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Trial · NCT03803007

Registered outcomes16

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

ListOutcomeTime frameDescription
PrimarySymptomatic intracranial haemorrhages24 hoursNumber of participants experiencing a symptomatic haemorrhage defined by a secondary increase in National Institute Health Stroke Scale score by 4 points or greater, or death
PrimaryIncidence of non-symptomatic intracranial haemorrhages24 hoursNon-symptomatic haemorrhages are those detected by Computerized Tomography scan
SecondaryChange from baseline of National Institute Health Stroke Scale score (7 minimum, 42 maximum), brain lesions and vessel recanalization24 hours
Absolute change from baseline of National Institute Health Stroke Scale score, change from baseline on brain lesions as assessed by Computerized Tomography scan or Magnetic Resonance Imaging or Magnetic Resonance Angiography, change from baseline on Recanalization as measured by the modified Thrombolysis In Cerebral Infarction score (0 minimum, 3 maximum) on Magnetic Resonance Angiography
SecondaryChange from baseline of National Institute Health Stroke Scale score (7 minimum, 42 maximum), brain lesions and vessel recanalization24 hours
Relative (%) change from baseline of National Institute Health Stroke Scale score, change from baseline on brain lesions as assessed by Computerized Tomography scan or Magnetic Resonance Imaging or Magnetic Resonance Angiography, change from baseline on Recanalization as measured by the modified Thrombolysis In Cerebral Infarction score (0 minimum, 3 maximum) on Magnetic Resonance Angiography
SecondaryChange from baseline of modified Ranking Scale score assessmentDay 90modified Ranking Scale score (0 minimum and 6 maximum): number of patients with favorable outcome (score 0-2)
SecondaryChange from baseline of modified Ranking Scale score assessmentDay 90modified Ranking Scale score (0 minimum and 6 maximum): percentage of patients with favorable outcome (score 0-2)
SecondaryChange from baseline on size of infarct zoneDay 7Change from baseline on size of infarct zone assessed by a central Magnetic Resonance Imaging review
SecondaryChange from baseline on vital signs6 hours, 24 hours, Day 7, Day 30 and Day 90Change from baseline on systolic and diastolic blood pressure
SecondaryChange from baseline on vital signs6 hours, 24 hours, Day 7, Day 30 and Day 90Change from baseline on heart rate
SecondaryChange from baseline on clinical laboratory assessmentsDay 90Change from baseline on plasma haemoglobin level
SecondaryChange from baseline on clinical laboratory assessmentsDay 90Change from baseline on platelet count
SecondaryChange from baseline on clinical laboratory assessmentsDay 90Change from baseline on serum glucose concentration
SecondaryChange from baseline on clinical laboratory assessmentsDay 90Change from baseline on serum creatinine concentration
SecondaryChange from baseline on ElectroCardioGram (ECG)24 hours and Day 90Change from baseline on 12-lead ElectroCardioGram (ECG)
SecondaryEvidence of anti-ACT017 antibodies (ADA)Day 30 and Day 90To assess evidence of anti-ACT017 antibodies (ADA) as a possible to ACT017 administration
SecondaryPharmacokinetics on ACT017 plasma concentration30 minutes, 9 hours and 24 hoursChange from baseline on ACT017 plasma concentration

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/NCT03803007/registered