Table 1.
Characteristics of studies
Study
|
Condition
|
Duration (weeks)
|
Celecoxib treatment
|
Comparator treatment#
|
|||
---|---|---|---|---|---|---|---|
No. of subjects | Total daily dose (mg) | Dosing regime | No. of subjects | Treatment | |||
Solomon et al. (Ref 6) | P | 145-161 | 1356 | 400 800 | BD | 679 | Pl |
CLASS (White et al., Ref 12)* | OA/RA | 52 | 3987 | 800 | BD | 3981 | lb, Di |
Pfizer (Ref 15) | AD | 52 | 285 | 400 | BD | 140 | Pl |
McKenna et al. (Ref 16) | OA | 6 | 201 | 200 | BD | 399 | Pl, Di |
PreSAP (Levin, Ref 17) | P | 156 | 933 | 800 | OD | 628 | Pl |
Geba et al. (Ref 18) | OA | 6 | 97 | 200 | OD | 94 | Para |
RA, rheumatoid arthritis; OA, osteoarthritis; AD, Alzheimer's disease; P, prevention of colorectal adenoma in high risk subjects; lb, ibuprofen; Di, diclofenac; Pl, placebo; Para, paracetamol; CV, cardiovascular; OD, once daily; BD, twice daily; PreSAP, Prevention of Colorectal Sporadic Adenomatous Polyps
For the CLASS (Celecoxib Long-term Arthritis Safety Study) trial, the findings documented in White et al. (Ref 12) were used in the meta-analysis