Comparison · NCT03941288-2f2ea719
Functional Dyspepsia - Cannabidiol vs Functional Dyspepsia - Placebo: Weekly Global Symptom Assessment
Calculated by ConductScience from the counts the trial posted to ClinicalTrials.gov.
2 sourcestrial-comparisons-2026-03-23-0.1.0
Cite this record
ConductScience Library. Functional Dyspepsia - Cannabidiol vs Functional Dyspepsia - Placebo: Weekly Global Symptom Assessment. Trial comparisons, record NCT03941288-2f2ea719. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT03941288-2f2ea719
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Measures6
Calculated by ConductScience from the counts the trial posted to ClinicalTrials.gov.
| Measure | Value | 95% interval, lower | 95% interval, upper | Method | Note |
|---|---|---|---|---|---|
| Risk in group 1 | 0.48 | 0.3 | 0.665 | wilson | |
| Risk in group 2 | 0.478 | 0.292 | 0.67 | wilson | |
| Risk difference, group 1 minus group 2 | 0.00174 | -0.261 | 0.264 | newcombe hybrid score | |
| Risk ratio, group 1 over group 2 | 1 | 0.556 | 1.81 | log | |
| Odds ratio, group 1 over group 2 | 1.01 | 0.324 | 3.13 | log | |
| Number needed to treat, for one more participant with the outcome on Functional Dyspepsia - Cannabidiol than on Functional Dyspepsia - Placebo | 575 | from the risk difference interval | the interval includes no difference |
Source ClinicalTrials.gov
Groups2
Group 2 names the comparator: placebo.
| Group | Title | Description | With the outcome | Analysed | ClinicalTrials.gov code |
|---|---|---|---|---|---|
| Group 1 | Functional Dyspepsia - Cannabidiol | Cannabidiol will be administered to participants with functional dyspepsia orally twice daily in equally divided doses starting at 2.5mg/kg per day and increasing by 2.5 to 5.0mg/kg every other day until the target dose of 20mg/kg is reached. | 12 | 25 | OG000 |
| Group 2 | Functional Dyspepsia - Placebo | Placebo will be administered to participants with functional dyspepsia orally twice daily in equally divided doses starting at 2.5mg/kg per day and increasing by 2.5 to 5.0mg/kg every other day until the target dose of 20mg/kg is reached. | 11 | 23 | OG001 |
Source ClinicalTrials.gov
Outcome
- Type
- SECONDARY
- Title
- Weekly Global Symptom Assessment
- Description
The number of functional dyspepsia participants who confirmed adequate relief of dyspepsia symptoms, based on the self-reporting question In the past 7 days have you had adequate relief of your upper abdominal pain or discomfort?.
- Time frame
- 4 weeks
- Population
Source ClinicalTrials.gov
Trial
- Title
- Efficacy and Safety of Cannabidiol for Gastroparesis and Functional Dyspepsia
- NCT number
- NCT03941288
- Phases
- PHASE2
- Conditions
- Gastroparesis, Dyspepsia
- Interventions
- Cannabidiol, placebo
- Lead sponsor
- Mayo Clinic
- Results first posted
- 2024-02-13
- Results on ClinicalTrials.gov
- https://clinicaltrials.gov/study/NCT03941288?tab=results
Source ClinicalTrials.gov
Source
- Release
- trial-comparisons-2026-03-23-0.1.0
- Release manifest SHA-256
- f66225897fbf258b57ea10bdacfd0347d3cdfda93f7f5685234b7e06ea36fa57
- AACT copy
- 2026-03-23
- Tables read
- outcome_counts.parquet, outcome_measurements.parquet, outcomes.parquet, reported_event_totals.parquet, reported_events.parquet, result_groups.parquet, studies.parquet, ctgov_trial.parquet
Source ClinicalTrials.gov
Sources 2
- ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
- ClinicalTrials.govNo license stated
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
ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions. The measures are ConductScience's calculation from them.
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