Relative reduction of fracture risk for active treatment vs. placeboAbsolute reduction of fracture risk for active treatment (NNT)
TrialInclusion criteria (number of patients in the trial)DosageVertebral fracturesNonvertebral fracturesVertebral fracturesNonvertebral fractures
Risedronate (Actonel)
VERT19 Two or more vertebral fractures or one vertebral fracture and a T-score of −2.0 or lower (2,458)5 mg per day65% reduction after 1 year (P < .001)NR4% reduction after 1 year (25)NR
41% reduction after 3 years (P = .003)39% reduction after 3 years (P = .02)5% reduction after 3 years (20)3.2% reduction after 3 years (31)
VERT21 Two or more vertebral fractures (1,226)5 mg per day61% reduction after 1 year (P = .001)NR7.4% reduction after 1 year (14)NR
49% reduction after 3 years (P < .001)33% reduction after 3 years (P = .06)10.9% reduction after 3 years (9)5.1% reduction after 3 years (20)
HIP20 Osteoporosis or one or more risk factors for osteoporosis (9,331)2.5 and 5 mg per dayNR20% reduction after 3 years (P = .03)NR1.8% reduction after 3 years(56)
Alendronate (Fosamax)
 FIT22 Low femoral-neck BMD (4,432)5 mg per day for 2 years followed by 10 mg per day for 2 years44% reduction after 4 years (P = .001)12% reduction after 4 years (P = .13)1.7% reduction after 4 years (59)1.5% reduction after 4 years (67)
FIT23 Low femoral-neck BMD plus one or more clinical vertebral fractures (2,027)5 mg per day for 2 years followed by 10 mg per day for 1 year47% reduction after 3 years (P < .001)20% reduction after 3 years (P = .063)7% reduction after 3 years (14)2.8% reduction after 3 years (36)
Alendronate Phase III Osteoporosis Treatment Study31 Osteoporosis (994)5 or 10 mg per day for 3 years 20 mg per day for two years followed by 5 mg per day for 1 year48% reduction after 3 years, based on pooling of all data (P = .03)21% reduction after 3 years (P values not reported; not significant)3% reduction after 3 years (33)2.2% reduction after 3 years (45)