- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07168551
- Original Trial
Is There a Relationship Between Uric Acid Level and Liver Fibrosis in Obese Patients
Association of Hyperuricemia and Non Alcoholic Fatty Liver Disease and Liver Fibrosis Risk in Adult Obese Patients
- Identifying the association between hyperuricemia and NAFLD can lead to early detection and prevention of liver fibrosis in adult obese patients.
- Understanding the relationship between hyperuricemia and NAFLD can inform targeted therapy, such as urate-lowering treatment, to potentially slow disease progression.
3 - To examine the relationship between serum uric acid levels and liver fibrosis severity*: Assessing the correlation between serum uric acid levels and the severity of liver fibrosis in adult obese patients with NAFLD.
4- To identify potential mechanisms underlying the association*: Exploring the potential mechanisms by which hyperuricemia may contribute to the development and progression of NAFLD and liver fibrosis in adult obese patients.
Study Overview
Status
Intervention / Treatment
- Diagnostic test: *Lab Methods:* 1- Serum Uric Acid levels 2-Liver Function Tests 3- Lipid Profile . 4- Haemoglobin A1c level . 5- Serum glucose level .
- Radiation: *Imaging Studies:* 1- Ultrasound 2 - FibroScan
- Device: Instruments:* 1- *Automated Analyzers*: Used for blood tests, such as serum uric acid and liver function tests.
Detailed Description
Hyperuricemia is associated with nonalcoholic fatty liver disease (NAFLD), whereas whether the association differed by hyperuricemia onset age remained unclear. This study sought to investigate the associations of hyperuricemia onset age with the risk of incident NAFLD across adulthood.
Obesity has been demonstrated to show a consistent link with the increased possibility of nonalcoholic fatty liver disease (NAFLD). Since both serum uric acid (SUA) and obesity are essential components of metabolic syndrome (MetS), it is uncertain whether the incidence of NAFLD results from serum uric acid, obesity, or other potential factors based on previous studies.
Study Type
Enrollment (Estimated)
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- Age: Adults (typically 18-65 years old)
2 - Body Mass Index (BMI): Obese patients with a BMI ≥ 30 kg/m²
3- Hyperuricemia : Elevated serum uric acid levels (typically > 7 mg/dL for men and > 6 mg/dL for women)
Exclusion Criteria:
excessive alcohol consumption ( > 20 gm /day in men and 10 in g /day in women )
2- use of steatogenic within the past 6 months
3- positive test for hepatitis B surface antigen and hepatitis B core antibody
4- Drug induced liver injury and autoimmune hepatitis
5 - cirrhosis and other causes of liver disease
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
Healthy controls
|
Lab methods
Imaging
Instrument
|
|
1- obese +-nafld+- fibrosis
Obese patients with non alcoholic fatty liver disease with fibrosis
|
Lab methods
Imaging
Instrument
|
|
obese +- hyperuricemia +- nfld+- fibrosis
Obese patients with hyperuricemia and non alcoholic liver disease and fibrosis
|
Lab methods
Imaging
Instrument
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Prevalence of NAFLD
Time Frame: 1 year
|
The proportion of adult obese patients with NAFLD in the study population
|
1 year
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Serum uric acid level
Time Frame: 1 year
|
The serum uric acid level in adult obese patients
|
1 year
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Estimated)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimated)
Study Record Updates
Last Update Posted (Estimated)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
- Pathologic Processes
- Digestive System Diseases
- Liver Diseases
- Fibrosis
- Fatty Liver
- Pathological Conditions, Signs and Symptoms
- Hyperuricemia
- Non-alcoholic Fatty Liver Disease
- Liver Cirrhosis
- Investigative Techniques
- Clinical Laboratory Techniques
- Diagnostic Techniques and Procedures
- Diagnosis
- Diagnostic Techniques, Digestive System
- Hematologic Tests
- Liver Function Tests
Other Study ID Numbers
- UNLF
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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