Hydroxychloroquine vs Nitazoxanide in Patients With COVID-19
Primary Purpose
Coronavirus Infection
Status
Terminated
Phase
Phase 4
Locations
Mexico
Study Type
Interventional
Intervention
Nitazoxanide 500 MG
Hydroxychloroquine
Sponsored by
About this trial
This is an interventional treatment trial for Coronavirus Infection focused on measuring Treatment, Evolution
Eligibility Criteria
Inclusion Criteria:
- COVID-19 positive patients
- Treated at the Health Institute of the State of Mexico (ISEM).
- With risk factors to get complicated: age more than 60 years old, diabetes mellitus or obesity grade II or more.
Exclusion Criteria:
- Patients who have inherent contraindications to each drug.
Sites / Locations
- Materno-Perinatal Hospital "Mónica Pretelini"
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
Nitazoxanide + hydroxychloroquine
Hydroxychloroquine
Arm Description
Hydroxychloroquine 400 mg PO every 12 hours for two days and then 200 mg PO every 12 hours for four days + Nitazoxanide 500 mg PO every 6 hours for six days
Hydroxychloroquine 200 mg PO every 12 hours for 7 days
Outcomes
Primary Outcome Measures
Mechanical ventilation requirement
Percentage of patients COVID-19 positive that required mechanical ventilation
Secondary Outcome Measures
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT04341493
Brief Title
Hydroxychloroquine vs Nitazoxanide in Patients With COVID-19
Official Title
Treatment With Hydroxychloroquine vs Nitazoxanide + Hydroxychloroquine in Patients With COVID-19 With Risk Factors for Poor Outcome
Study Type
Interventional
2. Study Status
Record Verification Date
March 2021
Overall Recruitment Status
Terminated
Why Stopped
Concerns about safety of Hydroxychloroquine
Study Start Date
April 6, 2020 (Actual)
Primary Completion Date
August 30, 2020 (Actual)
Study Completion Date
December 30, 2020 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Hugo Mendieta Zeron
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
Coronaviruses (CoV) are positive-sense single-stranded RNA viruses that infect a wide range of hosts producing diseases ranging from the common cold to serious / fatal events. Nitazoxanide (NTZx) is a derivative of 5-nitrothiazole, synthesized in 1974 by Rosignol - Cavier. NTZx has powerful antiviral effects through the phosphorylation of protein kinase activated by double-stranded RNA, which leads to an increase in phosphorylated factor 2-alpha, an intracellular protein with antiviral effects. The purpose of this study is to contrast the beneficial effect of NTZx vs NTZx plus hydroxychloroquine in patients Coronavirus Disease (COVID-19) as well as against other treatments.
Detailed Description
Introduction The current pandemic caused by the SARS-COV2 coronavirus (COVID-19) is life-threatening and is challenging the world's best health systems. Accelerated spread of this pandemia led physicians to try a variety of treatments without a well established sequence due to ignorance about this new disease. The case fatality rate has been calculated at 2.2% but there are differences depending on the country affected.
Perspective When comparing the evolution of cases between Spain and Mexico, an apparently less pronounced trend is observed in Mexico, but this may be due to underdiagnosis. In calculations by the Mexican Ministry of Health, around 6% of the patients (approximately 10,500) who contract COVID-19 could be found serious and in need of hospitalization in intensive care.
NTZx NTZx and its circulating active metabolite, tizoxanide, inhibit the replication of a wide range of viruses, both RNA and DNA. It has action against 16 strains of Influenza A virus subtypes H1N1, H3N2, H3N2v, H3N8, H5N9, H7N1 and a strain of influenza B. It also works against respiratory syncytial virus, norovirus, dengue, yellow fever, Japanese encephalitis virus, rotavirus , hepatitis B and C, even against the human immunodeficiency virus (Severe Acute Respiratory Syndrome (SARS) and Middle East respiratory syndrome (MERS).
Problem Mexico is in Phase 2 according to the World Health Organization (WHO) and more local infections due to coronaviruses are expected. To date, various COVID-19 treatment schemes are being tested, but the usefulness of none can be assured.
When reviewing the drug schemes that are being carried out in the world, it calls the attention that developing countries are not included, beyond the fact that the tested alternatives are economically inaccessible.
