- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04403555
Ivermectin as a Novel Therapy in COVID-19 Treatment
July 29, 2021 updated by: Sherief Abd-Elsalam, Tanta University
The Efficacy of Ivermectin in COVID-19 Treatment
Efficacy of Ivermectin in COVID-19 treatment
Study Overview
Detailed Description
Clinical Study Evaluating the Efficacy of Ivermectin in COVID-19 treatment
Study Type
Interventional
Enrollment (Actual)
164
Phase
- Phase 2
- Phase 3
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
-
Tanta, Egypt
- Sherief Abd-Elsalam
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
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 Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: Ivermectin
Ivermectin plus standard of care treatment Dose 2 tablets 12mg per day for 3 days
|
Ivermectin treatment
Other Names:
|
No Intervention: Standard of care
Standard of care treatment
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
The number of patients with mortality
Time Frame: 1 month
|
Improvement of survival
|
1 month
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Length of hospital stay
Time Frame: 1 month
|
Effect on the length of hospital stay
|
1 month
|
The need for mechanical ventilation
Time Frame: 1 month
|
Need for mechanical ventilation
|
1 month
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: sherief Abd-Elsalam, Ass. Prof., ass. Prof. Tropical Medicine
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
June 1, 2020
Primary Completion (Actual)
October 31, 2020
Study Completion (Actual)
December 1, 2020
Study Registration Dates
First Submitted
May 23, 2020
First Submitted That Met QC Criteria
May 23, 2020
First Posted (Actual)
May 27, 2020
Study Record Updates
Last Update Posted (Actual)
August 2, 2021
Last Update Submitted That Met QC Criteria
July 29, 2021
Last Verified
July 1, 2021
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- tanta covid treatment
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
No
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
Clinical Trials on COVID
-
European Institute of OncologyFondazione I.R.C.C.S. Istituto Neurologico Carlo Besta; Azienda Ospedaliera... and other collaboratorsCompleted
-
Owlstone LtdCambridge University Hospitals NHS Foundation TrustCompleted
-
Erasmus Medical CenterDa Vinci Clinic; HGC RijswijkNot yet recruitingPost-COVID-19 Syndrome | Long COVID | Long Covid19 | Post COVID-19 Condition | Post-COVID Syndrome | Post COVID-19 Condition, Unspecified | Post-COVID ConditionNetherlands
-
Sultan Qaboos UniversityCompletedCOVID-19 | Non-CovidOman
-
Assiut UniversityRecruiting
-
Jilin UniversityUnknown
-
Indonesia UniversityRecruitingPost-COVID-19 Syndrome | Long COVID | Post COVID-19 Condition | Post-COVID Syndrome | Long COVID-19Indonesia
-
University of Roma La SapienzaQueen Mary University of London; Università degli studi di Roma Foro Italico; Bios Prevention SrlCompletedPost Acute Sequelae of COVID-19 | Post COVID-19 Condition | Long-COVID | Chronic COVID-19 SyndromeItaly
-
Miami VA Healthcare SystemNot yet recruiting
Clinical Trials on Ivermectin
-
Pierre Fabre DermatologyWithdrawn
-
Zydus Worldwide DMCCCatawba Research, LLCCompletedFacial RosaceaUnited States
-
Taro Pharmaceuticals USACompletedLice; Head LiceUnited States
-
Humanis Saglık Anonim SirketiCompleted
-
Assistance Publique - Hôpitaux de ParisCompletedIvermectin | Gale | Severe Forms of Scabies | Oral Parasitic DrugFrance
-
Mahidol UniversityMinistry of Health, ThailandUnknown
-
Actavis Inc.Teva Pharmaceuticals USACompleted
-
Wake Forest University Health SciencesGalderma R&DActive, not recruiting
-
South Valley UniversityRecruiting