Table 1.
Study characteristics
| Author [ref]. | Study type | Drug studied | Drug dosage per day | Nerve injury diagnosis | Participants | Age in years | Women | |||
| Gabapentinoids | Placebo | Gabapentinoids | Placebo | Gabapentinoids | Placebo | |||||
| Markman et al. [21] | RCT | Pregabalin | 150 mg to 600 mg | Mostly subjective criteriaa | 51 (275) | 49 (267) | 53 ± 13 | 54 ± 13 | NR | NR |
| van Seventer et al. [33] | RCT | Pregabalin | 150 mg to 600 mg | Subjective criteria | 50 (127) | 50 (127) | 52 ± 14 | 51 ± 13 | 61 (77) | 41 (52) |
| Gordh et al. [10] | Quasi-RCT: crossoverb | Gabapentin | 300 mg to 2400 mg | Subjective criteria | 100 (98) | 100 (98) | 49 ± NR | 49 ± NR | 53 (52) | 53 (52) |
| Jenkins et al. [13] | Quasi-RCT: crossoverb | Pregabalin | 300 mg | Subjective criteria | 100 (25) | 100 (25) | 50 ± 14 | 50 ± 14 | 56 (14) | 56 (14) |
Data presented as % (n) or mean ± SD. NR = not reported.
Mostly subjective because nerve conduction studies confirming neuropathy were optional.
Patients were randomized to receive either gabapentinoids or placebo in the first period, followed by a washout period, then switched to the alternate treatment in the second period.