Predictive Model for Postoperative Complications in Hemi-hip Arthroplasty

Complication Clinical Trial

Official title:

Predictive Model for Postoperative Complications in Elderly Patients With Hip Arthroplasty: Retrospective Study

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT03375268
• Other study ID #: 2017-10-003
• Status: Recruiting
• Phase: N/A
• First received: December 12, 2017
• Last updated: December 12, 2017
• Start date: January 1, 2011
• Est. completion date: August 31, 2018

Study information

• Verified date: December 2017
• Source: Seoul National University Hospital
• Contact: Eunsu Choi, pf
• Phone: 821032990658
• Email: potterydoll[@]hanmail.net
• Is FDA regulated: No
• Study type: Observational

Clinical Trial Summary

The purpose of this study was to identify the major complications and their risk factors of elderly patients who had undergone Hemi-hip Arthroplasty.

Description:

We retrospectively reviewed the medical records and reviewed the major complications and identify risk factors of elderly patients who had undergone Hemi-hip Arthroplasty for adults aged 60 years or older from January 2011 to December 2015.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 460
• Est. completion date: August 31, 2018
• Est. primary completion date: December 31, 2015
• Accepts healthy volunteers: No
• Gender: All
• Age group: 60 Years and older

Eligibility

Inclusion Criteria:

• A patient scheduled to undergo spinal anesthesia for Hemi-hip Arthroplasty

Exclusion Criteria:

• 1) Patients with acute infectious disease before surgery 2) Patients with fractures around the implant 3) Patients who underwent reoperation during hospitalization 4) During the study period, Duplicate patient who underwent the opposite side of the hip during hospitalization

Related Conditions & MeSH terms

• Arthroplasty
• Complication
• Elderly Patient
• Postoperative Complications
• Risk Factor

Locations

Country	Name	City	State
Korea, Republic of	Eulji university hospital	Seoul

Sponsors (1)

Lead Sponsor	Collaborator
Seoul National University Hospital

Country where clinical trial is conducted

Korea, Republic of, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	postoperative complications	we collect postoperative complications which include cardiac, pulmonary renal, cerebral, and other complications.	from operation day to postoperative 30 days