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Comparative assessment of the efficacy and safety of add ontreatment with “Sofosbuvir standard of care therapeutic regimenVelpatasvir” to “standard of caretherapeutic regimen” in patients with COVID-19

Comparative assessment of the efficacy and safety of add ontreatment with “Sofosbuvir plus Velpatasvir” to “standard of care therapeutic regimen” in patients with COVID-19

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20130812014333N145
Enrollment
80
Registered
2020-03-30
Start date
2020-04-08
Completion date
Unknown
Last updated
2020-05-18

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

Conditions

COVID-19. COVID-19 disease

Interventions

Intervention 1: The intervention group in addition to standard treatment (400 mg of hydroxychloroquine and 100 to 400 mg of Lupinavir-ritonavir at a time), will receive 100 to 400 mg of Sofosbuvir-Ve

Sponsors

Kermanshah University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Age over 18 years Absolute lymphocyte count <1100 / ML or SaO2 <93

Exclusion criteria

Exclusion criteria: Pregnancy or breast-feeding The physician's decision that the trial is not in the patient's interest Any circumstances that do not allow to follow the treatment protocol easily A history of severe liver disease including cirrhosis or ALT or AST levels more than fives times normal Drugs that are contraindicated with standard treatment or Sofosbuvir-Velpatasvir and cannot be discontinued History of untreated HIV infection or hepatitis C

Design outcomes

Primary

MeasureTime frame
Clinical status. Timepoint: Beginning of the study, 10 days later, or discharge time. Method of measurement: By a doctor.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr. Reza Khodarahmi

Kermanshah University of Medical Sciences

rkhodarahmi@mbrc.ac.ir+98 83 3426 6780

Outcome results

None listed

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