Clinical Trials Logo

Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT03358784
Other study ID # PUPH2017PHF
Secondary ID
Status Not yet recruiting
Phase N/A
First received November 26, 2017
Last updated November 26, 2017
Start date March 5, 2018
Est. completion date March 1, 2019

Study information

Verified date November 2017
Source Peking University People's Hospital
Contact Yichong Zhang, MD
Phone 15210802766
Email 875274428@qq.com
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

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


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.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 300
Est. completion date March 1, 2019
Est. primary completion date March 1, 2019
Accepts healthy volunteers
Gender All
Age group 60 Years to 85 Years
Eligibility 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

Study Design


Intervention

Procedure:
Hemi-shoulder Arthroplasty
Hemi-shoulder Arthroplasty treating three or four-part fractures of proximal humerus
PHILOS Plate
PHILOS plate treating three or four-part fractures of proximal humerus

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Peking University People's Hospital

Outcome

Type Measure Description Time frame Safety issue
Primary Postoperative complications Postoperative complications were observed 6 months after surgery
Secondary EQ-5D EQ-5D was used to evaluate quality of life 6 months after surgery
Secondary ASES score ASES was used to assess functional outcomes 6 months after surgery
See also
  Status Clinical Trial Phase
Completed NCT03383991 - Reverse Total Shoulder Arthroplasty Versus Hemiarthroplasty for Displaced 3- and 4-part Proximal Humeral Fractures N/A
Completed NCT03023956 - Outcome of Proximal Humerus Fractures :Anatomic Neck Fractures vs Surgical Neck Fractures N/A
Completed NCT04821180 - Psychological Health Influences the Choice of Device in Proximal Humeral Fractures
Recruiting NCT04113044 - Go Fit Fast, Recovery Trajectory Using PROMIS®, Linking PROMIS®