N/A
N=255
Analysis of the Relationship Between Early Postoperative Anemia and the Evolution of Autonomy at 6 Months in Patients 75 Years of Age and Older Operated on Following a Fracture of the Upper End of the Femur
Femoral Fracture
Bottom Line
View on ClinicalTrials.gov: NCT03810092 ↗Enrolled (actual)
255
Serious AEs
0.0%
Results posted
Sep 2025
Primary outcome: Primary: Hemoglobin Rate — 10 g/dl
Study Design & Population
- Study type
- Observational
- Phase
- N/A
- Interventions
- —
- Age
- Older Adult · 75+ yrs
- Sex
- All
- Sponsor
- Centre Hospitalier Departemental Vendee
- Primary completion
- Apr 2023
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Hemoglobin Rate |
10 | — |
| PRIMARY Questionnaire Activities of Daily Living |
1 | 0.05 |
Summary
Fracture of the upper extremity of the femur is a condition whose frequency increases with age. It is a serious disease, with multiple consequences such as a decrease in life expectancy, quality of life and patient autonomy. In this observational study, the investigators wish to evaluate the evolution of the autonomy of very elderly patients operated on for an upper extremity femur fracture as a function of early post-operative anemia.
Eligibility Criteria
Inclusion Criteria
- Age ≥ 75 years
- Patient operated on a fracture of the upper extremity of the femur
- Patient, family or close relative who does not object to participation in the study
- Patient affiliated to a social security system
- Patient who can be monitored as part of the protocol
Exclusion Criteria
- Refusal to participate in the study (patient, family or trusted relative)
- Patient with support on the operated limb not authorized by the surgeon
- Patient with an associated fracture (polytrauma, concomitant trauma to the upper limb...)
- Patient with a pathologic fracture
- Patient included in Category 1 interventional research (involving a drug or medical device)
- Patient deprived of liberty
- Patient not affiliated to a social security system
Data sourced from ClinicalTrials.gov (NCT03810092). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.