- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT00643175
Effectiveness of Automated Inpatient Endocrinology Consultation for Osteoporotic Hip Fracture
December 29, 2009 updated by: State University of New York - Upstate Medical University
Osteoporosis has been called a "silent epidemic" whose prevalence is increasing.
It often presents as a fragility fracture, with hospitalizations resulting from minimally traumatic hip fractures.
While the fractures are treated appropriately, the underlying pathology is often ignored.
Numerous studies have shown that prior fracture increases the risk for further fracture.
In 2004 the Surgeon General released a report on osteoporosis, the details of which include multi-disciplinary treatment of osteoporotic fractures.
Treatment of osteoporosis after hip fracture is also being targeted as a future hospital quality assessment measure.
Hospitals which have no plan in place to address osteoporosis treatment after hip fracture may be cited, and may have medicare money withheld.
The goal of the study is to create an automated in-patient endocrinology consultation for osteoporotic hip fractures.
We plan to gather patient data in a prospective manner including the endocrinologist recommendations, adherence to medical therapy after discharge, and future fracture rates.
Possible planned interventions include only appropriate medical therapy for osteoporosis, DEXA bone scanning, and regularly scheduled telephone follow-up.
Study Overview
Study Type
Observational
Enrollment (Anticipated)
20
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
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New York
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Syracuse, New York, United States, 13202
- SUNY Upstate Medical University
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-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
55 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
Using the existing WebCAIS order system, an automated endocrinology consult and appropriate laboratory studies will be drawn on all non-traumatic hip fractures.
Data from these patients will be collected in a prospective study, and the patients will be followed up over time to check adherence to osteoporotic medical therapy and future incidence of re-fracture.
Description
Inclusion:
- over 55
- non-traumatic hip fracture
Exclusion criteria:
- currently on anti-osteoporosis pharmacotherapy including bisphosphonates, PTH, and calcitonin
- high energy nature of fracture, including MVA, fall from height greater than 3 feet
- severe dementia, lack of capacity
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
1
Osteoporosis in patients with fragility hip fractures.
|
Treatment of osteoporosis after hip fracture is also being targeted as a future hospital quality assessment measure.
Hospitals which have no plan in place to address osteoporosis treatment after hip fracture may be cited, and may have medicare money withheld.
The goal of the study is to create an automated in-patient endocrinology consultation for osteoporotic hip fractures.
We plan to gather patient data in a prospective manner including the endocrinologist recommendations, adherence to medical therapy after discharge, and future fracture rates.
Planned interventions include only appropriate medical therapy for osteoporosis, DEXA bone scanning, and regularly scheduled telephone follow-up.
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
June 1, 2007
Primary Completion (Actual)
January 1, 2009
Study Completion (Actual)
January 1, 2009
Study Registration Dates
First Submitted
March 24, 2008
First Submitted That Met QC Criteria
March 25, 2008
First Posted (Estimate)
March 26, 2008
Study Record Updates
Last Update Posted (Estimate)
December 30, 2009
Last Update Submitted That Met QC Criteria
December 29, 2009
Last Verified
December 1, 2009
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- osteoporotic hip fracture
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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