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Rapid Assessment of Potential Ischaemic Heart Disease With CTCA
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Trial · NCT02284191

Outcomes19

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

1 to 19 of 19

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TypeOutcomeTime framePopulationUnitsMeasured as
PRIMARYAll-cause Death or Subsequent Non-fatal Type 1 or Type 4b MI at One Year Measured as Time to First Such Event.1 year (post randomisation)All randomised participantsParticipantsCOUNT_OF_PARTICIPANTS
SECONDARYCoronary Heart Disease Death or Subsequent Non-fatal MI1 year (post randomisation)ParticipantsCOUNT_OF_PARTICIPANTS
SECONDARYCardiovascular Disease Death or Subsequent Non-fatal MI1 year (post randomisation)ParticipantsCOUNT_OF_PARTICIPANTS
SECONDARYSubsequent Non-fatal MI1 year (post randomisation)ParticipantsCOUNT_OF_PARTICIPANTS
SECONDARYCoronary Heart Disease Death1 year (post randomisation)ParticipantsCOUNT_OF_PARTICIPANTS
SECONDARYCardiovascular Death1 year (post-randomisation)ParticipantsCOUNT_OF_PARTICIPANTS
SECONDARYAll-cause Death1 year (post-randomisation)ParticipantsCOUNT_OF_PARTICIPANTS
SECONDARYCoronary Heart Disease (CHD) Death or Subsequent Non-fatal MI (Type 1 or 4b)1 year (post randomisation)ParticipantsCOUNT_OF_PARTICIPANTS
SECONDARYSubsequent Non-fatal MI (Type 1 or 4b)1 year (post-randomisation)ParticipantsCOUNT_OF_PARTICIPANTS
SECONDARYNon-cardiovascular Death1 year (post-randomisation)ParticipantsCOUNT_OF_PARTICIPANTS
SECONDARYInvasive Coronary Angiography1 year (post randomisation)ParticipantsCOUNT_OF_PARTICIPANTS
SECONDARYCoronary Revascularisation1 year (post randomisation)ParticipantsCOUNT_OF_PARTICIPANTS
SECONDARYPercutaneous Coronary Intervention1 year (post randomisation)ParticipantsCOUNT_OF_PARTICIPANTS
SECONDARYCoronary Artery Bypass Graft1 year (post randomisation)ParticipantsCOUNT_OF_PARTICIPANTS
SECONDARYNumber of Patients Prescribed ACS Therapies During Index Hospitalisation1 year (post randomisation)ParticipantsCOUNT_OF_PARTICIPANTS
SECONDARYDischarged on Preventative Treatment or Alteration in Dosage of Preventative Treatment During Index Hospitalisation1 year (post randomisation)ParticipantsCOUNT_OF_PARTICIPANTS
SECONDARYLength of Stay for Index HospitalisationA maximum follow up of one-year post-randomisation.daysMEDIAN
SECONDARYRepresentation or Rehospitalisation With Suspected ACS/ Recurrent Chest Pain After Index Hospitalisation1 year (post randomisation)ParticipantsCOUNT_OF_PARTICIPANTS
SECONDARYRadiation Exposure From CTCA as Trial Intervention1 year (post randomisation)Standard care group do not get CT so there is no data to analysemSvMEDIAN

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.

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