Asymptomatic COVID-19 Trial

SARS-CoV-2 Infection Clinical Trial

— ACT  

Official title:

RCT in Asymptomatic Volunteers With COVID-19 Comparing Azithromycin and Hydroxychloroquine vs. Hydroxychloroquine Alone vs Standard of Care Without Antibiotics

Clinical Trial Details — Status: Withdrawn

Administrative data

• NCT number: NCT04374552
• Other study ID #: Pro2020000872
• Status: Withdrawn
• Phase: Phase 2
• Start date: May 5, 2020
• Est. completion date: April 2021

Study information

• Verified date: May 2020
• Source: Rutgers, The State University of New Jersey
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The coronavirus disease-2019 (COVID-19) is spreading throughout the United States. While there are no known therapies to treat those who have become sick, there have been some reports that a medication currently used to treat rheumatoid arthritis, lupus, and malaria (Hydroxychloroquine sulfate, also known as Plaquenil) may help to lessen the chance or severity of illness, especially if combined with a medicine that treats other kinds of infections (Azithromycin, also known as Zithromax or Zmax or Zpak).

There are some people who test positive for the virus but who are otherwise not ill. Current standard of care is to advise these people to self-monitor but no treatment is offered. It is not known how many of these individuals will remain symptom free, and how many will become sick or how severe those symptoms will be. This study will randomize those people who do not have symptoms into one of three treatment plans 1) Hydroxycholoquine and Azithromycin, or 2) no active medication (placebo). All participants will be followed for 2 months.

The study will determine if there is any benefit to those who are asymptomatic to taking taking Hydroxychloroquine sulfate in combination with Azithromycin, or if there is no benefit from taking these medications.

Description:

Participants will be randomized into one of two treatment plans

1. Hydroxycholoquine sulfate in combination with Azithromycin Hydroxycholorquine as above, plus Azithromycine: 500 mg po for day 1and then 250 mg QD for 4 days

2. no active medication (placebo)

All participants will be followed for 2 months. The primary aim is to determine if there is any benefit (reduced likelihood for development of fever and other symptoms of COVID-19 ) to taking only Hydroxychloroquine sulfate, or to taking Hydroxychloroquine sulfate in combination with Azithromycin, or if there is no benefit to taking these medications for this population.

Recruitment information / eligibility

• Status: Withdrawn
• Enrollment: 0
• Est. completion date: April 2021
• Est. primary completion date: November 2020
• Accepts healthy volunteers: No
• Gender: All
• Age group: 20 Years and older

Eligibility

Inclusion Criteria:

1. Documented SARS-CoV-2 infection by qPCR assay without symptoms consistent with COVID-19 within 1 week of enrollment

2. Age =20

Exclusion Criteria:

1. Retinal eye disease

2. Known glucose-6 phosphate dehydrogenase (G-6-PD) deficiency

3. Known chronic kidney disease, stage 4 or 5 or receiving dialysis

4. Current use of:

• Class 3 AAD - amiodarone, dronaderone, dofetilide, sotalol)

• Class 1A AAD (procainamide, quinidine, disopyramide)

• Flecainide

• chlorpromazine

• Cilostazol (Pletal)

• Donepezil (Aricept)

• Droperidol

• Fluconazole

• Methadone

• Ondansetron(Zofran)

• Thioridazine

• Macrolides (clarithromycin, erythromycin)

• Fluroquinolones (ciprofloxacin, levofloxacin, moxifloxacin)

5. Pregnancy or women who are breast feeding

6. Inability to tolerate oral medications

7. Allergy or prior adverse reaction to either azithromycin or hydroxychloroquine sulfate

8. Allergy to adhesives

9. QTc interval > 450 mSEC for men and women

10. History of Torsade de Pointes VT or prior cardiac arrest or congenital long QT interval

11. Non-English-speaking

Related Conditions & MeSH terms

• SARS-CoV-2 Infection

Intervention

Drug:
• Hydroxychloroquine sulfate &Azithromycin
Drug - Hydroxychloroquine sulfate &Azithromycin
• Placebo
Drug - placebo

Locations

Country	Name	City	State
United States	Robert Wood Johnson University Hospital	New Brunswick	New Jersey

Sponsors (1)

Lead Sponsor	Collaborator
Rutgers, The State University of New Jersey

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	The primary outcome is the rate of decline in viral load over the 10 days after randomization	Change in SARS-CoV-2 viral from baseline to day 6	10 days