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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04445311
Other study ID # ZU-IRB#6151/31-5-2020
Secondary ID
Status Recruiting
Phase Phase 2/Phase 3
First received
Last updated
Start date May 31, 2020
Est. completion date August 15, 2020

Study information

Verified date June 2020
Source Zagazig University
Contact Waheed Shouman, MD
Phone +201114812048
Email shouman66@gmail.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

confirmed cases with COVID-19 will receive ivermectin as a therapeutic option as well as standard of care treatment and will be compared to those that will receive only standard of care ttt


Recruitment information / eligibility

Status Recruiting
Enrollment 100
Est. completion date August 15, 2020
Est. primary completion date July 30, 2020
Accepts healthy volunteers No
Gender All
Age group 18 Years to 70 Years
Eligibility Inclusion Criteria:

COVID-19 patients during period of the study more than 18 years old

Exclusion Criteria:

refuse to participate pregnancy or lactation hypersensitivity to ivermectin receive any drug with interaction with ivermectin

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Ivermectin
3 successive days ttt of ivermectin started within 48 hours of symptoms

Locations

Country Name City State
Egypt Waheed Shouman Zagazig Sharkia

Sponsors (1)

Lead Sponsor Collaborator
Zagazig University

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Primary time to be symptoms free duration from day 1 symptoms till 3 days without symptoms within 21 days after enrollment
Secondary hospitalization need hospital admission within 21 days after enrollement
Secondary Mechanical ventilation need mechanical ventilation within 21 days after enrollement
Secondary length of stay days spent in hospital within one month days after enrollement
Secondary mortality survived or died within one month days after enrollement
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