NCT07168551

Brief Summary

  1. 1.Identifying the association between hyperuricemia and NAFLD can lead to early detection and prevention of liver fibrosis in adult obese patients.
  2. 2.Understanding the relationship between hyperuricemia and NAFLD can inform targeted therapy, such as urate-lowering treatment, to potentially slow disease progression.

Trial Health

65
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
111

participants targeted

Target at P50-P75 for all trials

Timeline
7mo left

Started Oct 2025

Status
not yet recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Progress51%
Oct 2025Dec 2026

First Submitted

Initial submission to the registry

August 27, 2025

Completed
15 days until next milestone

First Posted

Study publicly available on registry

September 11, 2025

Completed
20 days until next milestone

Study Start

First participant enrolled

October 1, 2025

Completed
1 year until next milestone

Primary Completion

Last participant's last visit for primary outcome

October 1, 2026

Expected
2 months until next milestone

Study Completion

Last participant's last visit for all outcomes

December 1, 2026

Last Updated

September 15, 2025

Status Verified

August 1, 2025

Enrollment Period

1 year

First QC Date

August 27, 2025

Last Update Submit

September 12, 2025

Conditions

Outcome Measures

Primary Outcomes (1)

  • Prevalence of NAFLD

    The proportion of adult obese patients with NAFLD in the study population

    1 year

Secondary Outcomes (1)

  • Serum uric acid level

    1 year

Study Arms (3)

1- obese +-nafld+- fibrosis

Obese patients with non alcoholic fatty liver disease with fibrosis

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 - FibroScanDevice: Instruments:* 1- *Automated Analyzers*: Used for blood tests, such as serum uric acid and liver function tests.

obese +- hyperuricemia +- nfld+- fibrosis

Obese patients with hyperuricemia and non alcoholic liver disease and fibrosis

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 - FibroScanDevice: Instruments:* 1- *Automated Analyzers*: Used for blood tests, such as serum uric acid and liver function tests.

Healthy controls

Healthy controls

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 - FibroScanDevice: Instruments:* 1- *Automated Analyzers*: Used for blood tests, such as serum uric acid and liver function tests.

Interventions

Lab methods

1- obese +-nafld+- fibrosisHealthy controlsobese +- hyperuricemia +- nfld+- fibrosis

Imaging

1- obese +-nafld+- fibrosisHealthy controlsobese +- hyperuricemia +- nfld+- fibrosis

Instrument

1- obese +-nafld+- fibrosisHealthy controlsobese +- hyperuricemia +- nfld+- fibrosis

Eligibility Criteria

Age18 Years - 65 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

Adult obese patients

You may qualify if:

  • Age: Adults (typically 18-65 years old)
  • Body Mass Index (BMI): Obese patients with a BMI ≥ 30 kg/m²
  • Hyperuricemia : Elevated serum uric acid levels (typically \> 7 mg/dL for men and \> 6 mg/dL for women)

You may not qualify if:

  • excessive alcohol consumption ( \> 20 gm /day in men and 10 in g /day in women )
  • use of steatogenic within the past 6 months
  • positive test for hepatitis B surface antigen and hepatitis B core antibody
  • Drug induced liver injury and autoimmune hepatitis
  • cirrhosis and other causes of liver disease

Contact the study team to confirm eligibility.

Sponsors & Collaborators

MeSH Terms

Conditions

HyperuricemiaNon-alcoholic Fatty Liver DiseaseLiver Cirrhosis

Interventions

Hematologic TestsLiver Function Tests

Condition Hierarchy (Ancestors)

Pathologic ProcessesPathological Conditions, Signs and SymptomsFatty LiverLiver DiseasesDigestive System DiseasesFibrosis

Intervention Hierarchy (Ancestors)

Clinical Laboratory TechniquesDiagnostic Techniques and ProceduresDiagnosisInvestigative TechniquesDiagnostic Techniques, Digestive System

Study Design

Study Type
observational
Observational Model
OTHER
Time Perspective
CROSS SECTIONAL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Internal medicine Resident doctor

Study Record Dates

First Submitted

August 27, 2025

First Posted

September 11, 2025

Study Start

October 1, 2025

Primary Completion (Estimated)

October 1, 2026

Study Completion (Estimated)

December 1, 2026

Last Updated

September 15, 2025

Record last verified: 2025-08