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Trial · NCT04853199

Quercetin In The Treatment Of SARS-COV 2

NCT04853199, Early phase 1, Completed, Hôpital Universitaire Sahloul

3 sourcestrials-2026-11-12-0.5.0

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ConductScience Library. Quercetin In The Treatment Of SARS-COV 2. Trials, record NCT04853199. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT04853199

On this page

Trial

As registered on ClinicalTrials.gov, in the graph's capture of the registry.

Title
Quercetin In The Treatment Of SARS-COV 2
NCT number
NCT04853199
Status
Completed
Phases
Early phase 1
Enrollment
200 participants, actual
Lead sponsor
Hôpital Universitaire Sahloul
Conditions
SARS (Severe Acute Respiratory Syndrome)
Interventions
Quercetin, Placebo
First posted
2021-04-21
Last updated
2023-07-06

Source ClinicalTrials.gov

Registered outcomes7

Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.

ListOutcomeTime frameDescription
PrimaryMortality rate30 daysdeath rate
PrimaryNeed for ICU admission30 daysNumber of participants admitted to the Intensive care unit (ICU)
Primarytreatment safety30 daysrate of adverse events
SecondaryNeed for hospitalization for patients followed up at home30 daysNeed for hospitalization for patients followed up initially at home
Secondarylenghth of stay in Hospital30 daysdays spent at hospital for patients followed up initially at home
Secondaryresolution of COVID-19 symptoms30 daysTime to resolution of COVID-19 symptoms \[ Evaluated at day 15 and day 30 precising the Time at which the patient is completely symptom free and severity of symptoms
Secondaryneed for oxygen therapy30 daysNumber of participants who needed oxygen therapy

Outcomes0

Each outcome the trial posted results for, in ClinicalTrials.gov's words.

None in this release.

Results by group0

Each measurement the trial posted, group by group, in the words and numbers it posted.

None in this release.

Participant flow0

How many started, completed or left each group, period by period.

None in this release.

Adverse events0

Each adverse event the trial posted, group by group: the participants affected out of those at risk.

None in this release.

Adverse event totals0

The totals the trial posted for each group.

None in this release.

Papers0

The papers the trial lists on ClinicalTrials.gov.

None in this release.

Grants0

The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.

None in this release.

Trial comparisons0

Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.

None in this release.

Tests0

The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.

None in this release.

Data dates

The day each source was copied for this release.

ClinicalTrials.gov
2026-11-12
ClinicalTrials.gov
Results, from AACT
2026-03-23
AACT
NIH grant links
2026-11-13
NIH RePORTER

Sources 3

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNo license stated
  • NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
  • ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
  • ClinicalTrials.govnone stated
  • NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

For software

Read this trial from software.

The record and each of its lists are JSON, twenty rows a page. No key.

GET https://conductscience.org/api/trials/v1/NCT04853199

GET https://conductscience.org/api/trials/v1/NCT04853199/registered