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Dietary Supplement

Treatment Arm for Coronavirus

N/A
Waitlist Available
Led By James Veltmeyer, MD
Research Sponsored by Therapeutic Solutions International
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 12 weeks
Awards & highlights

Study Summary

This trial will test if a nutritional supplement can help reduce infection risk in people who are likely to get COVID-19.

Eligible Conditions
  • Coronavirus
  • Coronavirus Infection
  • COVID-19

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~12 weeks
This trial's timeline: 3 weeks for screening, Varies for treatment, and 12 weeks for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.
Primary outcome measures
Prevention of COVID-19
Secondary outcome measures
Safety as determined by presence or absence of Adverse Events and Serious Adverse Events

Trial Design

1Treatment groups
Experimental Treatment
Group I: Treatment ArmExperimental Treatment1 Intervention
Patients will receive 2 pills of QuadraMune(TM) daily for 12 weeks

Find a Location

Who is running the clinical trial?

Therapeutic Solutions InternationalLead Sponsor
2 Previous Clinical Trials
60 Total Patients Enrolled
James Veltmeyer, MDPrincipal InvestigatorTherapeutic Solutions International
1 Previous Clinical Trials
30 Total Patients Enrolled

Frequently Asked Questions

These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.
Recent research and studies
clinicaltrials.govStudy
QuadraMune(TM) for Prevention of COVID-19
2020. "QuadraMune(TM) for Prevention of COVID-19". ClinicalTrials.gov. https://clinicaltrials.gov/ct2/show/NCT04421391.
All > Covid
~103 spots leftby Apr 2025
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