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Trial · NCT00272103

Itopride in Functional Dyspepsia:a Dose Finding Study

NCT00272103, Phase 2, Phase 3, Completed, Royal Adelaide Hospital

3 sourcestrials-2026-11-12-0.5.0

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ConductScience Library. Itopride in Functional Dyspepsia:a Dose Finding Study. Trials, record NCT00272103. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT00272103

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Trial

As registered on ClinicalTrials.gov, in the graph's capture of the registry.

Title
Itopride in Functional Dyspepsia:a Dose Finding Study
NCT number
NCT00272103
Status
Completed
Phases
Phase 2, Phase 3
Enrollment
500 participants
Lead sponsor
Royal Adelaide Hospital
Conditions
Functional Dyspepsia
Interventions
Itopride (drug)
First posted
2006-01-04
Last updated
2006-05-04

Source ClinicalTrials.gov

Registered outcomes5

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

ListOutcomeTime frameDescription
PrimaryAfter 8 weeks of treatment:
PrimaryChange of the severity of functional dyspepsia symptoms assessed by the Leeds Dyspepsia Questionnaire)
PrimaryPatient's global assessment of efficacy (proportion of patients symptom-free or markedly improved)
PrimaryImprovement of pain and/or fullness by at least one grade on a 5-grade scale.
SecondarySafety parameters

Outcomes0

Each outcome the trial posted results for, in ClinicalTrials.gov's words.

None in this release.

Results by group0

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

None in this release.

Participant flow0

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

None in this release.

Adverse events0

Each adverse event the trial posted, group by group: the participants affected out of those at risk.

None in this release.

Adverse event totals0

The totals the trial posted for each group.

None in this release.

Papers1

The papers the trial lists on ClinicalTrials.gov.

PMIDListed as
16495395RESULT

Source PubMed

Grants0

The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.

None in this release.

Trial comparisons0

Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.

None in this release.

Tests0

The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.

None in this release.

Data dates

The day each source was copied for this release.

ClinicalTrials.gov
2026-11-12
ClinicalTrials.gov
Results, from AACT
2026-03-23
AACT
NIH grant links
2026-11-13
NIH RePORTER

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.

For software

Read this trial from software.

The record and each of its lists are JSON, twenty rows a page. No key.

GET https://conductscience.org/api/trials/v1/NCT00272103

GET https://conductscience.org/api/trials/v1/NCT00272103/registered