Prophylaxis for COVID-19: Ivermectin in Close Contacts of COVID-19 Cases (IVERNEX-TUC) (IVERNEX-TUC)
Primary Purpose
Covid19
Status
Completed
Phase
Phase 2
Locations
Argentina
Study Type
Interventional
Intervention
Ivermectin
Placebo
Sponsored by

About this trial
This is an interventional prevention trial for Covid19 focused on measuring Ivermectin, Prophylaxis, COVID-19, Epidemiological link
Eligibility Criteria
Inclusion Criteria:
- Over 18 years either sex
- Women of childbearing age with a negative pregnancy test
- In close contact group or epidemiological nexus of a positive COVID-19 case
- Able to understand and grant informed consent
- Real-time - polymerase chain reaction test with a negative result
Exclusion Criteria:
- Known hypersensitivity or allergy to any component of the drug under evaluation
- Age under 18 years
- Use of immunosuppressants (including systemic corticosteroids) in the last 30 days
- Pregnant or lactating
- Patients with other acute infectious diseases
- Patients with autoimmune disease and/or chronic decompensated diseases
- Who have received a vaccine for COVID-19 (1/2 dose) or that have taken ivermectin (prior to 30 days of the study) or who are participating in another COVID-19 prophylaxis study
Sites / Locations
- SI.PRO.SA, Ministerio de Salud Pública
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Placebo Comparator
Arm Label
Experimental Group
Control Group
Arm Description
The EG receives ivermectin 0,6mg/kg of weight orally on days 1 (one) and 7 (seven) plus standard biosecurity care
The CG receives a placebo on days 1 (one) and 7 (seven) plus standard biosecurity care
Outcomes
Primary Outcome Measures
Number of subjects who were diagnosed with COVID-19 in EG and CG (Negative polymerase chain reaction - real-time).
Pearson's Chi-square and proportion test
Secondary Outcome Measures
Contagion risk.
Odd Ratio
Prophylactic effect associated with patient's preexisting comorbidity
Logistic regression test
Full Information
NCT ID
NCT04894721
First Posted
May 6, 2021
Last Updated
December 1, 2021
Sponsor
Ministry of Public Health, Argentina
1. Study Identification
Unique Protocol Identification Number
NCT04894721
Brief Title
Prophylaxis for COVID-19: Ivermectin in Close Contacts of COVID-19 Cases (IVERNEX-TUC)
Acronym
IVERNEX-TUC
Official Title
Study of Efficacy and Safety of Ivermectin for COVID-19 Prophylaxis in Post-exposure Contact or Epidemiological Link
Study Type
Interventional
2. Study Status
Record Verification Date
December 2021
Overall Recruitment Status
Completed
Study Start Date
June 1, 2021 (Actual)
Primary Completion Date
September 30, 2021 (Actual)
Study Completion Date
October 1, 2021 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Ministry of Public Health, Argentina
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
Randomized controlled clinical trial on using oral ivermectin in COVID-19 prophylaxis supplying the drug to close contacts of confirmed cases.
Detailed Description
This is a randomized, double-blind, and controlled clinical trial that aims to evaluate the use of oral ivermectin in COVID-19 prophylaxis. The study has two arms in a relationship of 2:1: Experimental Group (EG n=500) and Placebo Group (CG n=250).
The sample size was calculated by applying a two-proportion comparison test. Type of two-sided test, 95% confidence or safety level (1-α), 95% statistical power, 75% P1 (proportion in the placebo group), 65% P2 (proportion in the new treatment or intervention group), size sample without adjustment (n = 543), 25% expected proportion of losses, n= 724 sample adjusted for losses.
The hypothesis of the study is that treatment with ivermectin may decrease the chance of occurrence/progress of clinical manifestations and onset of severe disease. Whereas control of the contagion on the first days of development of the disease, this treatment with ivermectin in suspected cases of COVID-19 (by epidemiological nexus) would contribute to the control of contagion at the first part of the infection, even in the absence of symptoms.
