Outcomes of Severe Osteoporotic Fractures Hospitalized in France: the CROSS Cohort

Assistance Publique - Hôpitaux de Paris

Status: Completed

Conditions: Severe Fragility Fracture

Study type: Observational

Funder types: Other

Identifiers

NCT02606162

2014-A01371-46 (Other Identifier)

NI 13018

Details and patient eligibility

About

The purpose of this study is to determine the outcomes of severe osteoporotic fractures hospitalized in France, the risk of incident severe fracture at 2 years and 5 years and the risk of mortality over 2 and 5 years.

Full description

In France, the burden of osteoporotic fractures has been studied using cross sectional data from the French hospital national database. The availability of fracture liaison service in the main French cities allows the recruitment of a high number of these targeted patients. A large national multicenter, longitudinal, prospective cohort of patients hospitalized for severe osteoporotic fracture, the CROSS cohort ("Cohorte sur les Risques d'une OStéoporose Sévère"), in order to update data on prognosis (refracture, mortality), epidemiology and of severe osteoporotic fractures.

Enrollment: 912 patients

Sex: All

Ages: 60+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Men and women aged above 60 years, living in France and hospitalized for severe fragility fractures in response to low-energy trauma (e.g., a fall from standing height).
• Vertebral fractures have to be confirmed by an X ray examination.
• To be eligible for the study the patient has to be included and interviewed within 12 weeks of the fracture event's diagnosis. Note : patients in guardianship or curatorship can be included in this protocol.
• Informed and free consent given and form signed and dated

Exclusion criteria

• Non severe fracture (for example wrist fracture), pathological fractures, high trauma fractures and per prosthetic fractures.
• Non registration with a social security scheme (holder or beneficiary).