This clinical survey aims to test the possible utility of NTZx against COVID-19, alone or in combination with hydroxychloroquine.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Coronavirus Infection
Keywords
Treatment, Evolution
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Model Description
In this study all patients with a COVID-19 positive result attended at the Health Institute of the State of Mexico (ISEM), will be invited to participate and offered one of two options that try to reduce the complications of this disease.
Masking
Participant
Masking Description
Patients won´t know whether the treatment they receive is hydroxychloroquine or nitazoxanide + hydroxychloroquine.
Allocation
Randomized
Enrollment
44 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Nitazoxanide + hydroxychloroquine
Arm Type
Experimental
Arm Description
Hydroxychloroquine 400 mg PO every 12 hours for two days and then 200 mg PO every 12 hours for four days + Nitazoxanide 500 mg PO every 6 hours for six days
Arm Title
Hydroxychloroquine
Arm Type
Active Comparator
Arm Description
Hydroxychloroquine 200 mg PO every 12 hours for 7 days
Intervention Type
Drug
Intervention Name(s)
Nitazoxanide 500 MG
Other Intervention Name(s)
hydroxychloroquine
Intervention Description
Clinical evaluation of patients with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) using this option with two drugs
Intervention Type
Drug
Intervention Name(s)
Hydroxychloroquine
Intervention Description
Clinical evaluation of patients with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) using this option with one drug
Primary Outcome Measure Information:
Title
Mechanical ventilation requirement
Description
Percentage of patients COVID-19 positive that required mechanical ventilation
Time Frame
Since the diagnosis until two weeks after
10. Eligibility
Sex
All
Minimum Age & Unit of Time
5 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
COVID-19 positive patients
Treated at the Health Institute of the State of Mexico (ISEM).
With risk factors to get complicated: age more than 60 years old, diabetes mellitus or obesity grade II or more.
Exclusion Criteria:
Patients who have inherent contraindications to each drug.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
José Meneses Calderón, MD
Organizational Affiliation
Hospital Materno-Perinatal "Mónica Pretelini Sáenz"
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Srivatsan Padmanabhan, MD, PhD
Organizational Affiliation
St. Joseph Medical Center
Official's Role
Principal Investigator
Facility Information:
Facility Name
Materno-Perinatal Hospital "Mónica Pretelini"
City
Toluca
ZIP/Postal Code
50130
Country
Mexico
12. IPD Sharing Statement
Plan to Share IPD
Yes
IPD Sharing Plan Description
If the final selected medical journal to send the paper of our research request it, we will add the full database of the studied population.
IPD Sharing Time Frame
After finishing the study.
IPD Sharing Access Criteria
Requested by the journal or after publication if any researcher in the world express interest if the information of this survey.
Citations:
PubMed Identifier
27095301
Citation
Rossignol JF. Nitazoxanide, a new drug candidate for the treatment of Middle East respiratory syndrome coronavirus. J Infect Public Health. 2016 May-Jun;9(3):227-30. doi: 10.1016/j.jiph.2016.04.001. Epub 2016 Apr 16.
Results Reference
background
PubMed Identifier
27585965
Citation
Mo Y, Fisher D. A review of treatment modalities for Middle East Respiratory Syndrome. J Antimicrob Chemother. 2016 Dec;71(12):3340-3350. doi: 10.1093/jac/dkw338. Epub 2016 Sep 1.
Results Reference
background
PubMed Identifier
32164080
Citation
Li H, Wang YM, Xu JY, Cao B. [Potential antiviral therapeutics for 2019 Novel Coronavirus]. Zhonghua Jie He He Hu Xi Za Zhi. 2020 Mar 12;43(3):170-172. doi: 10.3760/cma.j.issn.1001-0939.2020.03.004. Chinese.
Results Reference
background
PubMed Identifier
32513231
Citation
Calderon JM, Zeron HM, Padmanabhan S. Treatment with Hydroxychloroquine vs Hydroxychloroquine + Nitazoxanide in COVID-19 patients with risk factors for poor prognosis: A structured summary of a study protocol for a randomised controlled trial. Trials. 2020 Jun 8;21(1):504. doi: 10.1186/s13063-020-04448-2.
Results Reference
derived
Learn more about this trial
Hydroxychloroquine vs Nitazoxanide in Patients With COVID-19
We'll reach out to this number within 24 hrs