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Sofosbuvir and Daclatasvir for treatment of Hepatitis-C in patients undergoing hemodialysis.

Efficacy and tolerability of Sofosbuvir and Daclatasvir for treatment of Hepatitis C genotype 3 in patients undergoing hemodialysis- A Prospective interventional clinical trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20170614034526N3
Enrollment
36
Registered
2019-03-08
Start date
2017-08-01
Completion date
Unknown
Last updated
2019-03-25

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

Conditions

Condition 1: Chronic Viral Hepatitis-C. Condition 2: Chronic kidney disease, stage 5. Chronic viral hepatitis C Chronic kidney disease, stage 5

Interventions

Intervention 1: Intervention group 1: Daclatasvir 60 mg + Sofosbuvir 400 mg once daily for 12 weeks. Intervention 2: Intervention group 2: Daclatasvir 60 mg per day and Sofosbuvir 400 mg 3 times / per

Sponsors

Jinnah Hospital, Lahore
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Male & Female (non-pregnant) being at the age of 18 years and over End stage renal disease patients undergoing maintenance hemodialysis detected with HCV RNA by PCR.

Exclusion criteria

Exclusion criteria: Patients having co-infection with HBV, HIV. Patients with decompensated cirrhosis and terminal illness. Patients hypersensitive to any of the ingredients of treatment drugs.

Design outcomes

Primary

MeasureTime frame
Sustained Virologic Response (SVR) assessed. Timepoint: 24th week after start of treatment. Method of measurement: HCV RNA- PCR.

Secondary

MeasureTime frame
End of Treatment response (ETR). Timepoint: 12th week of start of treatment. Method of measurement: HCV RNA-PCR.

Countries

Pakistan

Contacts

Public ContactProf. Dr. Shafiq Ur Rehman Cheema

Jinnah Hospital & Allama Iqbal Medical College, Lahore

shafiqcheema@yahoo.com+92 42 99231400

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 20, 2026