Skip to content

Efficacy of Nano-Ivermectin Impregnated Masks in Prevention of Covid-19 Among Healthy Contacts and Medical Staff

Nano-Ivermectin Impregnated Masks Versus Ordinary Surgical Masks in Prevention of Covid-19 Among Healthy Contacts and Medical Staff

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04723459
Enrollment
150
Registered
2021-01-25
Start date
2021-01-23
Completion date
2021-03-28
Last updated
2021-03-17

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

Conditions

Covid-19

Keywords

Covid-19, antiviral mask, nano ivermectin

Brief summary

Antiviral efficacy of Ivermectin against Covid-19 in vitro was stated by many stusies all over the world with decreased effecacy in vivo so ,usage of masks impregnated into nano Ivermectin solution will theoretically increase the protective action of the ordinary masks

Detailed description

Antiviral effecacy of Ivermectin against Covid-19 in vitro was stated by many stusies all over the world with decreased effecacy in vivo so ,usage of masks impregnated into nano Ivermectin solution will theoretically increase the protective action of the ordinary masks this study is a trial for evaluation of adding a proved antiviral material to the mask and to compare between the protective value of this mask and the ordinary one.

Interventions

OTHERivermectin impregnated mask

mask with ivermectin nano solution

Sponsors

South Valley University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
NONE

Intervention model description

Sequential Assignment

Eligibility

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

Inclusion criteria

* health care personells and family contact of confirmed COVID-19 cases.

Exclusion criteria

* refusal of participate to use the masks. * pregnancy or lactation known hypersensitivity to ivermectin.

Design outcomes

Primary

MeasureTime frameDescription
Number of persons in each group who Complain of any suspected Symptomswithin 14 days after enrollement( Fever, Myalgia ,Cough, Sore Throat, Diarrhea, Shortness of Breath)

Secondary

MeasureTime frameDescription
Number of persons in each group who are diagnosed as COVID-19 patientswithin 21 days after enrollementswab test

Countries

Egypt

Contacts

Primary ContactZaky Aref
doctor.aref@hotmail.com+201001771210
Backup Contactmohammed hosny hassaan
mohammedhosnyhassaan@yahoo.com01115390073

Outcome results

None listed

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