Comparison · NCT00795366-sae
AVP, Arginine Vasopressin vs Standard Catecholamine: 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. AVP, Arginine Vasopressin vs Standard Catecholamine: serious adverse events. Trial comparisons, record NCT00795366-sae. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT00795366-sae
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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 | 0.143 | 0.0672 | 0.278 | wilson | |
| Risk in group 2 | 0.111 | 0.0519 | 0.222 | wilson | |
| Risk difference, group 1 minus group 2 | 0.0317 | -0.102 | 0.18 | newcombe hybrid score | |
| Risk ratio, group 1 over group 2 | 1.29 | 0.447 | 3.7 | log | |
| Odds ratio, group 1 over group 2 | 1.33 | 0.397 | 4.48 | log | |
| Number needed to harm, for one more participant with a serious adverse event on AVP, Arginine Vasopressin than on Standard Catecholamine | 31.5 | from the risk difference interval | the interval includes no difference |
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 | AVP, Arginine Vasopressin | Vasopressin, arginine vasopressin: Titrated to cerebral perfusion pressure greater than 60 mm Hg | 6 | 42 | EG000 |
| Group 2 | Standard Catecholamine | Standard catecholamine: Titrated catecholamine of attending physicians preference to cerebral perfusion pressure greater than 60 mm Hg. | 6 | 54 | EG001 |
Source ClinicalTrials.gov
Harm
- What it counts
- Total, serious adverse events
- Time frame
Adverse events were collected during the primary study period as the first 5 days of intracranial pressure monitoring while outcome data was also collected from admission until discharge from the hospital.
Source ClinicalTrials.gov
Trial
- Title
- Vasopressin Versus Catecholamines for Cerebral Perfusion Pressure Control in Brain Injured Trauma Patients
- NCT number
- NCT00795366
- Phases
- NA
- Conditions
- Traumatic Brain Injury
- Interventions
- arginine vasopressin, Standard catecholamine
- Lead sponsor
- University of Miami
- Results first posted
- 2014-12-12
- Results on ClinicalTrials.gov
- https://clinicaltrials.gov/study/NCT00795366?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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