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Trial · NCT01127607

Results by group244

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

OutcomeGroupCategoryValueSpreadUnits
Pittsburgh Side Effects Rating Scale - Percent Present for All Reported Adverse Events Occurring at a Rate of 5% or More50 mg Lisdexamfetamineworried/anxious14.3Percent of participants
Pittsburgh Side Effects Rating Scale - Percent Present for All Reported Adverse Events Occurring at a Rate of 5% or More70 mg Lisdexamfetamineworried/anxious17.6Percent of participants
Pittsburgh Side Effects Rating Scale - Percent Present for All Reported Adverse Events Occurring at a Rate of 5% or MoreNo Medicationdull, tired, listless10.5Percent of participants
Pittsburgh Side Effects Rating Scale - Percent Present for All Reported Adverse Events Occurring at a Rate of 5% or More30 mg Lisdexamfetaminedull, tired, listless16.7Percent of participants
Pittsburgh Side Effects Rating Scale - Percent Present for All Reported Adverse Events Occurring at a Rate of 5% or More50 mg Lisdexamfetaminedull, tired, listless9.5Percent of participants
Pittsburgh Side Effects Rating Scale - Percent Present for All Reported Adverse Events Occurring at a Rate of 5% or More70 mg Lisdexamfetaminedull, tired, listless11.8Percent of participants
Pittsburgh Side Effects Rating Scale - Percent Present for All Reported Adverse Events Occurring at a Rate of 5% or MoreNo Medicationheadaches5.3Percent of participants
Pittsburgh Side Effects Rating Scale - Percent Present for All Reported Adverse Events Occurring at a Rate of 5% or More30 mg Lisdexamfetamineheadaches36.1Percent of participants
Pittsburgh Side Effects Rating Scale - Percent Present for All Reported Adverse Events Occurring at a Rate of 5% or More50 mg Lisdexamfetamineheadaches28.6Percent of participants
Pittsburgh Side Effects Rating Scale - Percent Present for All Reported Adverse Events Occurring at a Rate of 5% or More70 mg Lisdexamfetamineheadaches29.4Percent of participants
Pittsburgh Side Effects Rating Scale - Percent Present for All Reported Adverse Events Occurring at a Rate of 5% or MoreNo Medicationstomachaches0.0Percent of participants
Pittsburgh Side Effects Rating Scale - Percent Present for All Reported Adverse Events Occurring at a Rate of 5% or More30 mg Lisdexamfetaminestomachaches16.7Percent of participants
Pittsburgh Side Effects Rating Scale - Percent Present for All Reported Adverse Events Occurring at a Rate of 5% or More50 mg Lisdexamfetaminestomachaches4.8Percent of participants
Pittsburgh Side Effects Rating Scale - Percent Present for All Reported Adverse Events Occurring at a Rate of 5% or More70 mg Lisdexamfetaminestomachaches29.4Percent of participants
Pittsburgh Side Effects Rating Scale - Percent Present for All Reported Adverse Events Occurring at a Rate of 5% or MoreNo Medicationcrabby, irritiable10.5Percent of participants
Pittsburgh Side Effects Rating Scale - Percent Present for All Reported Adverse Events Occurring at a Rate of 5% or More30 mg Lisdexamfetaminecrabby, irritiable27.8Percent of participants
Pittsburgh Side Effects Rating Scale - Percent Present for All Reported Adverse Events Occurring at a Rate of 5% or More50 mg Lisdexamfetaminecrabby, irritiable23.8Percent of participants
Pittsburgh Side Effects Rating Scale - Percent Present for All Reported Adverse Events Occurring at a Rate of 5% or More70 mg Lisdexamfetaminecrabby, irritiable23.5Percent of participants
Pittsburgh Side Effects Rating Scale - Percent Present for All Reported Adverse Events Occurring at a Rate of 5% or MoreNo Medicationtearful, sad, depressed7.9Percent of participants
Pittsburgh Side Effects Rating Scale - Percent Present for All Reported Adverse Events Occurring at a Rate of 5% or More30 mg Lisdexamfetaminetearful, sad, depressed13.9Percent of participants

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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