NCT00475904.
Methods | Randomised, double‐blind, double‐dummy, placebo‐controlled, parallel groups, 4 weeks, not enriched | |
Participants | PHN ≥ 3 months after healing of rash. Age ≥ 18 years N = 360 Mean age 53 years, 38% women |
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Interventions | Gabapentin 1800 mg daily, n = 144 Topical cream with amitriptyline and ketamine, n = 140 Placebo for oral and topical cream, n = 76 |
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Outcomes | Mean reduction in PI from baseline | |
Notes | Oxford Quality Score: R = 1, DB = 2, W = 1, Total = 4 | |
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 (performance bias and detection bias) All outcomes | Low risk | Double‐dummy method |
Incomplete outcome data (attrition bias) Efficacy | Unclear risk | LOCF imputation |
Size Efficacy | Unclear risk | 50‐200 participants per treatment arm (76 to 144) |