Elwood 1966.
Methods |
Design: randomised controlled trial Randomisation: individual Trial: daily oral iron versus placebo Date of study: not stated |
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Participants |
Setting: women living in a community near a clinic in Wales Malaria endemicity: not stated Included: women attended for a general checkup: recruited if haemoglobin 100 g/L to 135 g/L, along with a 1:2 ratio of women with haemoglobin > 135 g/L. Age range 15 years to 65 years (mean age not reported) Excluded: not stated Dropouts: 22 of 111 failed to complete study (group not stated) Sample size: total: 89; intervention: 40, control: 49 |
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Interventions |
Intervention: ferrous carbonate 200 mg daily Control: placebo Duration: 8 weeks |
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Outcomes | Haemoglobin, physical health, symptoms of anaemia (e.g. fatigue, concentration etc.) | |
Notes |
Compliance: not stated Conflicts of interest: not stated Funded by: trial drugs provided by Allen and Hanburys Other notes: not stated whether SD or SE used for error. Assumed to be SD |
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Risk of bias | ||
Bias | Authors' judgement | Support for judgement |
Random sequence generation (selection bias) | Unclear risk | Not reported |
Allocation concealment (selection bias) | Unclear risk | Not reported |
Blinding of participants and personnel (performance bias) All outcomes | Low risk | Placebo administered |
Blinding of outcome assessment (detection bias) All outcomes | Unclear risk | Not reported.Recording of symptoms could be influenced by knowledge of allocation |
Incomplete outcome data (attrition bias) All outcomes | Low risk | 111 enrolled, final data from 89 |
Selective reporting (reporting bias) | Low risk | Not evident |
Other bias | Low risk | Not evident |