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| Methods | Randomised controlled trial Blinding not mentioned No mention of loss to follow‐up | |
| Participants | 14 patients with shock due to haemorrhage or sepsis | |
| Interventions | 1) HES (Hespan) 2) 5% Albumin Number in each group not reported | |
| Outcomes | Haemodynamic variables | |
| Notes | Follow‐up 4 hours post infusion | |
| Risk of bias | ||
| Bias | Authors' judgement | Support for judgement |
| Allocation concealment (selection bias) | Unclear risk | Unclear. No information given on method of allocation |
