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Trial · NCT05050955

Registered outcomes11

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

ListOutcomeTime frameDescription
PrimaryALAD1 year post-transplantDiagnostic performance characteristics (sensitivity, specificity, PPV, NPV) of AlloSure Lung to detect acute lung allograft dysfunction (ALAD).
SecondaryChronic lung allograft dysfunction3 years post-transplantClinical diagnostic performance characteristics (sensitivity, specificity, PPV and NPV) of AlloSure Lung to detect chronic lung allograft dysfunction.
SecondaryAcute cellular rejection3 years post-transplantClinical diagnostic performance characteristics (sensitivity, specificity, PPV and NPV) of AlloSure Lung to detect acute cellular rejection (ACR).
SecondaryAntibody mediated rejection3 years post-transplantClinical diagnostic performance characteristics (sensitivity, specificity, PPV and NPV) of AlloSure Lung to detect antibody mediated rejection (AMR).
SecondaryAcute infection3 years post-transplantClinical diagnostic performance characteristics (sensitivity, specificity, PPV and NPV) of AlloSure Lung to detect acute infection.
SecondarySubject Variability3 years post-transplantDefine within-subject and between-subject variability of AlloSure Lung in clinically stable patients in order to establish reference change value RCV.
SecondaryALAD vs. Stability3 years post-transplantEvaluate the diagnostic performance characteristics of utilizing RCV to distinguish ALAD vs. Stability
SecondaryBiopsy-proven rejections3 years post-transplantThe proportion of biopsy-proven rejections with elevated AlloSure Lung versus those without elevated AlloSure-Lung.
SecondaryAlloSure Lung Results3 years post-transplantThe proportion of AlloSure Lung results obtained as surveillance or for-cause, that the physicians felt influenced their decisions around management of patients.
SecondaryALAD Free survival3 years post-transplantALAD free survival in lung transplant recipients who received AlloSure Lung as part of post-transplant surveillance.
SecondaryAlloSure Levels3 years post-transplantEvaluate AlloSure levels 30-90 days prior to acute rejection.

Source ClinicalTrials.govtrials-2026-11-12-0.5.0

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

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GET https://conductscience.org/api/trials/v1/NCT05050955/registered