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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03971851
Other study ID # FrailtyAndSurgery
Secondary ID
Status Completed
Phase
First received
Last updated
Start date January 1, 2005
Est. completion date April 1, 2020

Study information

Verified date November 2019
Source University of Iceland
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

This study will validate the utility of a novel frailty index that uses ICD diagnoses to call frailty severity in a surgical cohort of patients 65 and older


Recruitment information / eligibility

Status Completed
Enrollment 50000
Est. completion date April 1, 2020
Est. primary completion date March 1, 2020
Accepts healthy volunteers No
Gender All
Age group 65 Years and older
Eligibility Inclusion Criteria: - Patients 65 years or older, undergoing any surgery at Landspitali University Hospital with an anesthesia team involved Exclusion Criteria: - No American Society of Anesthesiology classification provided

Study Design


Intervention

Other:
Frailty risk groups
Patients older than 65 will be separated into groups of varying frailty risk

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
University of Iceland

Outcome

Type Measure Description Time frame Safety issue
Primary 30-day mortality Mortality within 30 days of surgery in each of the three frailty risk groups 30-days
Primary Time to hospital readmission For patients surviving index hospitalization, the proportional hazard ratio of readmission between the three frailty group Up to 180 days
Secondary Long-term mortality Long-term mortality of the three different frailty risk groups, compared with proportional hazard modeling Up to 14 years
Secondary Prolonged hospital length-of stay Incidence of patients staying more than 10-days after surgery in the three frailty risk cohorts 3 months
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