Comparison · NCT05288348-7dbbb8cb
DSUVIA (Sufentanil) vs Standard Care: Number of Participants With Dizziness Requiring Treatment
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. DSUVIA (Sufentanil) vs Standard Care: Number of Participants With Dizziness Requiring Treatment. Trial comparisons, record NCT05288348-7dbbb8cb. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT05288348-7dbbb8cb
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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 | 0 | 0.0481 | wilson | |
| Risk in group 2 | 0.0135 | 0.00239 | 0.0727 | wilson | |
| Risk difference, group 1 minus group 2 | -0.0135 | -0.0727 | 0.0359 | newcombe hybrid score | |
| Risk ratio, group 1 over group 2 | log | a group has no participants with the outcome | |||
| Odds ratio, group 1 over group 2 | log | a cell of the two-by-two table is zero | |||
| Number needed to treat, for one fewer participant with the outcome on DSUVIA (Sufentanil) than on Standard Care | 74 | from the risk difference interval | the interval includes no difference |
Source ClinicalTrials.gov
Groups2
Group 2 names the comparator: standard care.
| Group | Title | Description | With the outcome | Analysed | ClinicalTrials.gov code |
|---|---|---|---|---|---|
| Group 1 | DSUVIA (Sufentanil) | Subjects will receive a single dose of 30 micrograms DSUVIA (sufentanil) tablet utilizing a sublingual applicator~Sufentanil 30 MCG Sublingual Tablet: 30 microgram sublingual tablet administered using sublingual applicator | 0 | 76 | OG000 |
| Group 2 | Standard Care | Subjects will receive standard care pain management~standard care pain treatment: standard care pain treatment given in Emergency Department | 1 | 74 | OG001 |
Source ClinicalTrials.gov
Outcome
- Type
- SECONDARY
- Title
- Number of Participants With Dizziness Requiring Treatment
- Description
- Dizziness requiring treatment
- Time frame
- from administration to ED discharge or rescue narcotic administered, whichever comes first (up to 120 minutes)
- Population
Source ClinicalTrials.gov
Trial
- Title
- DSUVIA Early Evaluation of Pain Trial
- NCT number
- NCT05288348
- Phases
- PHASE3
- Conditions
- Traumatic Injury
- Interventions
- Sufentanil 30 MCG Sublingual Tablet, standard care pain treatment
- Lead sponsor
- Frank Guyette
- Results first posted
- 2025-04-30
- Results on ClinicalTrials.gov
- https://clinicaltrials.gov/study/NCT05288348?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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