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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04723459
Other study ID # SVU MED CIT0 23 4 21 1 121
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date January 23, 2021
Est. completion date March 28, 2021

Study information

Verified date March 2021
Source South Valley University
Contact Zaky Aref
Phone +201001771210
Email doctor.aref@hotmail.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial 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


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.


Recruitment information / eligibility

Status Recruiting
Enrollment 150
Est. completion date March 28, 2021
Est. primary completion date February 19, 2021
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility 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.

Study Design


Related Conditions & MeSH terms


Intervention

Other:
ivermectin impregnated mask
mask with ivermectin nano solution

Locations

Country Name City State
Egypt Zaky Aref Qina

Sponsors (1)

Lead Sponsor Collaborator
South Valley University

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Primary Number of persons in each group who Complain of any suspected Symptoms ( Fever, Myalgia ,Cough, Sore Throat, Diarrhea, Shortness of Breath) within 14 days after enrollement
Secondary Number of persons in each group who are diagnosed as COVID-19 patients swab test within 21 days after enrollement
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