Baseline | follow‐up 7 weeks | follow‐up 15 weeks | follow‐up 27 weeks | ||||
Benefits: PAIN during walking activities |
PAIN during walking activities | PAIN during walking activities | PAIN during walking activities | Harms | |||
dosage group | VAS pain median (range) | VAS pain median change (range) | VAS pain median change (range) | VAS pain median change (range) | General pain (% improvement at 27 weeks) | Adverse events | |
1ml | N = 7 | 43 (7 to 71) | 7 (35 to 21) | 1 (58 to 22) | 6 (22 to 22) | 0% | 14% (1 patient reported mild to moderate pain) |
2ml | N = 7 | 81 (46 to 100) | 9 (−65 to 13) | 7 (97 to 19) | 7 (71 to 19) | 0% | 57% (4 patients reported mild to moderate pain) |
3ml | N = 6 | 48 (24 to 87) | 6 (39 to 10) | 7 (41 to 2) | 7 (87 to 17) | 0% | 17% (1 patient reported mild to moderate pain) |
3x1ml | N = 6 | 61 (16 to 88) | 29 (−78 to 7) | 47 (78 to 26) | 30 (78 to 26) | 67% | 17% (1 patient experienced severe pain) |