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Sponsors and Collaborators: |
Odense University Hospital National Board of Health, Denmark University of Southern Denmark Merck |
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Information provided by: | Odense University Hospital |
ClinicalTrials.gov Identifier: | NCT00414830 |
The purpose of this study is to determine if prevention of further fractures is possible through systematic evaluation for osteoporosis in patients with recent hip fracture
Condition |
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Hip Fracture Osteoporosis |
Study Type: | Observational |
Study Design: | Prospective |
Estimated Enrollment: | 600 |
Study Start Date: | January 2005 |
Estimated Study Completion Date: | September 2009 |
Osteoporosis is a common disease characterized by an increased risk of fracture. Furthermore recent studies has revealed that patients with fractures have increased risk of renewed fracture. Most fractures in the elderly are partly attributable to osteoporosis. The most severe of these shown to be the hip fracture (HFx) which increase mortality and decrease health related quality of life and has major impact on the level of national health service. Solid evidence is available showing several interventions to reduce the risk of osteoporotic fractures. In spite of this only few HFx patients are offered examination or treatment for osteoporosis and very rare this happens on a routine basis.
In the county of Funen and Ribe in Denmark the departments of Endocrinology and Orthopedic Surgery at Odense University Hospital and Hospital of South Western Jutland therefore initiated a fracture discharge program as part of a health technology assessment (HTA) study offering evaluation for osteoporosis to HFx patients. Evaluation consists of Duel Energy X-ray Absorptiometry, Instant Vertebral Assessment, a biochemical panel, and clinical assessment followed by specific anti-osteoporotic treatment as appropriate.
The HTA study is designed as a longitudinal cohort study of patients admitted to the participating departments with a low energy HFx. Inclusion started January first 2005 and ends December 31. 2006. After the last inclusion the follow up of the last patient are set to 2 years. In the study period data will be collected on subsequent fractures, epidemiological and demographic factors, questionnaires on quality of life, and register data on mortality, use of medication, and use of health services. The control group consists of patients admitted to any other hospital in the two participating counties who are not given this systematic evaluation for osteoporosis on a routine basis.
The HTA report will provide data to suggest if a systematic offer of evaluation and treatment of osteoporosis in HFx patients:
can reduce further fractures is accepted by the majority of patients can increase the amount of life years by decreasing mortality can increase quality of life by reducing the amount of fractures is cost effective for the health care providers
Ages Eligible for Study: | 45 Years and older |
Genders Eligible for Study: | Both |
Accepts Healthy Volunteers: | No |
Inclusion Criteria:
Exclusion Criteria:
Denmark | |
Odense University Hospital, Department og Endocrinology | |
Odense, Denmark, 5000 |
Principal Investigator: | Kim T Brixen, M.D.,PH.D. | Odense University Hospital |
Study ID Numbers: | 023 |
Study First Received: | December 21, 2006 |
Last Updated: | April 29, 2008 |
ClinicalTrials.gov Identifier: | NCT00414830 |
Health Authority: | Denmark: Danish Dataprotection Agency |
prevention health technology assessment population based fracture |
Hip Fractures Femoral Fractures Musculoskeletal Diseases Fractures, Bone Wounds and Injuries |
Disorders of Environmental Origin Osteoporosis Bone Diseases, Metabolic Leg Injuries Bone Diseases |
Hip Injuries |