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Expression of Inflammasomes in HCV Patients

Expression of Inflammasomes in HCV Patients Before and After Treatment

Status
UNKNOWN
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04244383
Acronym
Inflammasome
Enrollment
50
Registered
2020-01-28
Start date
2020-01-31
Completion date
2020-07-31
Last updated
2020-01-28

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 has been identified a quarter of a decade ago as a leading cause of chronic viral hepatitis that can lead to cirrhosis and hepatocellular carcinoma. Only a minority of patients can clear the virus spontaneously during acute infection. Elimination of HCV during acute infection correlates with a rapid induction of innate and a delayed induction of adaptive immune responses. The majority of patients is unable to clear the virus and develops viral persistence despite the ongoing innate and adaptive immune response. The virus usually develops several strategies to escape these immune responses.

Interventions

DIAGNOSTIC_TESTinterleukin IL-1beta and interleukin IL-18

pro-inflammatory cytokines measured in the serum

Sponsors

Assiut University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
FACTORIAL
Primary purpose
OTHER
Masking
NONE

Intervention model description

chronic hepatitis C virus patients

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Chronic hepatitis C virus patients. * Patients do not start treatment protocol.

Exclusion criteria

* Pregnant women. * Hepato-cellular carcinoma patients. * Autoimmune disease patients. * Patients with liver cirrhosis. * Patients who refuse to participate in the study

Design outcomes

Primary

MeasureTime frameDescription
changes in the exprssion level of inflammasomes6 monthesobserve the changes in the exprssion level of inflammasomes in the selected chronic HCV patients before treatment with Sofosbuvir 400 mg and Daclatasvir 60 mg daily for 12 weeks and after sustained virological response at 12 weeks following the end of treatment (SVR12).

Contacts

Primary ContactKhaled Mohammed Hassanein, professor
khaledhassanein70@yahoo.com01118508060
Backup ContactHelal Foad Hetta, lecturer
helalhetta@yahoo.com0100311412

Outcome results

None listed

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