Quinlan 2004.

Methods	Prospective, randomised, placebo‐controlled study.
Participants	Patients meeting the American European Consensus criteria for acute lung injury.
Interventions	1) Intervention (n=10) received albumin (25g of a 25% solution) every 8 hrs for a total of nine doses. 2) Control (n=10) received normal saline administered in identical fashion and volume.
Outcomes	Deaths noted.
Notes
Risk of bias
Bias	Authors' judgement	Support for judgement
Allocation concealment (selection bias)	Unclear risk	"Patients were randomized to receive 25g of human albumin every 8 hrs or a placebo (normal saline, administered in a double‐blind fashion and targeted to normalization of serum total protein." p. 755 ‐ 756.