Proximal Femoral Fractures - Patient Population, Risk Factors, Surgical Performance and Outcome
NCT ID: NCT03768622
Last Updated: 2021-11-04
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
2906 participants
OBSERVATIONAL
2018-06-01
2021-03-06
Brief Summary
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This study analyses preexisting risk factors for proximal femoral fractures as well as for failing to reach the previous functional level, difference in outcome between patients with femoral neck fracture compared to those with pertrochanteric fracture, surgical performance and its significance for the functional outcome, as well as the impact of proximal femoral fractures on patients' one-year independence.
Detailed Description
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Conditions
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Keywords
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Study Design
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COHORT
RETROSPECTIVE
Study Groups
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surgery for femoral neck fracture
patients with proximal femoral fracture (type: femoral neck fracture) with surgical procedure: partial hip arthroplasty
surgery for femoral neck fracture
surgical treatment for proximal femoral fracture with a partial hip arthroplasty in case of femoral neck fractures
surgery for pertrochanteric femoral fractures
patients with proximal femoral fracture (type:pertrochanteric femoral fractures) with surgical procedure: intramedullary nail type Gamma® Nail or similar
surgery for pertrochanteric femoral fracture
surgical treatment for proximal femoral fracture with intramedullary nail type Gamma® Nail or similar in case of pertrochanteric fractures
Interventions
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surgery for pertrochanteric femoral fracture
surgical treatment for proximal femoral fracture with intramedullary nail type Gamma® Nail or similar in case of pertrochanteric fractures
surgery for femoral neck fracture
surgical treatment for proximal femoral fracture with a partial hip arthroplasty in case of femoral neck fractures
Eligibility Criteria
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Inclusion Criteria
* with a partial hip arthroplasty in case of femoral neck fractures
Exclusion Criteria
* Documented dissent in study participation
ALL
No
Sponsors
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University Hospital, Basel, Switzerland
OTHER
Responsible Party
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Principal Investigators
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Franziska Saxer, Dr. MD
Role: PRINCIPAL_INVESTIGATOR
Department of Orthopaedics and Trauma Surgery (DOTS).
Locations
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Department of Orthopaedics and Trauma Surgery (DOTS).
Basel, , Switzerland
Countries
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Other Identifiers
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2018-00933; ch18Saxer2
Identifier Type: -
Identifier Source: org_study_id