liver aged from 18 to 60 yrs either diabetic or not .
- Patient with normal echogenic kidney in ultrasound and eGFR more than 60 mL/min/1.73m2.
- The Control group are completely healthy subjects without any systemic or liver and kidney affection
Exclusion Criteria:
- Patients less than 18 yrs & more than 60 yrs .
- All patients having any other causes of renal and hepatic disease rather than Diabetes and having any other systemic problem.
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: Retrospective
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
cases
non-alcoholic fatty liver patients
|
serum adiponectin as early marker for renal impairment.
Adiponectin is a recently identified adipose tissue-derived protein (adipocytokine) with important metabolic ,antiinflammatory, anti-atherogenic, and reactive oxygen species protective actions.
|
|
control
healthy persons
|
serum adiponectin as early marker for renal impairment.
Adiponectin is a recently identified adipose tissue-derived protein (adipocytokine) with important metabolic ,antiinflammatory, anti-atherogenic, and reactive oxygen species protective actions.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Correlate serum Adiponectin level with renal impairment in non-alcoholic fatty liver disease.
Time Frame: baseline
|
measure level of serum Adiponectin in non-alcoholic fatty liver patients to detect early renal impairment.
|
baseline
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Study Director: Mohamed Hassan, Profissor.as, Assiut University
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the 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 (Anticipated)
December 1, 2021
Primary Completion (Anticipated)
December 1, 2022
Study Completion (Anticipated)
January 1, 2023
Study Registration Dates
First Submitted
October 23, 2021
First Submitted That Met QC Criteria
October 23, 2021
First Posted (Actual)
November 3, 2021
Study Record Updates
Last Update Posted (Actual)
November 3, 2021
Last Update Submitted That Met QC Criteria
October 23, 2021
Last Verified
October 1, 2021
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- Adiponectin in NAFLD
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
No
Study Data/Documents
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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