Efficacy of Japanese osteoporosis liaison service for secondary fracture prevention

Efficacy of Japanese osteoporosis liaison service for secondary fracture prevention - JOLS study

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

JPRN

Registry ID

JPRN-UMIN000032892

Enrollment

1400

Registered

2018-06-06

Start date

2018-06-01

Completion date

Unknown

Last updated

2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Osteoporosis

Interventions

Osteoporosis liaison service within 3 months after the fracture. In addition, the researchers remind the patients of the importance of the treatment at 6, 12 and 24 months after the fracture.

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: 1. Postmenopausal women or male equal to or over 50 years old 2. Primary osteoporosis 3. Admission in hospital due to new clinical vertebral fracture or hip fracture

Exclusion criteria

Exclusion criteria: 1. Bone metabolic diseases including primary hyperparathyroidism 2. Patients on hemodialysis and after kidney transplantation 3.Unwillingness to participate the study 4. Inappropriate patients due to clinical information

Design outcomes

Primary

Measure	Time frame
Clinical fragile fracture during 24 months after osteoporotic fracture	—

Countries

Japan

Contacts

Public ContactAtsushi Suzukui

Fujita Health University Department of Endocrinology and Metabolism

aslapin@fujita-hu.ac.jp0562939242

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026