A Clinical Trial Depicting Factors Associated with NAFLD and their effect on Severity of NAFLD

Not yet recruiting

• Conditions: Fatty (change of) liver, not elsewhere classified,

• Registration Number: CTRI/2023/05/052714
• Lead Sponsor: Dr Ansh Chaudhary

Brief Summary

This study is an observational cross sectional study, to study severity of vit B12 deficiency  , to evaluate thyroid dysfunction and to find diagnostic accuracies of AST/ALT Ratio, APRI, FIB4 scoring systems for predicting severity of NAFLD in 100 patients admitted in ward of Kasturba Hospital, Manipal and fitting into the inclusion and exclusion criteria.

Detailed Description

Not available

Study Timeline

• Study Start: 2023-01-07

Recruitment & Eligibility

• Status: Not Yet Recruiting
• Sex: All
• Target Recruitment: 100

Inclusion Criteria

1)Age more than 18 Years 2)All patients diagnosed as fatty liver by abdominal ultrasonography.

Exclusion Criteria

• 1)chronic liver diseases, including hepatitis B or C 2)alcoholic liver disease.
• 3)Patients on hepatotoxic medications.
• 4)Advanced liver disease 5)Cardiac failure 6)Acute fatty liver of pregnancy 7)Patients known case of Autoimmune Hepatitis 8)Any known Malignancy 9)Patients not giving consent.

Study & Design

• Study Type: Observational
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
1) Occurrence Of Vit B12 Deficiency In NAFLD	1.5 years
2) Occurrence of Thyroid Abnormalities in NAFLD	1.5 years
3) Diagnostic Accuracies of Predictive scoring systems in NAFLD	1.5 years

Secondary Outcome Measures

Name	Time	Method
1) Occurrence Of Vit B12 Deficiency In NAFLD	2) Occurrence of Thyroid Abnormalities in NAFLD

Trial Locations

Locations (1)

Kasturba Hospital; 🇮🇳 Udupi, KARNATAKA, India

Kasturba Hospital

🇮🇳Udupi, KARNATAKA, India

Dr Ansh Chaudhary

Principal investigator

8171370149

ansh2697@gmail.com