Skip to main content
. 2025 Feb 13;483(7):1264–1271. doi: 10.1097/CORR.0000000000003415

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.

a

Mostly subjective because nerve conduction studies confirming neuropathy were optional.

b

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.