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Ivermectin Nasal Spray for COVID19 Patients

Ivermectin Inhalation Forms in the Management of COVID-19 Egyptian Patients

Status
UNKNOWN
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04510233
Enrollment
60
Registered
2020-08-12
Start date
2020-09-30
Completion date
2020-12-31
Last updated
2020-08-12

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

Conditions

Covid19

Keywords

COVID19

Brief summary

The global escalation of COVID19 pandemic has put the health care system under pressure with urgent need for treatment. In the absence of vaccine and approved drug against SARS-COV2 over the past 6 months, the health authorities were obliged to re-purpose existing drugs to fight this pandemic.

Detailed description

Ivermectin is a well-known FDA-approved pan antiparasitic drug with high safety profile and potential therapeutic effects against COVID 19. It has been previously investigated as an antiviral agent. It showed 5000 fold reduction of SARS COV 2 viral RNA in-vitro studies. However, some researchers questioned its efficacy in the oral form as very high doses will be required to achieve a proper tissue concentration and viricidal effect in the respiratory system. Our hypothesis is that, since COVID-19 has shown to be particularly damaging to the respiratory system, using inhaled forms of Ivermectin will deliver the drug directly to the infection site and make it a treatment option.

Interventions

DRUGIvermectin nasal

Ivermectin nasal spray one ml in each nostril two times daily

DRUGIvermectin oral

Ivermectin oral (one tablet 6 mg three times daily)

OTHERstandard care

oxygen via masks or ventilators

Sponsors

Tanta University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 60 Years
Healthy volunteers
No

Inclusion criteria

* mild to moderate severity who are confirmed to be positive for SARS COV 2.

Exclusion criteria

* patients with severe form of COVID-19 or those who are on ventilatory support or those with cytokine storm

Design outcomes

Primary

MeasureTime frameDescription
PCR of SARS-Cov2 RNA14 daysNegative PCR result of SARS-Cov2 RNA in COVID19 patients

Contacts

Primary ContactKamal Okasha, PhD
okasha70@yahoo.com201140403709
Backup ContactNahla El-Ashmawy, PhD
nahlaelashmawy@yahoo.com201116721982

Outcome results

None listed

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