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Femoral frACturEs and COVID-19.

Femoral frACturEs and COVID-19. Retrospective Comparative Cohort Study on the Early Prognosis of Patients Affected by Proximal Femur Fractures and COVID-19.

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04657510
Acronym
FACE COVID-19
Enrollment
140
Registered
2020-12-08
Start date
2020-11-14
Completion date
2020-12-31
Last updated
2020-12-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Covid19, Femur Fracture, Fragility Fracture

Keywords

proximal femur fracture, fragility fracture, Covid-19, SARS-CoV2, FACE-COVID 19, prognosis, cohort study

Brief summary

Retrospective cohort study comparing the early prognosis after surgically-treated proximal femur fragility fractures in patients affected and not affected by COVID-19.

Interventions

OTHERCOVID-19

Patients affected versus not affected by COVID-19, with the same starting condition (proximal femur fracture)

Sponsors

I.R.C.C.S Ospedale Galeazzi-Sant'Ambrogio
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
45 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Age ≥45 years * Admitted to IRCCS Orthopaedic Institute Galeazzi for proximal femur fractures from march 2020 to april 2020. * Tested for COVID-19 through naso-pharyngeal swab analized with RT-PCR

Exclusion criteria

* Age \<45 years * Not tested for SARS-CoV-2 * Other fractures (including bilateral proximal femur fractures)

Design outcomes

Primary

MeasureTime frameDescription
Survival at discharge day (comparison between the two groups)on discharge day, on average after 1 weekSurvival at discharge day (comparison between the two groups)

Secondary

MeasureTime frameDescription
Length of stay (comparison between the two groups)on discharge day, on average 1 weekLength of stay (comparison between the two groups)
Readmission rate (comparison between the two groups)up to 30 days after dischargeReadmission rate (comparison between the two groups)
Complications rate (comparison between the two groups)up to 30 days after dischargeComplications rate (comparison between the two groups)
Survival at 30 days after discharge (comparison between the two groups)30 days after dischargeSurvival at 30 days after discharge (comparison between the two groups)
Routine lab exams values (comparison between the two groups)At admission, 1st postoperative day, 5th postoperative day, on discharge dayRoutine lab exams values (comparison between the two groups)

Countries

Italy

Contacts

Primary ContactGiuseppe M Peretti, MD
giuseppe.peretti@unimi.it0039 3396610282

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026