Categorical variables will be represented with frequencies and proportions, while continuous quantitative variables will be expressed as mean ± standard deviation (SD) or as median and interquartile range (IQR). The proportions will be compared using Pearson's Chi-square test or Fisher's exact test as appropriate, and continuous quantitative variables with Student's t test. The estimation of the efficacy of intensive treatment with Ivermectin will be calculated using Kaplan-Meier curves and the differences will be analyzed by means of the log-rank test. The risk will be calculated as a ratio of advantages for Intensive treatment with Ivermectin (Odds Ratio, OR) with its 95% confidence intervals (95% CI). A value of p <0.05 will be considered significant. Analyzes will be performed using Stata 11.2 software.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Covid19
Keywords
Ivermectin, Prophylaxis, COVID-19, Epidemiological link
7. Study Design
Primary Purpose
Prevention
Study Phase
Phase 2, Phase 3
Interventional Study Model
Parallel Assignment
Model Description
Randomized controlled. Experimental and Control Group in relationship of 2:1
Masking
ParticipantCare ProviderInvestigator
Masking Description
Double-Blind
Allocation
Randomized
Enrollment
172 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Experimental Group
Arm Type
Experimental
Arm Description
The EG receives ivermectin 0,6mg/kg of weight orally on days 1 (one) and 7 (seven) plus standard biosecurity care
Arm Title
Control Group
Arm Type
Placebo Comparator
Arm Description
The CG receives a placebo on days 1 (one) and 7 (seven) plus standard biosecurity care
Intervention Type
Drug
Intervention Name(s)
Ivermectin
Other Intervention Name(s)
Iver
Intervention Description
0,6mg/kg of weight orally on days 1 and 7
Intervention Type
Other
Intervention Name(s)
Placebo
Intervention Description
A substance with similar physical characteristics as ivermectin, without the active drug ingredient
Primary Outcome Measure Information:
Title
Number of subjects who were diagnosed with COVID-19 in EG and CG (Negative polymerase chain reaction - real-time).
Description
Pearson's Chi-square and proportion test
Time Frame
At 2 weeks
Secondary Outcome Measure Information:
Title
Contagion risk.
Description
Odd Ratio
Time Frame
Up to 2 weeks
Title
Prophylactic effect associated with patient's preexisting comorbidity
Description
Logistic regression test
Time Frame
Up to 2 weeks
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
60 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
Over 18 years either sex
Women of childbearing age with a negative pregnancy test
In close contact group or epidemiological nexus of a positive COVID-19 case
Able to understand and grant informed consent
Real-time - polymerase chain reaction test with a negative result
Exclusion Criteria:
Known hypersensitivity or allergy to any component of the drug under evaluation
Age under 18 years
Use of immunosuppressants (including systemic corticosteroids) in the last 30 days
Pregnant or lactating
Patients with other acute infectious diseases
Patients with autoimmune disease and/or chronic decompensated diseases
Who have received a vaccine for COVID-19 (1/2 dose) or that have taken ivermectin (prior to 30 days of the study) or who are participating in another COVID-19 prophylaxis study
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Rossana Chahla, Ph. D
Organizational Affiliation
Ministry of Public Health, Tucumán, Argentina
Official's Role
Principal Investigator
Facility Information:
Facility Name
SI.PRO.SA, Ministerio de Salud Pública
City
Tucumán
ZIP/Postal Code
4000
Country
Argentina
12. IPD Sharing Statement
Plan to Share IPD
No
Citations:
PubMed Identifier
17687303
Citation
Chong CR, Sullivan DJ Jr. New uses for old drugs. Nature. 2007 Aug 9;448(7154):645-6. doi: 10.1038/448645a. No abstract available.
Results Reference
background
PubMed Identifier
32251768
Citation
Caly L, Druce JD, Catton MG, Jans DA, Wagstaff KM. The FDA-approved drug ivermectin inhibits the replication of SARS-CoV-2 in vitro. Antiviral Res. 2020 Jun;178:104787. doi: 10.1016/j.antiviral.2020.104787. Epub 2020 Apr 3.
Results Reference
background
PubMed Identifier
33278625
Citation
Ahmed S, Karim MM, Ross AG, Hossain MS, Clemens JD, Sumiya MK, Phru CS, Rahman M, Zaman K, Somani J, Yasmin R, Hasnat MA, Kabir A, Aziz AB, Khan WA. A five-day course of ivermectin for the treatment of COVID-19 may reduce the duration of illness. Int J Infect Dis. 2021 Feb;103:214-216. doi: 10.1016/j.ijid.2020.11.191. Epub 2020 Dec 2.
Results Reference
background
Citation
Ahmed Elgazzar, Basma Hany, Shaimaa Abo Youssef et al. Efficacy and Safety of Ivermectin for Treatment and prophylaxis of COVID-19 Pandemic, 13 November 2020, PREPRINT (Version 1) available at Research Square [https://doi.org/10.21203/rs.3.rs-100956/v1]
Results Reference
background
Citation
Hirsch RR, Carvallo, Héctor E. Ivermectin as Prophylaxis Against COVID-19 Retrospective Cases Evaluation. Microbiol Infect Dis. 2020; 4(4): 1-8.
Results Reference
background
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Prophylaxis for COVID-19: Ivermectin in Close Contacts of COVID-19 Cases (IVERNEX-TUC)
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