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Inhaled Ivermectin and COVID-19

Efficacy and Safety of Inhaled Ivermectin in the Treatment of SARS-COV-2 (COVID-19)

Status
UNKNOWN
Phases
Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04681053
Acronym
CCOVID-19
Enrollment
80
Registered
2020-12-23
Start date
2021-02-25
Completion date
2021-12-31
Last updated
2021-02-24

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

Conditions

COVID-19

Keywords

COVID, Ivermectin, Inhalation, Antiviral, safety

Brief summary

Coronavirus disease-19 is global healthcare crisis. Till May 20, 2020, there were approximately 4,789,205 cases and 318,789 related mortalities were identified globally. This dramatic situation led to healthcare service collapse in many countries. Each country developed its own action plan depending on healthcare expertise and the available resources. There is no definitive therapy for Coronavirus disease-19 up till now. Many current and investigational drugs are used nowadays. Recent reports suggest a beneficial role of Ivermectin in the management of Coronavirus disease-19. A notice that necessitates further clinical studies. The aim of this study is to assess the efficacy and safety of the usage of inhaled ivermectin in the management of Coronavirus disease-19.

Detailed description

Coronavirus disease-19 (COVID-19) is a pandemic disease which is caused by the SARS-CoV2 virus. It is one of the biggest single-stranded RNA viruses. SARS-CoV2 Viral polyproteins are responsible for viral replication and transcription while its protease enzymes are responsible for polypeptides cleaving and immune system blockage. They are considered to be an important therapeutic target. Host immunological response against SARS-CoV2 could affect the disease outcome. Patients requiring ICU admission have higher levels of interleukins 6 - 10, tumor necrosis factor α (TNF-α), and fewer CD4+ and CD8+ T cells. The level of cytokines and lymphopenia is associated with pulmonary damage and respiratory distress. Till now, there is no definitive therapy for COVID-19. Multiple current and investigational drugs are used such as Hydroxychloroquine, lopinavir/ritonavir, and Remdesivir. Ivermectin: A potent anti-parasitic drug has shown to have an in-vitro antiviral activity against a broad range of viruses. It inhibits the interaction between the human immunodeficiency virus-1 (HIV-1) integrase protein (IN) and the importin (IMP) α/β1. But on the other hand, Ivermectin showed limited efficacy against DENV in phase III clinical trial that was done in Thailand in 2014-2017. Recent Studies proved the In-vitro effect and subsequently the possible therapeutic role of Ivermectin in the management of SARS-CoV2.

Interventions

DRUGIvermectin Powder

\- Administration through inhalation (6mg) BID for 3 days

Sponsors

Mansoura University
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Intervention model description

All current study participants will be classified into 4 equal groups : Group (A) received both oral and inhaled ivermectin in addition to the standard of care. Group (B)received inhaled ivermectin only Group (C) received oral ivermectin in addition to the standard of care, Group (D) received the current standard of care only

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
Yes

Inclusion criteria

* Both sexes * Age above 18 * Test positive for COVID-19 using Reverse transcription polymerase chain reaction (RT-PCR) prior to the start of study. * Willing to participate in the study * Mild to moderate severity index according to the WHO criteria

Exclusion criteria

* Hypersensitivity to the study drug. * History of co-morbid conditions such as: uncontrolled hypertension and diabetes, retinal problems and chronic liver and renal disease. * Women who are pregnant or breastfeeding.

Design outcomes

Primary

MeasureTime frameDescription
Rate of virological cure by Rt -PCR for COVID -19 using ivermectin when compared to standard treatmentthrougout the study completion up to one year(for every case must be done after 2 weeks from the start of treatment).All PCR for COVID-19 must be negative

Secondary

MeasureTime frameDescription
resolution of pneumoniathrougout the study completion up to one year (for every case must be done after 2 weeks from the start of treatment).The score severity index of pneumonia will be measured before and after receiving treatment by computed tomography (CT)(index from 0-20)increasing the index means increase severity.

Countries

Egypt

Contacts

Primary ContactMahmoud El-Bendary, M.D
mmelbendary@gmail.com00201002592205
Backup ContactHatem Elalfy
elalfy_hatem66@yahoo.com00201224790518

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026