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Impact of Sustained Virologic Response on Glycemic Control Among Diabetic Patients With Hepatitis C Virus Related Liver Disease

Impact of Sustained Virologic Response on Glycemic Control Among Diabetic Patients With Hepatitis C Virus Related Liver Disease

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03591783
Enrollment
140
Registered
2018-07-19
Start date
2018-08-31
Completion date
2019-12-31
Last updated
2018-07-19

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hepatitis c

Brief summary

Hepatitis C virus (HCV) is a major cause of chronic liver disease. The World Health Organization has reported that 170 million people are chronically infected with HCV globally. The highest prevalence of HCV infection worldwide exists in Egypt (15%); 90% of infection among Egyptian patients is due to genotype 4

Interventions

None listed

Sponsors

Assiut University
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

* Chronic HCV infection will be diagnosed based on positive testing for serum HCV RNA and anti-HCV Ab. * Diagnosis of type 2 DM will depend on fasting level of serum glucose more than 126 mg/dl and/or serum level of HbA1c more than 6.5 % on oral hypoglycemic therapy.

Exclusion criteria

* Chronic hepatitis due to causes other than HCV infection * Coinfection with HBV infection * Hepatocellular carcinoma * Child C stage of liver cirrhosis. * Patients with type I diabetes mellitus. * Cardiopulmonary diseases. * Major illness. * Patient receiving corticosteroids. * Patient refused consent.

Design outcomes

Primary

MeasureTime frameDescription
the percentage of patients with glycemic control3 monthsExploring the impact of achieving SVR by directly acting antiviral drugs on glycemic control among diabetic patients with HCV infection.

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026