Clinical Trials Directory

Trials / Completed

CompletedNCT03188276

The Relationship Between MDSCs and NK Cells Activity of CHC Patient Treated by DAAs

The Relationship Between Direct Acting Antiviral Treatment Effect and Myeloid-Derived Suppressor Cells and NK Cells Activity in Chronic Hepatitis C

Status
Completed
Phase
EARLY_Phase 1
Study type
Interventional
Enrollment
52 (actual)
Sponsor
Third Affiliated Hospital, Sun Yat-Sen University · Academic / Other
Sex
All
Age
18 Years – 76 Years
Healthy volunteers
Accepted

Summary

Hepatitis C virus (HCV) infection is easy to chronic and can progress to cirrhosis and liver cancer. Direct-acting antiviral treatment can significantly improve the prognosis of the disease and the efficacy is seemingly not affected by a variety of viral factors. In addition, direct-acting antiviral agents therapy may affect the transformation of the immune cells and ameliorate the host immune status consequently. This study mainly investigated the relationship between Direct Acting Antiviral Treatment effect and the functional activity of myeloid-derived suppressor cells (MDSCs) and natural killer cells (NK cells) in Chronic Hepatitis C.

Detailed description

32 treatment-naive CHC patients and 20 healthy controls were recruited. Patients were examined before DAAs therapy (0w) and at weeks 4 (4w) and weeks 12 (12w) and weeks24 (24w) of the therapy. The percent age of myeloid-derived suppressor cells and NK cells of the peripheral blood were analyzed by flow cytometry. The investigators discuss the relationship between direct acting antiviral treatment effect and myeloid-derived suppressor cells and NK cells activity in chronic hepatitis C.

Conditions

Interventions

TypeNameDescription
DRUGLedipasvir-Sofosbuvir15 CHC patients were treated with Sofosbuvir (400mg, qd)/Ledipasvir (90mg, qd) for 12 weeks
DRUGDaclatasvir-Sofosbuvir17 CHC patients were treated with Sofosbuvir (400mg, qd)/Daclatasvir (60mg,qd) for 12 weeks.

Timeline

Start date
2016-02-01
Primary completion
2017-05-01
Completion
2017-05-01
First posted
2017-06-15
Last updated
2017-06-15

Source: ClinicalTrials.gov record NCT03188276. Inclusion in this directory is not an endorsement.