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Search / Trial NCT06817096

Efficacy and Safety of Nitazoxanide 600 Mg in the Outpatient Treatment of COVID-19 and Influenza

Launched by AZIDUS BRASIL · Feb 6, 2025

Trial Information

Current as of June 26, 2025

Not yet recruiting

Keywords

Nitazoxanide Outpatient Treatment

ClinConnect Summary

This clinical trial is studying the effectiveness and safety of a medication called nitazoxanide for treating COVID-19 and influenza in outpatient settings. Participants in the trial will take a dose of 600 mg of nitazoxanide, or a placebo (a dummy pill), twice a day for seven days. They will also keep a diary to track their symptoms and any other medications they are taking. After a week, they will visit the clinic for a check-up to assess their health and safety.

To participate, individuals must be at least 18 years old and have been diagnosed with COVID-19 or influenza within the last 48 hours. They cannot have certain health conditions, such as severe heart, liver, or kidney problems, or be pregnant or breastfeeding. This trial is not yet recruiting participants, but it aims to help understand if nitazoxanide can be a beneficial treatment for these viral infections.

Gender

ALL

Eligibility criteria

  • Inclusion Criteria:
  • Signed informed consent form;
  • Male or female;
  • Age ≥ 18 years;
  • COVID-19 or influenza diagnosed by rapid test, with symptom onset less than 48 hours ago;
  • Clinical condition compatible with outpatient treatment.
  • Exclusion Criteria:
  • Known hypersensitivity to nitazoxanide;
  • History of cardiomyopathies, hepatopathies, or nephropathies;
  • Antineoplastic treatment with chemotherapy or radiotherapy;
  • Severe autoimmune diseases with immunosuppression;
  • Transplant recipients;
  • Any uncompensated systemic disease at the investigator's discretion;
  • Participation in clinical studies in the last 12 months;
  • Pregnant or breastfeeding individuals;
  • Suspected bacterial coinfection or prescription of antibiotic therapy at enrollment;
  • Diagnosis of neurological disease (traumatic brain injury, stroke, Parkinson's disease, Alzheimer's disease, other dementias);
  • Diagnosis of developmental disorder (ADHD, ASD, learning disabilities, intellectual disability, Rett syndrome);
  • Significant hearing or vision impairment.

About Azidus Brasil

Azidus Brasil is a leading clinical research organization specializing in the development and management of clinical trials across various therapeutic areas. With a commitment to advancing healthcare, Azidus Brasil leverages its expertise in regulatory affairs, data management, and patient recruitment to deliver high-quality, efficient clinical study solutions. The organization collaborates with pharmaceutical and biotechnology companies to facilitate the successful progression of innovative therapies from initial research through to market authorization, ensuring adherence to the highest standards of ethics and scientific rigor.

Locations

Patients applied

0 patients applied

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported