Comparison · NCT02210000-sae
CAMICINAL 25 MG vs PLACEBO: serious adverse events
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. CAMICINAL 25 MG vs PLACEBO: serious adverse events. Trial comparisons, record NCT02210000-sae. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT02210000-sae
On this page
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 | 0.0517 | 0.0177 | 0.141 | wilson | |
| Risk in group 2 | 0.0357 | 0.00985 | 0.121 | wilson | |
| Risk difference, group 1 minus group 2 | 0.016 | -0.076 | 0.109 | newcombe hybrid score | |
| Risk ratio, group 1 over group 2 | 1.45 | 0.251 | 8.34 | log | |
| Odds ratio, group 1 over group 2 | 1.47 | 0.237 | 9.16 | log | |
| Number needed to harm, for one more participant with a serious adverse event on CAMICINAL 25 MG than on PLACEBO | 62.5 | 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 | CAMICINAL 25 MG | Eligible participants received oral Camicinal 25 mg once daily in the morning with 100 mL of water up to 84 days and were followed-up for 2 weeks. | 3 | 58 | EG000 |
| Group 2 | PLACEBO | Eligible participants received oral matching Placebo once daily in the morning with 100 mL of water up to 84 days and were followed-up for 2 weeks. | 2 | 56 | EG001 |
Source ClinicalTrials.gov
Harm
- What it counts
- Total, serious adverse events
- Time frame
- Up to end of follow up (100 days).
Source ClinicalTrials.gov
Trial
- Title
- A Study to Evaluate the Effect of Camicinal on Gastroparesis Symptoms in Type 1 and 2 Diabetic Subjects With Gastroparesis
- NCT number
- NCT02210000
- Phases
- PHASE2
- Conditions
- Gastroparesis
- Interventions
- Placebo, Camicinal
- Lead sponsor
- GlaxoSmithKline
- Results first posted
- 2017-11-01
- Results on ClinicalTrials.gov
- https://clinicaltrials.gov/study/NCT02210000?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.
For software
Read this comparison from software.
The record is JSON. No key.
GET https://conductscience.org/api/comparisons/v1/NCT02210000-sae