Post-operative Anemia in Lateral Fractures of the Femur.

Status Completed

Clinical Trial Summary

It was conducted a prospective study with a series of 45 patients with lateral fragility fractures of the femur treated by three different intramedullary nails. Patients were randomized in Group A (15 patients treated by Affixus Zimmer-Biomet), Group B (15 patients treated by EBA2 - Citieffe) and Group C (15 patients treated by Proximal Femoral Nail Antirotation Synthes). One independent observer performed seven biochemical evaluations (hemoglobin serum value) from admission to patient discharge. Surgical time and Blood transfusions number were reported for each partecipant.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT05225753
Study type	Observational
Source	Azienda Ospedaliero-Universitaria Consorziale Policlinico di Bari
Contact
Status	Completed
Phase
Start date	November 1, 2020
Completion date	September 1, 2021

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See also
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