Chanarin 1965.
Methods | The RCT was conducted on pregnant women coming to antenatal clinics at Saint Mary Hospital, London. | |
Participants | Pregnant women coming to antenatal clinic (n = 144). | |
Interventions | Women were allocated to 1 of the following 3 groups. Group 1: ferrous fumarate 100 mg (n = 50). Group 2: ferrous fumarate with 10 µg folic acid (n = 52). Group 3: lactose (n = 42). Subjects were asked to take 1 throughout pregnancy. |
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Outcomes | Mean urinary excretion (n = 144), mean haemoglobin (n = 144). | |
Notes | For this review, group 1 was compared with group 2. | |
Risk of bias | ||
Bias | Authors' judgement | Support for judgement |
Random sequence generation (selection bias) | Unclear risk | Quote: "women were allocated at random to one of the three groups". |
Allocation concealment (selection bias) | High risk | Insufficient information about allocation concealment. |
Blinding (performance bias and detection bias) All outcomes | Low risk | Quote: "Glaxo Laboratories supplied these drugs with green, blue or red labels and the precise contents of each batch being unknown to us during the trials". Comment: investigators blinded, it seem from the available information that it was a single blinded study. |
Incomplete outcome data (attrition bias) All outcomes | Unclear risk | Insufficient information. |
Selective reporting (reporting bias) | Unclear risk | Insufficient information. |
Other bias | Unclear risk | No other bias identified but insufficient information available to fully assess this 'Risk of bias' domain. |