1. Study design of the 23 included trials.
Study |
Number of participants Study design Patient focus |
Mean age (yrs) |
Female | Male | F: M ratio |
Quinine dose (mg) |
Treatment period (d) |
Washout period (d) | Treatment comparisons |
BioDesign 1984a | n = 24 Study design = C Patient focus = I |
57 | 11 | 13 | 0.8 | 260 | 7 | 7 | Quinine‐vitamin E combination (Q‐Vel®)b ✓ |
Bottner 1984a | n = 69 Study design = C Patient focus = I |
51 | 66 | 3 | 22.0 | 260 | 14 | 14 | Placebo ✓ |
CIBA 1988a | n = 556 Study design = P Patient focus = I |
45 | 393 | 163 | 2.4 | 260 | 14 | n/a | Placebo ✓ Vitamin E ✓ Quinine‐vitamin E combination (Q‐Vel®) ✓ |
Connolly 1992 | n = 30 Study design = C Patient focus = I |
59 | 0 | 30 | 0.0 | 500 | 28 | 28 | Placebo ✓ Vitamin E ✓c |
Dunn 1993 | n = 28 Study design = C Patient focus = I |
67 | 17 | 11 | 1.5 | 300 | 30 | 3 | Placebo ✓ |
Diener 2002 | n = 94 Study design = P Patient focus = I |
49 | 66 | 32 | 2.1 | 400 | 14 | n/a | Placebo ✓ |
Fung 1989 | n = 9 Study design = C Patient focus = I |
63 | 7 | 1 | 7.0 | 200 | 28 | 7 | Placebo ✓ |
Gorlich 1991 | n = 164 Study design = P Patient focus = I |
56 | 119 | 45 | 2.6 | 260 | 14 | n/a | Placebo ✓ Quinine‐theophylline combination (Limptar®)b ✓ |
Hays 1986a | n = 62 Study design = C Patient focus = I |
47 | 49 | 13 | 3.8 | 325 | 14 | 14 | Placebo ✓ |
Jansen 1994 | n = 20 Study design = P Patient focus = I |
55 | 14 | 6 | 2.3 | 300 | 14 | n/a | Placebo ✓ |
Jansen 1997 | n = 106 Study design = P Patient focus = I |
51 | 68 | 44 | 1.5 | 300 | 14 | n/a | Placebo ✓ |
Jones 1983 | n = 9 Study design = C Patient focus = I |
_ | _ | _ | _ | 300 | 14 | 14 | Placebo ✓ |
Kaji 1976 | n = 9 Study design = C Patient focus = H |
_ | _ | _ | _ | 320d | 42d | 0 | Placebo ✓ |
Lee 1991 | n = 31 Study design = P Patient focus = L |
62 | 5 | 26 | 0.2 | 400 | 28 | n/a | Placebo ✓ |
Leo Winter 1986a | n = 205 Study design = C Patient focus = I |
44 | 173 | 32 | 5.4 | 260 | 5 | 2 | Placebo ✓ Vitamin E ✓ Quinine‐vitamin E combination (Q‐Vel®) ✓ |
Lim 1986 | n = 25 Study design = P Patient focus = I |
_ | _ | _ | _ | 300 | ≤ 14 | n/a | Placebo ✓ |
Maule 1990 | n = 16 Study design = C Patient focus = I |
76 | 10 | 6 | 1.7 | 300 | 21 | 0 | Placebo ✓ |
Prateepavanich 1999 | n = 24 Study design = P Patient focus = Ie |
64 | 21 | 3 | 7.0 | 300 | 28 | n/a | Xylocaine injection ✓ |
Roca 1992 | n = 30 Study design = P Patient focus = H |
48 | 10 | 19 | 0.5 | 325 | 60f | n/a | Vitamin E ✓ |
Sidorov 1993 | n = 19 Study design = C Patient focus = I |
58 | 14 | 2 | 7.0 | 200 | 14 | 14 | Placebo ✓ |
Smith 1985 | n = 21 Study design = C Patient focus = I |
73 | _ | _ | _ | 300 | 21 | 0 | Placebo ✓ |
Warburton 1987 | n = 22 Study design = C Patient focus = I |
74 | 16 | 6 | 2.7 | 300 | 21 | 0 | Placebo ✓ |
Woodfield 2005 | n = 13 Study design = N‐of‐1 Patient focus = I |
75 | 7 | 6 | 1.2 | 200 to 300 | 42 | 0 | Placebo ✓ |
Abbreviations: C: cross‐over, P: parallel, H: haemodialysis‐induced cramps, I: idiopathic, L: patients with liver cirrhosis; n/a: not available
aUnpublished. bQ‐Vel®: trade name for quinine‐vitamin E combination; Limptar®:trade name for quinine‐theophylline combination. cConnolly 1992 did not directly compare quinine versus vitamin E ‐ using the data provided we were able to draw comparison. dQuinine dose given at beginning of each dialysis session (3 times per wk) and not daily. eInclusion criteria included presence of myofascial trigger point in gastrocnemius. fA 60‐day trial but results only reported from first month of treatment.