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Efficacy of Daclatasvir and Sofosbuvir (Sovodak) in patients with HCV

Efficacy of Daclatasvir and Sofosbuvir (Sovodak) with Ribavirin and without Ribavirin in cirrhosis and non cirrhosis patients with HCV in Gastrointestinal and Liver Disease Research Center in 2017

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20080901001155N30
Enrollment
16
Registered
2018-10-24
Start date
2017-11-04
Completion date
Unknown
Last updated
2019-01-14

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

Conditions

Hepatitis C. Chapter I Certain infectious and parasitic diseases,Viral hepatitis (B15-B19)

Interventions

Intervention 1: Intervention group: 1.intervention group is cirrhosis patients with hepatitis C that would take 12 weeks of Sofosbovir 400 mg and Daclatasvir 60 mg (Sovodak) 1 pill made by Abidi plus

Sponsors

Rasht University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
35 Years to 75 Years

Inclusion criteria

Inclusion criteria: Patients who have not been treated before Patients who had been treated before, but their illness recurred Patients who could not take interferon

Exclusion criteria

Exclusion criteria: Patients who did not use the medication completely Patients with severe drug side effects Patients who were reluctant to participate in the plan

Design outcomes

Primary

MeasureTime frame
HCV treatment. Timepoint: 12 weeks after the end of treatment. Method of measurement: HCV- RNA PCR.

Secondary

MeasureTime frame
Possible side effect. Timepoint: Weeks 0.2, 4, 8, 12 and response to treatment, 24 weeks after the end of drug use (SVR 24. Method of measurement: weeks 2, 12 and 24 weeks after the end of drug use with use of PCR and 4,8 with use of liver enzymes test.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr. Farahnaz Joukar

Rasht University of Medical Sciences

farajov@yahoo.com+98 13 3353 5116

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026