| Methods | Randomised, double blind, active control, cross-over (two 2 week periods - washout?). No follow up. Not enriched |
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| Participants | Trigeminal neuralgia. N = 12 Age 41-78 years. Male 5, Female 7. |
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| Interventions | CBZ to maximum tolerated dose Tocainide 20 mg/kg in 3 divided daily doses. Actual doses not reported |
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| Outcomes | TN score consisted of severity, frequency and duration of attacks | |
| Notes | Oxford Quality Score: R = 1, DB = 1, W = 0, Total = 2 Sponsored by Folsam Research Foundaton, Vivian L Smith Foundation |
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| Risk of bias | ||
| Bias | Authors’ judgement | Support for judgement |
| Random sequence generation (selection bias) | Unclear risk | ‘randomised double blind technique’ |
| Allocation concealment (selection bias) | Unclear risk | Not stated |
| Blinding (performance bias and detection bias) Active and controlled appeared similar |
Unclear risk | Stated as double blind but no further information |
| Duration | High risk | 2 week treatment |
| Outcome | Low risk | Individual start and end pain scores given |
| Incomple outcome assessment | Unclear risk | Not stated |
| Size | High risk | group size below 50 |