Skip to content

Efficacy of Levamisol in Treating COVID-19

Evaluation of Levamisole efficacy in treatment of COVID-19 and comparing it to the ?common treatment: a Clinical Trial

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20201124049480N1
Enrollment
365
Registered
2021-03-28
Start date
2021-04-21
Completion date
Unknown
Last updated
2021-11-01

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

Conditions

outpatient covid19 infected individuals. COVID-19

Interventions

Intervention 1: Intervention group: Levamisole 50 mg/day for ten days + routine management for covid19 based on national protocol (Hydroxychloroquine tablets 200 mg daily, acetaminophen 500 mg every 6

Sponsors

Artesh University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Age 18 years or older Positive RT PCR test for COVID-19 Full consent and acceptance of the patient or his companion for taking the drug Patient traceability Women should not become pregnant for 30 days after the end of the study patients should not take levamisole for five days before entering the study (because the half-life of ?the drug is 16 hours)

Exclusion criteria

Exclusion criteria: Another justifying cause (such as a bacterial or fungal infection) for the patient's symptoms Allergic reaction to levamisole Use of antibiotics other than those used to treat COVID-19 Shortness of breath due to cardiogenic pulmonary edema Lactation pregnancy Patients with unstable hemodynamics; History of cirrhosis, hepatitis, or severe liver disease, GFR ?less than 30 ml/min Patients receiving chemotherapy for cancer

Design outcomes

Primary

MeasureTime frame
The general condition of the patient. Timepoint: Days 1,3,5,7,9,14. Method of measurement: Verbal Numeric Scale(VNS).

Secondary

MeasureTime frame
Hospital admission. Timepoint: Day 1,3,5,7,9,14. Method of measurement: telephone.;Mortality rate. Timepoint: Day 1,3,5,7,9,14. Method of measurement: telephone.;Cough. Timepoint: Day 1,3,5,7,9,14. Method of measurement: telephone.;Sore throat. Timepoint: Day 1,3,5,7,9,14. Method of measurement: telephone.;Dyspnea. Timepoint: Day 1,3,5,7,9,14. Method of measurement: telephone.;Myalgia. Timepoint: Day 1,3,5,7,9,14. Method of measurement: telephone.;Diarrhea. Timepoint: Day 1,3,5,7,9,14. Method of measurement: telephone.;Vomiting. Timepoint: Day 1,3,5,7,9,14. Method of measurement: telephone.;Nausea. Timepoint: Day 1,3,5,7,9,14. Method of measurement: telephone.;Anosmia. Timepoint: Day 1,3,5,7,9,14. Method of measurement: telephone.;Dysgeusia. Timepoint: Day 1,3,5,7,9,14. Method of measurement: telephone.;Headache. Timepoint: Day 1,3,5,7,9,14. Method of measurement: telephone.;Fever. Timepoint: Day 1,3,5,7,9,14. Method of measurement: telephone.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMohammad Aminianfar

Artesh University of Medical Sciences

maminianfar@yahoo.com+98 21 4382 2449

Outcome results

None listed

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