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Completed

NCT Number: NCT04349592

Hydroxychloroquine With or Without Azithromycin for Virologic Cure of COVID-19

Q-PROTECT is a placebo controlled randomized trial (RCT) to ascertain the efficacy of hydroxychloroquine (HC) alone or, in combination with azithromycin (AZ), in reducing viral load in patients with COVID 19.

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Key information

About this study

Reducing viral load is potentially key to reducing viral transmission between humans. Observational data suggests HC and AZ may reduce the viral load. In this study we will randomise ambulatory patients with Covid 19 (confirmed by PCR in combination with clinical symptoms) to receive HC/AZ or HC/placebo or placebo for 7 days. On days 2-14, participants will be reviewed by a member of the research team and samples will be obtained for viral load, an ECG recorded and physical examination performed. On days 15-20, participants will be reviewed by telephone using a semi structured questionnaire. On day 21 participants will be examined in person and an oronasopharyngeal swabs obtained for PCR analysis. Participants will be followed for 6 months via their medical records.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Patient is in HMC facility for low-acuity, Covid-positive patients being quarantined.
  • Positive Covid test on qualitative assay used during routine care (i.e. not as part of Q-PROTECT)
  • Age at least 18

Exclusion criteria

  • Treating physician judges patient not appropriate for study participation for any reason
  • Age <18
  • Breastfeeding or pregnancy (patient-reported pregnancy status is sufficient)
  • Hypersensitivity to chloroquine or HC or AZ
  • History of or known QT prolongation
  • EKG required before study entry and on each visit during the subject's first seven days on pro-tocol, during the time period HC is being taken
  • Baseline QTc >480 if QRS width normal; QTc >510 if QRS >120
  • Known G6PD deficiency, porphyria, or retinopathy (eye exam prior to study entry)
  • Known hepatic or renal disease (or abnormality on liver or renal function testing at study day 1)
  • Low magnesium or low potassium (by testing on day 1)
  • Current (pre-study) therapy with antimalarial or dapsone
  • Current (pre-study) therapy with antiviral agents (e.g. oseltamivir)
  • Tisdale36 score exceeding 6 as tallied below (based on ACC recommendations)*
  • 1 point each: age>67, female sex, or being on loop diuretic
  • 2 points each: serum potassium <3.6, QTc>449, acute myocardial infarction
  • 3 points each: sepsis, heart failure, QT-prolonging drugs

Treatment and study plan

Hydroxychloroquine

Drug

Hydroxychloroquine 200 mg tablet oral, one tablet three times a day for 7 days

Other names: Plaquenil,

Azithromycin

Drug

Azithromycin 250 mg capsules oral, 2 capsules on day one, followed by 1 capsule once a day for days 2-5.

Other names: Zithromax, Azithrocin

Placebo tablet

Other

Oral, one tablet three times a day for 7 days

Placebo Capsules

Other

Oral 2 capsules on day one, followed by 1 capsule once a day for days 2-5.

Primary outcomes

  1. Proportion of virologically cured (PCR-negative status) as assessed on day six

    Time frame: Day 6

    Days

Secondary outcomes

  1. virologic cure on other study days

    Time frame: Day14 and Day 21

    Days

  2. virologic semiquantitative analysis of changing viral load

    Time frame: Day 1 to Day 21

    Days

  3. proportion of initially symtomatic subjects with disappearance of clinical symptoms

    Time frame: Day14 and Day 21

    Days

  4. proportion of initially asymtomatic subjects with appearance of new clinical symptoms

    Time frame: Day14 and Day 21

    Days

  5. proportions of subjects with potentially medication- related adverse events

    Time frame: 7 day

    grades

Sponsors and collaborators

Lead sponsor

Hamad Medical Corporation

Industry

Registry information

Official study title

Randomized Placebo-controlled Trial of Hydroxychloroquine With or Without Azithromycin for Virologic Cure of COVID-19

Important dates

Study start
2020
Primary completion
2020
Study completion
2020
First posted
Apr 16, 2020
Registry last updated
Feb 23, 2021

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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