Malay 1999.
| Methods | Single‐centre randomized controlled trial, general hospital; USA | |
| Participants | Adult surgical and trauma participants with septic shock (N = 10) | |
| Interventions | Fixed dose of vasopressin (0.04 U/min) vs placebo | |
| Outcomes | 24‐Hour mortality For the mortality analysis, we used data on 24‐hour mortality |
|
| Notes | Funding: not reported Conflict of interest. not reported |
|
| Risk of bias | ||
| Bias | Authors' judgement | Support for judgement |
| Random sequence generation (selection bias) | Low risk | Computer‐generated list |
| Allocation concealment (selection bias) | Low risk | Pharmacy controlled |
| Incomplete outcome data (attrition bias) All outcomes | Unclear risk | Not reported |
| Explicit in‐/exclusion criteria | Low risk | Described explicitly |
| ITT‐analysis | Unclear risk | Not reported |
| Adequate patient description | Low risk | Adequately reported |
| Identical care | Unclear risk | Not reported |
| Outcome description | Low risk | Clear |
| Physicians blinded | Low risk | Reported |
| Outcome assessors blinded? | Low risk | Reported |