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Trial · NCT07301034

Registered outcomes18

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

ListOutcomeTime frameDescription
PrimaryChange in percent atheroma volume (PAV) as determined by greyscale intravascular ultrasound (IVUS) in matched regions of interestFrom randomisation (week 0) to end-of-study (52-week)Percentage (%).
SecondaryChange in maximum lipid core burden index (LCBI) in any 4-mm segment(maxLCBI4mm) as determined by Near-infrared spectroscopy (NIRS) in matched regions of interestFrom randomisation (week 0) to end-of-study (52-week)Lipid core burden index (LCBI) (0 to 1000).
SecondaryChange in minimal fibrous cap thickness as determined by (optical coherence tomography) OCT in matched regions of interestFrom randomisation (week 0) to end-of-study (52-week)Micro meter (µmeter).
SecondaryChange in lipid core burden index (LCBI) total as determined by NIRS in matched regions of interestFrom randomisation (week 0) to end-of-study (52-week)LCBI index (0 to 1000).
SecondaryChange in average angular extension (AAE) of macrophages as determined by OCT in matched regions of interestFrom randomisation (week 0) to end-of-study (52-week)Degrees (°).
SecondaryChange in normalized total atheroma volume (NTAV) by IVUS in matched regions of interestFrom randomisation (week 0) to end-of-study (52-week)Cubic Millimeter (mm3).
SecondaryChange in mean fibrous cap thickness as determined by OCT in matched region of interestFrom randomisation (week 0) to end-of-study (52-week)µmeter.
SecondaryChange in interleukin6 (IL-6)From randomisation (week 0) to week 4, and week 52Picograms per milliliter (pg/mL).
SecondaryChange in high-sensitivity C-reactive protein (hs-CRP)From randomisation (week 0) to week 4, and week 52Milligrams per deciliter (mg/dL).
SecondaryChange in high-sensitivity Troponin T (hs-TnT)From randomisation (week 0) to week 4, and week 52Nanograms per milliliter (ng/mL).
SecondaryChange in N-terminal-pro-brain natriuretic peptide (NT-pro-BNP)From randomisation (week 0) to week 4, and week 52Picograms per milliliter (pg/mL).
SecondaryChange in lipid and inflammatory markersFrom randomisation (week 0) to week 4, and week 52
SecondaryTime to first occurrence of: All-cause deathFrom randomisation (week 0) to end-of-study (52 weeks)Number of first occurrences and time-to-event.
SecondaryTime to first occurrence of: Cardiac deathFrom randomisation (week 0) to end-of-study (52-week)Number of first occurrences and time-to-event.
SecondaryTime to first occurrence of:Non-fatal spontaneous myocardial infarctionFrom randomisation (week 0) to end-of-study (52-week)Number of first occurrences and time-to-event.
SecondaryTime to first occurrence of: Any coronary revascularizationFrom randomisation (week 0) to end-of-study (52-week)Number of first occurrences and time-to-event.
SecondaryTime to first occurrence of: Non-fatal strokeFrom randomisation (week 0) to end-of-study (52-week)Number of first occurrences and time-to-event.
SecondaryTime to first occurrence of:Transient ischemic attackFrom randomisation (week 0) to end-of-study (52-week)Number of first occurrences and time-to-event.

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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GET https://conductscience.org/api/trials/v1/NCT07301034/registered