Comparison · NCT03285308-8ecff110
Relamorelin 10 μg vs Placebo: Number of Participants With Clinically Significant Abnormal Electrocardiogram (ECG) Results
Calculated by ConductScience from the counts the trial posted to ClinicalTrials.gov.
2 sourcestrial-comparisons-2026-03-23-0.1.0
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ConductScience Library. Relamorelin 10 μg vs Placebo: Number of Participants With Clinically Significant Abnormal Electrocardiogram (ECG) Results. Trial comparisons, record NCT03285308-8ecff110. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT03285308-8ecff110
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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 | 0.0184 | 0.00628 | 0.0527 | wilson | |
| Risk in group 2 | 0.0245 | 0.00958 | 0.0614 | wilson | |
| Risk difference, group 1 minus group 2 | -0.00613 | -0.0449 | 0.0313 | newcombe hybrid score | |
| Risk ratio, group 1 over group 2 | 0.75 | 0.171 | 3.3 | log | |
| Odds ratio, group 1 over group 2 | 0.745 | 0.164 | 3.38 | log | |
| Number needed to treat, for one fewer participant with the outcome on Relamorelin 10 μg than on Placebo | 163 | 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 | Relamorelin 10 μg | Following a 2-week placebo run-in, participants received relamorelin 10 μg injected subcutaneously twice daily for up to 12 weeks. | 3 | 163 | OG001 |
| Group 2 | Placebo | Following a 2-week placebo run-in, participants received placebo-matching relamorelin injected subcutaneously twice daily for up to 12 weeks. | 4 | 163 | OG000 |
Source ClinicalTrials.gov
Outcome
- Type
- SECONDARY
- Title
- Number of Participants With Clinically Significant Abnormal Electrocardiogram (ECG) Results
- Description
- A standard 12-lead ECG was performed. The investigator determined if the abnormal results were clinically significant.
- Time frame
- Up to 12 weeks
- Population
- Safety Population included all participants who received ≥1 administration of double-blind study treatment.
Source ClinicalTrials.gov
Trial
- Title
- A Safety and Efficacy Study of Relamorelin in Diabetic Gastroparesis 01
- NCT number
- NCT03285308
- Phases
- PHASE3
- Conditions
- Gastroparesis, Diabetes Mellitus
- Interventions
- Placebo, Relamorelin
- Lead sponsor
- Allergan
- Results first posted
- 2021-07-29
- Results on ClinicalTrials.gov
- https://clinicaltrials.gov/study/NCT03285308?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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