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Trial · NCT03185481

Results by group81

Each measurement the trial posted, group by group, in the words and numbers it posted.

OutcomeGroupCategoryValueSpreadUnits
Number of Participants With Treatment-Emergent Adverse Events (All Causalities)PF-06649751 15 mg3Participants
Number of Participants With Treatment-Emergent Adverse Events (Treatment Related)PF-06649751 15 mg2Participants
Number of Participants With Clinically Significant Findings in Physical ExaminationPF-06649751 15 mg0Participants
Number of Participants With Clinically Significant Findings in Neurological ExaminationPF-06649751 15 mg0Participants
Number of Participants With Abnormalities in Laboratory Test (Without Regard to Baseline Abnormality)PF-06649751 15 mg1Participants
Number of Participants With Vital Signs Data Meeting Pre-defined CriteriaPF-06649751 15 mgStanding DBP increase from baseline >= 20 mm Hg0Participants
Number of Participants With Vital Signs Data Meeting Pre-defined CriteriaPF-06649751 15 mgStanding SBP increase from baseline >= 30 mm Hg1Participants
Number of Participants With Vital Signs Data Meeting Pre-defined CriteriaPF-06649751 15 mgSupine DBP increase from baseline >= 20 mm Hg0Participants
Number of Participants With Vital Signs Data Meeting Pre-defined CriteriaPF-06649751 15 mgSupine SBP increase from baseline >= 30 mm Hg2Participants
Number of Participants With Vital Signs Data Meeting Pre-defined CriteriaPF-06649751 15 mgStanding DBP decrease from baseline >= 20 mm Hg0Participants
Number of Participants With Vital Signs Data Meeting Pre-defined CriteriaPF-06649751 15 mgStanding SBP decrease from baseline >= 30 mm Hg0Participants
Number of Participants With Vital Signs Data Meeting Pre-defined CriteriaPF-06649751 15 mgSupine DBP decrease from baseline >= 20 mm Hg0Participants
Number of Participants With Vital Signs Data Meeting Pre-defined CriteriaPF-06649751 15 mgSupine SBP decrease from baseline >= 30 mm Hg0Participants
Number of Participants With Vital Signs Data of Orthostatic Hypotension Meeting Pre-defined CriteriaPF-06649751 15 mgDBP postural difference>=10 mm Hg(Supine-Standing)3Participants
Number of Participants With Vital Signs Data of Orthostatic Hypotension Meeting Pre-defined CriteriaPF-06649751 15 mgSBP postural difference>=20 mm Hg(Supine-Standing)4Participants
Number of Participants With Electrocardiogram Data Meeting Pre-defined CriteriaPF-06649751 15 mgPR Interval (aggregate) >= 300 msec0Participants
Number of Participants With Electrocardiogram Data Meeting Pre-defined CriteriaPF-06649751 15 mgQRS Duration (aggregate) >= 140 msec0Participants
Number of Participants With Electrocardiogram Data Meeting Pre-defined CriteriaPF-06649751 15 mgQT Interval (aggregate) >= 500 msec0Participants
Number of Participants With Electrocardiogram Data Meeting Pre-defined CriteriaPF-06649751 15 mgQTcF Interval (aggregate) >= 450 msec, <480msec0Participants
Number of Participants With Electrocardiogram Data Meeting Pre-defined CriteriaPF-06649751 15 mgQTcF Interval (aggregate) >= 480 msec, <500msec0Participants

Source ClinicalTrials.govtrials-2026-11-12-0.4.0

Sources 3

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNone 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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