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Trial · NCT04979221

Effect of Cyproheptadine on Ventilatory Support-free Days in Critically Ill Patients With COVID-19

NCT04979221, Phase 3, Unknown, Hospital de Clinicas de Porto Alegre

3 sourcestrials-2026-11-12-0.5.0

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ConductScience Library. Effect of Cyproheptadine on Ventilatory Support-free Days in Critically Ill Patients With COVID-19. Trials, record NCT04979221. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT04979221

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Trial

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

Title
Effect of Cyproheptadine on Ventilatory Support-free Days in Critically Ill Patients With COVID-19
NCT number
NCT04979221
Status
Unknown
Phases
Phase 3
Enrollment
274 participants, estimated
Lead sponsor
Hospital de Clinicas de Porto Alegre
Conditions
COVID-19 Pneumonia
Interventions
Cyproheptadine
First posted
2021-07-28
Last updated
2021-08-03

Source ClinicalTrials.gov

Registered outcomes8

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

ListOutcomeTime frameDescription
PrimaryVentilatory supportDay 28Number of days free from ventiltory support during the first 28 days
SecondaryMechanical ventilationThrough study completion, an average of 6 monthsDuration of mechanical ventilation
SecondaryMortality during 28 daysDay 28
SecondaryICU MortalityThrough study completion, an average of 6 months
SecondaryHospital MortalityThrough study completion, an average of 6 months
SecondaryLength of stay in the intensive care unitThrough study completion, an average of 6 months
SecondaryLength of stay in the hospitalThrough study completion, an average of 6 months
SecondaryRenal replacement therapyDay 28

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/NCT04979221

GET https://conductscience.org/api/trials/v1/NCT04979221/registered