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Efficacy of Ivermectin in COVID-19

Primary Purpose

Safety, SARS-CoV2 Infection, Ivermectin Poisoning

Status
Completed
Phase
Phase 1
Locations
Thailand
Study Type
Interventional
Intervention
Ivermectin
Placebo
Sponsored by
Bangkok Metropolitan Administration Medical College and Vajira Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Safety focused on measuring efficacy, ivermectin, covid-19, randomised controlled trial

Eligibility Criteria

18 Years - 80 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • adult men and women age 18-80 years
  • non-pregnant or breast-feeding women
  • had mild to moderate symptoms as defined by the World Health Organization (WHO) severity score for COVID-19 Mild disease was defined as cough , runny nose,anosmia, fever, diarrhea without dyspnea or tachypnea.

Moderate disease was defined as pneumonia but with oxygen saturation more than 90 percent

Exclusion Criteria:

  • were allergic to ivermectin
  • have the potential for a drug-drug interaction with ivermectin such as tamoxifen or warfarin
  • previously treated with ivermectin in the last 7 days
  • had received any herbal medicine
  • had severe chronic illness (severe congestive heart failure, chronic kidney disease stage 4-5, chronic liver disease, terminal cancer diseases)
  • had concurrent bacterial infection or unwilling to participate in the trial
  • Patients with severe symptoms, likely due to cytokine release syndrome
  • uncontrolled co-morbidities and immunocompromised states

Sites / Locations

  • Thananda Trakarnvanich

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Placebo Comparator

Arm Label

Ivermectin

Placebo

Arm Description

Ivermectin 12 mg per day for 5 plus standard care

Placebo plus standard care

Outcomes

Primary Outcome Measures

Viral clearance of SARS- CoV-2 intervention
Viral load from RT-PCR test
Viral clearance of SARS- CoV-2 intervention
Viral load from RT-PCR test

Secondary Outcome Measures

Duration of hospitalization
Day of hospitalization
frequency of clinical worsening
numbers of cases that have clinical worsening
Mechanical ventilation
numbers of cases that needs mechanical ventilation
Mortality rate
numbers of cases that died

Full Information

First Posted
October 8, 2021
Last Updated
December 14, 2021
Sponsor
Bangkok Metropolitan Administration Medical College and Vajira Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT05076253
Brief Title
Efficacy of Ivermectin in COVID-19
Official Title
Efficacy and Safety of Ivermectin in Treatment of Mild to Moderate COVID-19 Infection: a Randomized ,Double Blind,Placebo,Controlled Trial
Study Type
Interventional

2. Study Status

Record Verification Date
December 2021
Overall Recruitment Status
Completed
Study Start Date
September 1, 2021 (Actual)
Primary Completion Date
December 1, 2021 (Actual)
Study Completion Date
December 1, 2021 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Bangkok Metropolitan Administration Medical College and Vajira Hospital

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The newly emerged corona virus disease 2019 (COVID-19) has spread to all over the world, with recent estimates of more than 236 million cases diagnosed and led to 4.8 million deaths as November 20211 .Therapeutic approaches are needed to improve outcomes in patients with COVID-19 since no antiviral agent has yet been proved to be conclusively beneficial in COVID-19 infection,especially in patients with mild to moderate degree of severity There has been growing interest in the anti-parasitic drug,ivermectin, which previously was studied as an antiviral, anti-inflammatory and anti-cancer actions2 .It was also reported to have an in-vitro activity against SARS-CoV-23 .Its antiviral properties was due to the action on importin 2/1 mediated nuclear transport. Ivermectin prevents the binding of viral proteins to importin 2/1 rendering the viral proteins unable to enter the nucleus and cause infection4. Several clinical studies have found a beneficial effect of ivermectin in COVID-195-9 However, some study did not find significant difference between the patient group receiving ivermectin and control group10 .Until now, the controlled trials evaluating ivermectin in COVID-19 are lacking. Ivermectin is safe, with reported side effect of less than 1%. Hence it is essential to conduct a clinical trial with ivermectin in patients with COVID-19 .The objective of this study is to establish the efficacy of ivermectin for COVID-19 patients with mild to moderate disease, compare to usual case alone.
Detailed Description
This study is a randomized, double-blind, placebo controlled trial conducted at Faculty of Medicine, Vajira Hospital, Navamindradhiraj University from September 2021 to the end of November 2021. The patients were randomized in permuted block of four in a randomized sequence prepared by the unblinded pharmacist in Microsoft excel12 .Allocation assignment was concealed from investigators and the patients. The patients were allocated into two groups : either to group A (Ivermectin arm) or to group B (control arm) as shown in Fig 1. The patients were randomized in a 1:1 ratio .Group A received ivermectin 12 mg per day for 5 days as recommended by previous studes13,14 plus standard care. Group B was to receive standard care alone which included favipiravir or andrographolide, corticosteroids, cetrizine and paracetamol.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Safety, SARS-CoV2 Infection, Ivermectin Poisoning, Effect of Drug
Keywords
efficacy, ivermectin, covid-19, randomised controlled trial

