Trial | Design | Number R/C | Dose | Duration (wk) | Outcome* |
---|---|---|---|---|---|
Chad et al,36 1990 | R,DB,PL | 58/46 | 0.075% cap qid | 4 | Significant improvements |
VAS-R (71 vs 41%) | |||||
Not significant | |||||
VAS-P | |||||
PGE | |||||
Scheffler et al,32 1991 | R,DB,PL | 54/49 | 0.075% cap qid | 8 | Significant improvements |
PGE (90 vs 50%) | |||||
VAS-P (49 vs 17%) | |||||
VAS-R (66 vs 39%) | |||||
Capsaicin Study Group,37 | R,DB,PL | 277/219 | 0.075% cap qid | 8 | Significant improvements |
1991 | PGE (71 vs 51%) | ||||
VAS-P (40 vs 28%) | |||||
VAS-R (60 vs 45%) | |||||
Tandan et al,38 1992 | R,DB,PL | 22/20 | 0.075% cap qid | 8 | Significant improvements |
PGE (60 vs 20%) | |||||
Not significant | |||||
VAS-P | |||||
VAS-R | |||||
Low et al,39 1995† | R,DB,PL | 40/39 | 0.075% cap qid | 12 | Not significant |
PGE | |||||
VAS-P | |||||
VAS-R |
Note: R=randomized, DB=double-blind, PL = placebo-controlled, C=number of patients completing trial, VAS-R=visual analogue scale for pain relief, VAS-P=visual analogue scale for pain severity, PGE=physician’s global evaluation based on a rating scale of change in pain severity.
* Numbers in parenthesis indicate significant difference in favor of capsaicin compared with placebo.
† Only 12% of patients enrolled in this trial had diabetes.