3. Summary of treatments.
ATC group, trial | Substance | Daily dose | Maximum recommended dose | Treatment duration | Sample size calculation | Participants per group (n) |
Butylpyrazolidin | ||||||
Grevsten 1975 | Phenylbutazone (Butazolidin) IM day 1; phenylbutazone (Butazolidin Alka) orally day 2 to 4 | 0.6 g IM day 1, 0.6 g day 2 to 4 by mouth, 0.3 g day 5 to 14 | No longer approved for human use | 14 days | No | 36 |
Weber 1980 | Phenylbutazone (Butazolidin Alka) | 600 mg day 1 to 3, 300 mg day 4 to 5 | No longer approved for human use | 5 days | No | 59 |
Radin 1968 | Phenylbutazone | 600 mg day 1 to 2, 300 to 800 mg day 3 to 8 | No longer approved for human use | 8 days | No | 25 |
Acetic acid derivatives | ||||||
Goldie 1968a | Indomethacin | 75 mg | 225 mg | 14 days | No | 25 |
Herrmann 2009 | Diclofenac | 100 mg day 1 and 5; 150 mg day 2 to 4 | 150 to 200 mg | 4 days | 50 per group | 57 |
Dreiser 2001b | Diclofenac | 150 mg | 150 to 200 mg | 14 days | 150 per group | 162 |
Kanayama 2005 | Diclofenac vs active treatment | 75 mg | 150 to 200 mg | 14 days | 20 per group | 20 |
Oxicams | ||||||
Dreiser 2001a (placebo‐controlled trial) | Meloxicam 7.5/15 mg | 7.5/15 mg | 15 mg | 7 days | 150 per group | 171/181 |
Dreiser 2001b (diclofenac‐controlled trial) |
Meloxicam 7.5/15 mg | 7.5/15 mg | 15 mg | 14 days | 150 per group | 164/163 |
Weber 1993 | Piroxicam | 100 mg day 1 to 2, 20 mg day 3 to 14 | 20 mg | 14 days | No | 120 |
Herrmann 2009 | Lornoxicam | 24 mg day 1; 16 mg day 2 to 4; 8 mg day 5 | 16 mg | 5 days | 50 per group | 57 |
Propionic acid derivative | ||||||
Braun 1982 | Ketoprofen vs active treatment | 200 mg IM day 1 to 3, 300 mg orally + supp day 4 to 8 | 200 (max 300) mg | 9 days | No | 17 |
Fenamates, coxibs, or others | ||||||
No studies | ‐‐ | ‐‐ | ‐‐ | ‐‐ | ‐‐ | ‐‐ |
ATC: Anatomical Therapeutic Chemical IM: intramuscular