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Clinical Trial Details — Status: Enrolling by invitation

Administrative data

NCT number NCT04747678
Other study ID # ahmed19782020
Secondary ID
Status Enrolling by invitation
Phase
First received
Last updated
Start date February 3, 2021
Est. completion date March 1, 2021

Study information

Verified date February 2021
Source Menoufia University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational [Patient Registry]

Clinical Trial Summary

retrograde study of common and rare adverse effects of multiple doses of ivermectin used during the coivd 19 pandemic in egypt


Description:

ivermectin was used in Egypt during the pandemic of covid-19 and it was registered in the MOH protocol that has been published in November 2020 the study will document the adverse effects of many patients used ivermectin as aprophylaxis and as a treatment with multiple dose regimens


Recruitment information / eligibility

Status Enrolling by invitation
Enrollment 200
Est. completion date March 1, 2021
Est. primary completion date February 28, 2021
Accepts healthy volunteers
Gender All
Age group 16 Years to 80 Years
Eligibility Inclusion Criteria: - all people used ivermectin as a treatment or as a prophylactic in covid 19 pandemic in egypt with explained dose Exclusion Criteria: -

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Ivermectin
retrograde study of common and rare adverse effects of multiple doses of ivermectin used during the coivd 19 pandemic in egypt

Locations

Country Name City State
Egypt Ahmed Mansour Shibin Al Kawm Menoufia

Sponsors (1)

Lead Sponsor Collaborator
Menoufia University

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Primary all adverse effects will be collected from people used Ivermectin in between September 2020 to December 2020 all data will be collected from retrospective manner as a retrospective study the data will be collected from February 2021 to march 2021
Secondary all data will be arranged according to time and dose manner data for each dose will be identified together February to match 2021
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