ClinicalTrials.Veeva

Menu

Perioperative Complications in Reversed Shoulder Arthroplasties

F

Fundació Institut de Recerca de l'Hospital de la Santa Creu i Sant Pau

Status

Unknown

Conditions

Proximal Humeral Fracture

Study type

Observational

Funder types

Other

Identifiers

NCT03243409
IIBSP-HUM-2017-51

Details and patient eligibility

About

Retrospective observational study of reversed shoulder arthroplasties by proximal humeral fracture. Analysis of preoperative risk factors as well as minor and major complications at the first week, 90 days and 1 year.

Full description

The study is a multicenter retrospective observational study (3 centers). Data are collected from 105 patients over 65 years-old undergoing reversed shoulder arthroplasties by proximal humerus fractures, in 3 or 4 parts.

Patient information is obtained from the clinical records in their usual preoperative assessment, and follow-up on the usual routine checks, at the first week, 90 days and 1 year.

Minor and major complications rates are evaluated according to preoperative risk (ASA), underlying diseases and according to anticoagulant / antiaggregant treatments.

Likewise, transfusion rates related to ASA, as well as length of hospital stay related to it.

Enrollment

105 estimated patients

Sex

All

Ages

65+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Complex( 3- or 4-part) humerus fractures undergoing reversed shoulder arthroplasties.

Exclusion criteria

  • No exclusion criteria

Trial contacts and locations

1

Loading...

Central trial contact

Laura Noguera Alonso

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2025 Veeva Systems