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Clinical Trials/NCT04331470
NCT04331470
Unknown
Phase 2

Evaluation of Efficacy of Pharmacotherapy Treatment of COVID- 19 Infection Using Oral Levamisole and Formoterol+Budesonide Inhaler and Comparison of This Treatment Protocol With Standard National Treatment of the Disease

Fasa University of Medical Sciences1 site in 1 country30 target enrollmentApril 4, 2020

Overview

Phase
Phase 2
Intervention
Levamisole Pill + Budesonide+Formoterol inhaler
Conditions
COVID-19
Sponsor
Fasa University of Medical Sciences
Enrollment
30
Locations
1
Primary Endpoint
Clear chest CT-scan
Last Updated
6 years ago

Overview

Brief Summary

New Corona virus (COVID-19) has made a horrible situation for all of the countries. This disease is not only a health problem but also economy, culture and the whole entity of the countries is under attack by the virus. This disease seems to affect the body in two different pathology pathways. From one side virus can decrease activity of immune system in the blood stream and whole body and from other side it can attack the respiratory cells. Tissue biopsy shows that immune cells penetrate into the Lung tissue and we have accumulation and over activity of Immune cells in the lung. This inflammation in respiratory tract probably is the major cause of Cytokine storm and release of TNF-α and IL-6 into the blood.

It seems that by three strategy disease can be treated. 1- By using systemic immune simulators. 2- By using topical anti-inflammatory drug in the respiratory system (Steroids or NSAIDs) 3- By inhibition of replication of the virus in the attacked cells.

Detailed Description

Looking at the pathology of this disease shows that COVID-19 virus binds to the Angiotensin converting enzyme II (ACE II) which is located on the surface of different cells in the body and specially on the cells of respiratory system. This enzyme is responsible to turn angiotensin II into angiotensin1-7. It is also turns angiotensin I into angiotensin 1-9. When ACEII would be blocked by virus level of angiotensin II will be increased and this enzyme along with vasoconstriction, makes cells to manufacture TNF α and IL-6 which are responsible for cytokine storm and Lymphopenia. Also presence of virus and virus shell on the surface of the infected cells make immune system to attack to the respiratory system hence effect of angiotensin II inside the cell causes fibrosis of the respiratory cells. This inflammation and tissue damage make Acute Respiratory Distress syndrome (ARDS) which is lethal for patients. There is a dilemma in treatment of this infection. From one side it doesn't make sense to decrease the immune response hence it will make the infection worse. And from other side stimulation of the immune response because of respiratory inflammation can expedite process of lethal ARDS. A new strategy for treatment of this disease which consists of local anti- inflammatory and systemic immune stimulant drugs can be considered as a reasonable strategy.As immunostimulator, Levamisole can increase Lymphocytes and empower the immunity of the body. This drug can also bind to Papaine Like Protease(PL-pro) of the shell of the virus which is necessary for virulence of COVID-19. It also can decrease level of TNF α and IL-6, and as a chemical adjutant can introduce the virus to the immune system. In addition to Levamisole, Formoterol+Budesonide inhaler can be used in this protocol. Budesonide is a steroid and can suppress the immune reaction locally in the respiratory system. Formoterol is β2 agonist and can open airways. It also can bind to PL-pro and can neutralize the virus according to the published articles.

Registry
clinicaltrials.gov
Start Date
April 4, 2020
End Date
May 20, 2020
Last Updated
6 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Fasa University of Medical Sciences
Responsible Party
Principal Investigator
Principal Investigator

Dr. Siamack Afazeli

Doctor

Fasa University of Medical Sciences

Eligibility Criteria

Inclusion Criteria

  • Definitely positive COVID-19 patients

Exclusion Criteria

  • Patients with acute respiratory problems including patients with:
  • Severe respiratory distress
  • Heamodynamic instabilitty
  • Acid base disturbance
  • Severe Anemia Patients with severe hepatic diseases Patients with Nurvous system diseases

Arms & Interventions

Levamisole Pill + Budesonide+Formoterol inhaler+Standard care

This group will take Levamisole + Budesonide/Formoterol along side with standard treatment regime.

Intervention: Levamisole Pill + Budesonide+Formoterol inhaler

Levamisole Pill + Budesonide+Formoterol inhaler+Standard care

This group will take Levamisole + Budesonide/Formoterol along side with standard treatment regime.

Intervention: Lopinavir/Ritonavir + hydoxychloroquine

Standard care

This group will take standard treatment regime introduced by Ministry of health.

Intervention: Lopinavir/Ritonavir + hydoxychloroquine

Outcomes

Primary Outcomes

Clear chest CT-scan

Time Frame: between 3-7 days

Chest Ct scan should be negative

PCR test

Time Frame: between 3-7 days

PCR test should be negative

Secondary Outcomes

  • Physical statues of patient(Between 3-7 days)

Study Sites (1)

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