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Comparison of Hemi-shoulder Arthroplasty and PHILOS in Treating Three or Four-part Fractures of Proximal Humerus

A Multi-center Study on Comparison of Hemi-shoulder Arthroplasty and PHILOS in Treating Three or Four-part Fractures of Proximal Humerus.

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03358784
Enrollment
300
Registered
2017-12-02
Start date
2018-03-05
Completion date
2019-03-01
Last updated
2017-12-02

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

Conditions

Humeral Fracture, Proximal

Keywords

Humeral Fractures, Proximal, Arthroplasty, Shoulder Replacement, Bone Plates

Brief summary

To explore clinical effectiveness of PHILOS plate fixation and hemi-shoulder arthroplasty in treating three or four-part fractures of proximal humerus

Detailed description

From April 2015 and April 2017, patients from multi-center aged over 60 years old with three and four-part fractures of proximal humerus were treated with Proximal Humerus Internal Locking System(PHILOS) and hemi-shoulder arthroplasty in multi-center. All the patients received the same rehabilitation course. At 6 months after surgery, postoperative complications were observed, EQ-5D was used to evaluate quality of life, and ASES score was used to assess functional outcomes.

Interventions

PROCEDUREHemi-shoulder Arthroplasty

Hemi-shoulder Arthroplasty treating three or four-part fractures of proximal humerus

PROCEDUREPHILOS Plate

PHILOS plate treating three or four-part fractures of proximal humerus

Sponsors

Peking University People's Hospital
Lead SponsorOTHER

Study design

Observational model
OTHER
Time perspective
CROSS_SECTIONAL

Eligibility

Sex/Gender
ALL
Age
60 Years to 85 Years

Inclusion criteria

three or four part fractures of proximal humerus

Exclusion criteria

1. Severe comminuted fractures of proximal humerus 2. past history of injured-side shoulder surgery 3. Patients who cannot tolerate surgery

Design outcomes

Primary

MeasureTime frameDescription
Postoperative complications6 months after surgeryPostoperative complications were observed

Secondary

MeasureTime frameDescription
EQ-5D6 months after surgeryEQ-5D was used to evaluate quality of life
ASES score6 months after surgeryASES was used to assess functional outcomes

Contacts

Primary ContactYichong Zhang, MD
875274428@qq.com15210802766

Outcome results

None listed

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