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Trial · NCT03040817

Registered outcomes15

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

ListOutcomeTime frameDescription
PrimaryChange from Baseline in Gastric Emptying Imaging at 6 months.From baseline to 6 months.Each participant will receive gastric emptying imaging measurement both at baseline and 6 months.
PrimaryChange from Baseline in Gastric Emptying Imaging at 12 months.From baseline to 12 months.Each participant will receive gastric emptying imaging measurement both at baseline and 12 months.
PrimaryChange from Baseline in Gastric Emptying Imaging at 24 months.From baseline to 24 months.Each participant will receive gastric emptying imaging measurement both at baseline and 24 months.
PrimaryChange from Baseline in Gastric Antrum Volume at 6 months.From baseline to 6 months.Each participant will receive gastric antrum volume measurement both at baseline and 6 months.
PrimaryChange from Baseline in Gastric Antrum Volume at 12 months.From baseline to 12 months.Each participant will receive gastric antrum volume measurement both at baseline and 12 months.
PrimaryChange from Baseline in Gastric Antrum Volume at 24 months.From baseline to 24 months.Each participant will receive gastric antrum volume measurement both at baseline and 24 months.
PrimaryChange from Baseline in Gastric Emptying Time at 6 months.From baseline to 6 months.Each participant will receive gastric emptying time measurement both at baseline and 6 months.
PrimaryChange from Baseline in Gastric Emptying Time at 12 months.From baseline to 12 months.Each participant will receive gastric emptying time measurement both at baseline and 12 months.
PrimaryChange from Baseline in Gastric Emptying Time at 24 months.From baseline to 24 months.Each participant will receive gastric emptying time measurement both at baseline and 24 months.
PrimaryChange from Baseline in Gastroparesis Cardinal Symptoms Index at 6 months.From baseline to 6 months.Each participant will receive gastroparesis cardinal symptoms index evaluation both at baseline and 6 months.
PrimaryChange from Baseline in Gastroparesis Cardinal Symptoms Index at 12 months.From baseline to 12 months.Each participant will receive gastroparesis cardinal symptoms index evaluation both at baseline and 12 months.
PrimaryChange from Baseline in Gastroparesis Cardinal Symptoms Index at 24 months.From baseline to 24 months.Each participant will receive gastroparesis cardinal symptoms index evaluation both at baseline and 24 months.
PrimaryChange from Baseline in Gastroesophageal Reflux Disease Questionnaire at 6 months.From baseline to 6 months.Each participant will receive gastroesophageal reflux disease questionnaire evaluation both at baseline and 6 months.
PrimaryChange from Baseline in Gastroesophageal Reflux Disease Questionnaire at 12 months.From baseline to 12 months.Each participant will receive gastroesophageal reflux disease questionnaire evaluation both at baseline and 12 months.
PrimaryChange from Baseline in Gastroesophageal Reflux Disease Questionnaire at 24 months.From baseline to 24 months.Each participant will receive gastroesophageal reflux disease questionnaire evaluation both at baseline and 24 months.

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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