- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02848924
Current Incidence and Treatments Performed of Fractures of the Acetabulum and Pelvis in France in 2013 (ACETABULUM)
Study Overview
Detailed Description
Fractures of the acetabulum and pelvis are serious injuries to vital prognostic can play in cases of severe bleeding. In all cases the functional is a major issue with a potential reach of walking ability and maintaining the seated and standing positions. The treatment of such lesions requires management to a specialist, or the ability to use such centers for advice or transferring patients. This organization was recommended after the symposium of the French Society of Orthopedic Surgery (SOFCOT) in 2009. With the aging population, the incidence and clinical features of these fractures have evolved to worsening the functional prognosis. Club Basin acetabulum, body SOFCOT, wants to achieve an observational study assessing needs and practices at national and regional level. The long-term objective is to propose a regional organization of care of these patients in order to reduce morbidity and mortality associated.
FORMAT OF RESEARCH retrospective observational study of SNIIRAM data on hospitalizations for broken pelvis and acetabulum (CCAM codes S32.40 / S32.41 / S32.30 / S32.31 / S32.10 / S32.11 / S32.50 / S32 .51 / S32.70 / S32.71 / S32.80 / S32.81), with collection of the following data:
- Patient demographics: age, sex, comorbidities (DRG coding), place of residence.
- Length of hospital stay
- Treatment undertaken: CCAM coding during hospitalization
- Mortality at 30 days and 1 year.
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
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Ile-de-France
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Paris, Ile-de-France, France, 75014
- Groupe Hospitalier Paris Saint Joseph
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- All patients
Exclusion Criteria:
- No exclusion criteria
Study Plan
How is the study designed?
Design Details
- Observational Models: Cohort
- Time Perspectives: Retrospective
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Assessment of hospital stay length from medical file
Time Frame: Day 1 after hospitalization
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Day 1 after hospitalization
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|
Assesment of change of mortality
Time Frame: Day 30 and 1 year after hospitalization
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Assesment of change of mortality in this point time using a phone call.
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Day 30 and 1 year after hospitalization
|
Collaborators and Investigators
Investigators
- Principal Investigator: JOUFFROY Pommes, MD, Groupe Hospitalier Paris Saint Joseph
Study record dates
Study Major Dates
Study Start
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- ACETABULUM
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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