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

NCT ID: NCT03810092

Last Updated: 2025-09-19

Study Results

Results available

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Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

255 participants

Study Classification

OBSERVATIONAL

Study Start Date

2019-05-20

Study Completion Date

2023-04-12

Brief Summary

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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.

Detailed Description

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Conditions

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Femoral Fracture

Study Design

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Observational Model Type

OTHER

Study Time Perspective

PROSPECTIVE

Eligibility Criteria

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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
Minimum Eligible Age

75 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Centre Hospitalier Departemental Vendee

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Romain DECOURS

Role: PRINCIPAL_INVESTIGATOR

CHD Vendée

Locations

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CHU Angers

Angers, , France

Site Status

CH Cholet

Cholet, , France

Site Status

Centre Hospitalier Départemental Vendée

La Roche-sur-Yon, , France

Site Status

CH La Rochelle

La Rochelle, , France

Site Status

CH Saint Malo

St-Malo, , France

Site Status

Countries

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France

Provided Documents

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Document Type: Study Protocol and Statistical Analysis Plan

View Document

Other Identifiers

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CHD117-17

Identifier Type: -

Identifier Source: org_study_id

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