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 1, Phase 2
Interventional Study Model
Factorial Assignment
Model Description
a randomized ,double blind,placebo,controlled trial
Masking
ParticipantCare ProviderInvestigator
Masking Description
Group A: Ivermectin Group B: Placebo
Allocation
Randomized
Enrollment
72 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Ivermectin
Arm Type
Active Comparator
Arm Description
Ivermectin 12 mg per day for 5 plus standard care
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
Placebo plus standard care
Intervention Type
Drug
Intervention Name(s)
Ivermectin
Intervention Description
Ivermectin plus standard care
Intervention Type
Drug
Intervention Name(s)
Placebo
Intervention Description
Standard care
Primary Outcome Measure Information:
Title
Viral clearance of SARS- CoV-2 intervention
Description
Viral load from RT-PCR test
Time Frame
7 days
Title
Viral clearance of SARS- CoV-2 intervention
Description
Viral load from RT-PCR test
Time Frame
14 days
Secondary Outcome Measure Information:
Title
Duration of hospitalization
Description
Day of hospitalization
Time Frame
28 days
Title
frequency of clinical worsening
Description
numbers of cases that have clinical worsening
Time Frame
28 days
Title
Mechanical ventilation
Description
numbers of cases that needs mechanical ventilation
Time Frame
28 days
Title
Mortality rate
Description
numbers of cases that died
Time Frame
28 days

10. Eligibility

Sex
All
Gender Based
Yes
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: adult men and women age 18-80 years non-pregnant or breast-feeding women had mild to moderate symptoms as defined by the World Health Organization (WHO) severity score for COVID-19 Mild disease was defined as cough , runny nose,anosmia, fever, diarrhea without dyspnea or tachypnea. Moderate disease was defined as pneumonia but with oxygen saturation more than 90 percent Exclusion Criteria: were allergic to ivermectin have the potential for a drug-drug interaction with ivermectin such as tamoxifen or warfarin previously treated with ivermectin in the last 7 days had received any herbal medicine had severe chronic illness (severe congestive heart failure, chronic kidney disease stage 4-5, chronic liver disease, terminal cancer diseases) had concurrent bacterial infection or unwilling to participate in the trial Patients with severe symptoms, likely due to cytokine release syndrome uncontrolled co-morbidities and immunocompromised states
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Thananda Trakarnvanich, M.D.
Organizational Affiliation
Bangkok Metropolitan Administration and Vajira Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Thananda Trakarnvanich
City
Bangkok
ZIP/Postal Code
10300
Country
Thailand

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
Data will be made available upon request after publication
IPD Sharing Time Frame
After publication
Citations:
PubMed Identifier
25130507
Citation
Omura S, Crump A. Ivermectin: panacea for resource-poor communities? Trends Parasitol. 2014 Sep;30(9):445-55. doi: 10.1016/j.pt.2014.07.005. Epub 2014 Aug 12.
Results Reference
background
PubMed Identifier
29063617
Citation
Chen IS, Kubo Y. Ivermectin and its target molecules: shared and unique modulation mechanisms of ion channels and receptors by ivermectin. J Physiol. 2018 May 15;596(10):1833-1845. doi: 10.1113/JP275236. Epub 2017 Nov 9.
Results Reference
background
PubMed Identifier
33293006
Citation
Khan MSI, Khan MSI, Debnath CR, Nath PN, Mahtab MA, Nabeka H, Matsuda S, Akbar SMF. Ivermectin Treatment May Improve the Prognosis of Patients With COVID-19. Arch Bronconeumol (Engl Ed). 2020 Dec;56(12):828-830. doi: 10.1016/j.arbres.2020.08.007. Epub 2020 Sep 24. No abstract available.
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
PubMed Identifier
36028897
Citation
Manomaipiboon A, Pholtawornkulchai K, Poopipatpab S, Suraamornkul S, Maneerit J, Ruksakul W, Phumisantiphong U, Trakarnvanich T. Efficacy and safety of ivermectin in the treatment of mild to moderate COVID-19 infection: a randomized, double-blind, placebo-controlled trial. Trials. 2022 Aug 26;23(1):714. doi: 10.1186/s13063-022-06649-3.
Results Reference
derived

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Efficacy of Ivermectin in COVID-19

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