In women with osteoporosis, teriparatide reduced the relative risk of moderate or severe back pain risk by 31% versus placebo.
In plain wordsIn women with osteoporosis, teriparatide reduced moderate or severe back pain versus placebo.
- Peptide
- Teriparatide (PTH 1-34)
- Outcome
- DecreaseModerate or severe back pain
- Study
n = 1,085
- Comparator
- Placebo
- Analysis
- Secondary
- Outcome group
- Pain · Musculoskeletal
- Studied dose
- 20 microg · median 19 monthsAs given in this study (human).
Measurements
- Relative risk reduction
- 31%
- moderate or severe back pain, teriparatide versus placebo
- Incidence
- 16.5%
- moderate or severe back pain, placebo group
- Incidence
- 11.5%
- moderate or severe back pain, teriparatide 20 microg group
Source sentences
Women randomized to teriparatide 20 microg had a 31% reduced relative risk of moderate or severe back pain (16.5% vs. 11.5%, P = 0.016) and a 57% reduced risk of severe back pain (5.2% vs. 2.2%, P = 0.011).
2 context sentences(design, population, supporting numbers)
The risk of developing back pain was assessed following treatment with teriparatide [rh(PTH 1-34)] in postmenopausal women with osteoporosis.
postmenopausal women with prevalent vertebral fractures were administered teriparatide 20 microg (n = 541) or placebo (n = 544) for a median of 19 months.