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Trial · NCT03605680

Participant flow28

How many started, completed or left each group, period by period.

PeriodMilestoneGroupParticipantsUnits counted
SB Placebo Run-in Period (1 Week)STARTEDSingle-blind (SB) Run-in Period: Placebo604
SB Placebo Run-in Period (1 Week)STARTEDDouble-blind Treatment Period: Centanafadine SR 200 mg0
SB Placebo Run-in Period (1 Week)STARTEDDouble-blind Treatment Period: Centanafadine SR 400 mg0
SB Placebo Run-in Period (1 Week)STARTEDDouble-blind Treatment Period: Placebo0
SB Placebo Run-in Period (1 Week)TreatedSingle-blind (SB) Run-in Period: Placebo584
SB Placebo Run-in Period (1 Week)TreatedDouble-blind Treatment Period: Centanafadine SR 200 mg0
SB Placebo Run-in Period (1 Week)TreatedDouble-blind Treatment Period: Centanafadine SR 400 mg0
SB Placebo Run-in Period (1 Week)TreatedDouble-blind Treatment Period: Placebo0
SB Placebo Run-in Period (1 Week)COMPLETEDSingle-blind (SB) Run-in Period: Placebo466
SB Placebo Run-in Period (1 Week)COMPLETEDDouble-blind Treatment Period: Centanafadine SR 200 mg0
SB Placebo Run-in Period (1 Week)COMPLETEDDouble-blind Treatment Period: Centanafadine SR 400 mg0
SB Placebo Run-in Period (1 Week)COMPLETEDDouble-blind Treatment Period: Placebo0
SB Placebo Run-in Period (1 Week)NOT COMPLETEDSingle-blind (SB) Run-in Period: Placebo138
SB Placebo Run-in Period (1 Week)NOT COMPLETEDDouble-blind Treatment Period: Centanafadine SR 200 mg0
SB Placebo Run-in Period (1 Week)NOT COMPLETEDDouble-blind Treatment Period: Centanafadine SR 400 mg0
SB Placebo Run-in Period (1 Week)NOT COMPLETEDDouble-blind Treatment Period: Placebo0
Double-blind Treatment Period (6 Weeks)STARTEDSingle-blind (SB) Run-in Period: Placebo0
Double-blind Treatment Period (6 Weeks)STARTEDDouble-blind Treatment Period: Centanafadine SR 200 mg154
Double-blind Treatment Period (6 Weeks)STARTEDDouble-blind Treatment Period: Centanafadine SR 400 mg156
Double-blind Treatment Period (6 Weeks)STARTEDDouble-blind Treatment Period: Placebo156

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/NCT03605680/flow