Bellentani 1988.
| Methods | Blinding of randomisation: can't tell Blinding of intervention: no Complete follow‐up: yes Blinding of outcome measurement: can't tell | |
| Participants | 16 clinically stable low birth weight infants (gestational age 32 to 37 weeks). Infants were excluded if there was evidence of jaundice. | |
| Interventions | Treatment (N=8): Cow milk formula (Similac) with taurine added to a concentration of 45 milligrams/litre. Control (N=8): Same formula without added taurine. Intervention assigned for 20 days. | |
| Outcomes | Growth (weight gain) during the 20 days trial period, and biochemical measures of hepatic function. | |
| Notes | Setting: Instituto di Semeiotica Medica, Modena, Italia. | |
| Risk of bias | ||
| Bias | Authors' judgement | Support for judgement |
| Allocation concealment? | Unclear risk | B ‐ Unclear |