DeFRA Questionnaire as an Anamnestic Form

Valmontone Hospital

Status: Completed

Conditions: Osteoporosis

Study type: Observational

Funder types: Other

Identifiers

NCT02003716

VDA-001-2012

Details and patient eligibility

About

The DeFRA questionnaire is a new validated algorithm derived from FRAX. Here we use the DeFRA as a "primary anamnestic from" to identify subjects at risk of osteoporosis in a population never screened before and never treated for this disease.

Full description

There is an increasing recognition that the management of osteoporosis requires the characterization of fracture risk to be based on absolute risk rather than single measures such as bone mineral density (BMD). However, the threshold for pharmacological intervention for osteoporosis remains controversial.

The aim of the present project is to perform a large scale study to identify subjects at risk of osteoporosis by administering the DeFRA questionnaire in a population never screened or treated before for osteoporosis.

DeFRA questionnaire will be administered before and after DEXA scanning, to further validate the questionnaire and to highlight the predictive value of this protocol as a tool to screen the general population.

Enrollment: 767 patients

Sex: Female

Ages: 50 to 70 years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• age: 50 to 70 years
• no overt pathologies
• never screened before for osteoporosis
• no prior use of drugs for osteoporosis
• signed informed consent form

Exclusion criteria

• overt pathologies (cancer, neurodegenerative diseases, renal or hepatic insufficiency)
• use of the following drugs: cortisones, loop diuretics, antiepileptic drugs, aromatase inhibitors, dicoumarols, thyroxin in suppressive therapy, antiosteoporosis drugs)
• patients who underwent radiation therapy
• hypercalcemia or alterations of the phospho-calcic metabolism
• patients with metabolic diseases of the bone (including hyperparathyroidism or Paget disease)

Trial design

767 participants in 1 patient group

No treatment