MANS-NRIZ Trial for COVID-19 Treatment : Extension Study

  • STATUS
    Recruiting
  • End date
    Dec 21, 2022
  • participants needed
    100
  • sponsor
    Mansoura University
Updated on 21 July 2021

Summary

This search will focus on patients with COVID 19 infection this study is a prospective cohort study based on the analysis of response in comparative panel between two arm Nitazoxanide, Ribavirin and Ivermectin plus Zinc arm and other arm without any intervention as regards the safety and efficacy and cost effective result. Two years duration of the project would be enough to cover the stages of the work as shown below in the time plan. Initial stage of collecting materials and patients' clinical data, each patient will undergoes strict follow up period to reveal the clinical, laboratory and radiological response. The procedures are to be approved by the institutional ethical committee.

Description

This search will focus on patients with COVID 19 infection this study is a prospective cohort study based on the analysis of response in comparative panel between two arm Nitazoxanide, Ribavirin and Ivermectin plus Zinc arm and other arm without any intervention as regards the safety and efficacy and cost effective result. Two years duration of the project would be enough to cover the stages of the work as shown below in the time plan. Initial stage of collecting materials and patients' clinical data, each patient will undergoes strict follow up period to reveal the clinical, laboratory and radiological response. The procedures are to be approved by the institutional ethical committee.

Details
Condition COVID 19 Pneumonia
Treatment Ivermectin,ribavirin ,nitazoxanide and zinc
Clinical Study IdentifierNCT04959786
SponsorMansoura University
Last Modified on21 July 2021

Eligibility

Yes No Not Sure

Inclusion Criteria

Aged 18 years
Laboratory-confirmed SARS-CoV- 2 infection
Hospitalized patients
need reservoir mask for oxygen support
need HFNC for oxygen support

Exclusion Criteria

Mechanical ventilations for oxygen support
Inability to take oral medications
Pregnancy or breastfeeding
Clear my responses

How to participate?

Step 1 Connect with a study center
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  • You can expect the study team to contact you via email or phone in the next few days.
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Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.

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If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

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Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

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