Back to Search Start Over

Design of a randomized clinical trial of concurrent treatment with vitamin K2 and risedronate compared to risedronate alone in osteoporotic patients: Japanese Osteoporosis Intervention Trial-03 (JOINT-03)

Authors :
Nobuaki Miyakawa
Tatsuhiko Kuroda
Masataka Shiraki
Yasuo Ohashi
Satoshi Mori
Hiroshi Hagino
Shiro Tanaka
Eiji Itoi
Hiroaki Ohta
Takayuki Hosoi
Masao Fukunaga
Teruhiko Miyazaki
Toshitsugu Sugimoto
Hajime Orimo
Yukari Uemura
Toshitaka Nakamura
Source :
Journal of Bone and Mineral Metabolism. 32:298-304
Publication Year :
2013
Publisher :
Springer Science and Business Media LLC, 2013.

Abstract

Concurrent treatments with bisphosphonates and vitamin K are promising given that bisphosphonates possibly interfere with vitamin K activation. This is a prospective, multi-center, open-labeled, randomized trial of the efficacy of concurrent treatment with vitamin K2 and risedronate compared with risedronate alone and to explore subsets of patients for which concurrent treatment is particularly efficacious (trial identification number UMIN000000991). Inclusion criteria are women who meet the criteria for pharmacological therapy for osteoporosis, aged ≥65 years, have any of pre-specified risk factors, can walk unassisted, and are able to answer questionnaires. Exclusion criteria are prior warfarin use, secondary osteoporosis or non-osteoporotic metabolic bone diseases, contraindication for vitamin K2 and risedronate, hyper- or hypoparathyroidism, mental disorders, prevalent vertebral fracture at ≥6 sites, severe degenerative spinal deformation between T4 and L4, serious heart, liver, or kidney disease, or bisphosphonate use within the previous 6 months. Patients were recruited from 123 institutes between January 2008 and February 2010, and allocated to vitamin K2 (45 mg/day) and risedronate (2.5 mg/day or 17.5 mg/week) or risedronate alone (2.5 mg/day or 17.5 mg/week) groups. Primary endpoint is a vertebral or non-vertebral fracture. Secondary endpoints are bone mineral density, height, undercarboxylated osteocalcin, JOQOL, EQ-5D and safety. A sample size of 910 subjects per group and 2-year follow-up will provide 80 % power to detect 35 % risk reduction for fracture, with a two-sided significance level of 5 %. Subgroup analysis stratified to adjustment factors for random allocation, body mass index, 25-hydroxyvitamin D, estimated glomerular filtration rate, grade of vertebral fracture, JOQOL, EQ-5D, and co-morbidity is pre-specified.

Details

ISSN :
14355604 and 09148779
Volume :
32
Database :
OpenAIRE
Journal :
Journal of Bone and Mineral Metabolism
Accession number :
edsair.doi.dedup.....75e26064a59a3c268f20c21c5c2adbfb
Full Text :
https://doi.org/10.1007/s00774-013-0491-4