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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04403555
Other study ID # tanta covid treatment
Secondary ID
Status Completed
Phase Phase 2/Phase 3
First received
Last updated
Start date June 1, 2020
Est. completion date December 1, 2020

Study information

Verified date July 2021
Source Tanta University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Efficacy of Ivermectin in COVID-19 treatment


Description:

Clinical Study Evaluating the Efficacy of Ivermectin in COVID-19 treatment


Recruitment information / eligibility

Status Completed
Enrollment 164
Est. completion date December 1, 2020
Est. primary completion date October 31, 2020
Accepts healthy volunteers No
Gender All
Age group N/A and older
Eligibility Inclusion Criteria: - All Adult Patients aging from 20 to 65 years-old with COVID-19 confirmed by pharyngeal swab PCR. Exclusion Criteria: - Allergy or contraindication to the drugs used in the study. - Pregnant and lactating mothers. - Patients with cardiac problems.

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Ivermectin
Ivermectin treatment

Locations

Country Name City State
Egypt Sherief Abd-Elsalam Tanta

Sponsors (1)

Lead Sponsor Collaborator
Tanta University

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Primary The number of patients with mortality Improvement of survival 1 month
Secondary Length of hospital stay Effect on the length of hospital stay 1 month
Secondary The need for mechanical ventilation Need for mechanical ventilation 1 month
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