Table 9.
Study: CRPS Type I Criteria | Treatment | Results | Comment | Adverse Effects |
---|---|---|---|---|
Manicourt et al, Budapest criteria; P, R, PC, DB, C | Alendronate, 40 mg orally daily x 8w vs placebo; 40 patients, 20 per group | Alendronate significantly better | Patients who continued to the open-label phase had new or dramatic improvement | Upper gastrointestinal intolerance |
Van de Vusse et al; IASP criteria; P, R, DB, PC, C | Gabapentin x 3w, titrated to 600 mg TID vs placebo, 2w washout, then 3w of crossover treatment; 58 patients, 29 per group | Significantly better pain relief with gabapentin during treatment, less in second period (washout), no significant effect when both periods were combined | Sensory deficit significantly reversed with gabapentin. | Dizziness, somnolence, lethargy |
Groeneweg et al, Budapest criteria; P, R, PC | Tadalafil, 10 mg for 4w then 20 mg for another 84 vs placebo; 24 patients, 12 per group | Non-statistically significant change in temperature; statistically and clinically relevant decrease in pain with tadalafil | No difference in muscle strength between groups; interventions did not improve activity levels. | None |
C: Crossover; DB: Double-blind; IASP: International Association for the Study of Pain; P: Prospective; R: Randomized