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Trial · NCT02973542

Registered outcomes15

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

ListOutcomeTime frameDescription
Primary30% reduction in abdominal painthrough study completion, an average of 12 weeks.
PrimaryScore of 4 or 5 on the SGA scalethrough study completion, an average of 12 weeks.
SecondaryMonthly assessment of abdominal painat 1 month
SecondaryMonthly assessment of score of Bristol scaleat 1 month
SecondaryMonthly evaluation of GIQLI questionnaireat 1 month
SecondaryMonthly evaluation of EQ-5D questionnaireat 1 month
SecondaryMonthly evaluation of IBS-SSS questionnaireat 1 month
SecondaryMonthly evaluation of SGA scale.at 1 month
SecondaryMonthly evaluation of the use of analgesicsat 1 month
SecondaryMonthly evaluation of the use of antispasmodicat 1 month
SecondaryMonthly evaluation of the use of regulators transit.at 1 month
SecondaryMonthly evaluation of medical response rateat 1 month
SecondaryMonthly evaluation of stop work related to IBS.at 1 month
SecondaryEvaluation of the tolerance of ethosuximide throughout the study.at 1 month
SecondaryEvaluation of the discontinuation rate study because of adverse events throughout the studyat 1 month

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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