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Clinical Trials/NCT02835053
NCT02835053
Completed
N/A

Frailty and Postoperative Outcomes After Emergency General Surgery

Ottawa Hospital Research Institute1 site in 1 country150,000 target enrollmentApril 2002

Overview

Phase
N/A
Intervention
Not specified
Conditions
General Surgery
Sponsor
Ottawa Hospital Research Institute
Enrollment
150000
Locations
1
Primary Endpoint
Mortality
Status
Completed
Last Updated
9 years ago

Overview

Brief Summary

The investigators will examine the association between preoperative frailty and postoperative outcomes and resource utilization after emergency general surgery.

Registry
clinicaltrials.gov
Start Date
April 2002
End Date
March 2014
Last Updated
9 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • All residents of Ontario aged more than 65 years on their surgery date with valid provincial health insurance who have an emergency general surgery procedure (large bowel surgery, small bowel surgery, cholecystectomy, control of hemorrhage from duodenal ulcer, lysis of adhesions, appendectomy, laparotomy)

Exclusion Criteria

  • No valid provincial health insurance

Outcomes

Primary Outcomes

Mortality

Time Frame: 365 days (from date of surgery)

Mortality events will be identified from the registered person's database in Ontario from the date of surgery to 365 days after surgery, at which time participants will be censored

Secondary Outcomes

  • Hospital length of stay(day of surgery to 365 days after surgery)
  • Intensive care unit admission(from date of surgery to 30 days after surgery)
  • Institutional discharge(Date of surgery to hospital discharge or 365 days after surgery (at which time participants will be censored))
  • Costs(day of surgery to 365 days after surgery)

Study Sites (1)

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