Thorpe 1970.
Methods | R, DB, PC, parallel‐group study 1 episode treated with up to 2 doses of study medication. Capsules taken at onset on headache |
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Participants | Typical history of tension headache without other causes* n = 52 (completed to extent that reports could be analysed) No demographic data Baseline pain not reported |
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Interventions | Fiorinal‐Pa (aspirin + caffeine + isobutylallylbarbituric acid + paracetamol), n = 25 Placebo, n = 27 |
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Outcomes | PI: 5‐point scale 4 h after 1st dose Response = reduction ≥ 2 grades on PI AEs |
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Notes | * Lance JW. Treatment of chronic tension headache. Lancet 1964;1:1236‐9 Oxford Quality Score: R2, DB1, W0 |
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Risk of bias | ||
Bias | Authors' judgement | Support for judgement |
Random sequence generation (selection bias) | Low risk | "According to tables set out by Smart". Judged adequate |
Allocation concealment (selection bias) | Unclear risk | Not reported |
Blinding of participants and personnel (performance bias) All outcomes | Unclear risk | No details reported |
Blinding of outcome assessment (detection bias) All outcomes | Unclear risk | No details reported |
Incomplete outcome data (attrition bias) All outcomes | Unclear risk | Reported on participants who "completed to extent that reports could be analysed". Unclear what this means. No mention of withdrawals or imputation |
Size | High risk | < 50 participants per treatment arm (25‐27) |