IRCT20130812014333N147
Recruiting
Phase 3
Comparative assessment of the efficacy and safety of addon treatment with Sofosbuvir-Daclatasvir”, Lithium”,and Trifluoprazine” to standard of care in three groups of patients with COVID-19
Overview
- Phase
- Phase 3
- Intervention
- Not specified
- Conditions
- Not specified
- Sponsor
- Kermanshah University of Medical Sciences
- Enrollment
- 80
- Status
- Recruiting
- Last Updated
- 5 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •Age over 18 years
- •Absolute lymphocyte count \<1100 / ML or SaO2 \<93
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 the treatment protocol to be followed easily
- •A history of known allergies to Sofosbuvir\-Velp, Trifluoprazine, Lithium and Trihexyphenidyl
- •Drugs that their concomitant use with standard treatment or Sofosbuvir\-Velpatasvir, Trifluoprazine, Lithium, and Trihexyphenidyl are contraindicated and can not be discontinued.
Outcomes
Primary Outcomes
Not specified
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