Comparison · NCT04547192-sae
Mortality Pre-TIF Introduction vs Mortality Post-TIF Introduction: 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. Mortality Pre-TIF Introduction vs Mortality Post-TIF Introduction: serious adverse events. Trial comparisons, record NCT04547192-sae. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT04547192-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 | 0.0116 | 0.00781 | 0.0172 | wilson | |
| Risk in group 2 | 0.00299 | 0.00137 | 0.0065 | wilson | |
| Risk difference, group 1 minus group 2 | 0.00863 | 0.00345 | 0.0145 | newcombe hybrid score | |
| Risk ratio, group 1 over group 2 | 3.89 | 1.59 | 9.5 | log | |
| Odds ratio, group 1 over group 2 | 3.92 | 1.6 | 9.62 | log | |
| Number needed to harm, for one more participant with a serious adverse event on Mortality Pre-TIF Introduction than on Mortality Post-TIF Introduction | 116 | 69.1 | 290 | from the risk difference interval |
Source ClinicalTrials.gov
Groups2
Neither group, or both, names a comparator, so the groups keep ClinicalTrials.gov's order.
| Group | Title | Description | With the outcome | Analysed | ClinicalTrials.gov code |
|---|---|---|---|---|---|
| Group 1 | Mortality Pre-TIF Introduction | Patients who died at the study hospitals before TIF introduction. All 2,067 patients in this arm were at risk | 24 | 2,067 | EG000 |
| Group 2 | Mortality Post-TIF Introduction | Patients who died at the study hospitals after TIF introduction. All 2,010 patients in this arm were at risk | 6 | 2,010 | EG001 |
Source ClinicalTrials.gov
Harm
- What it counts
- Total, serious adverse events
- Time frame
- Patients were followed for adverse events until 18 months, when the last enrolled patient left hospital
Source ClinicalTrials.gov
Trial
- Title
- Improving Initial Management of the Injured at Ghanaian District and Regional Hospitals With a Trauma Intake Form
- NCT number
- NCT04547192
- Phases
- NA
- Conditions
- Behavior Problem
- Interventions
- Improving initial care of the injured
- Lead sponsor
- Kwame Nkrumah University of Science and Technology
- Results first posted
- 2024-01-02
- Results on ClinicalTrials.gov
- https://clinicaltrials.gov/study/NCT04547192?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/NCT04547192-sae