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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02407873
Other study ID # 2013001
Secondary ID
Status Completed
Phase N/A
First received January 8, 2014
Last updated October 17, 2017
Start date February 2014
Est. completion date August 2017

Study information

Verified date October 2015
Source University Hospital of Liege
Contact n/a
Is FDA regulated No
Health authority
Study type Observational [Patient Registry]

Clinical Trial Summary

The score on the Edmonton frail scale will be recorded in 250 consecutive patient aged of 75 years or more and undergoing elective cardiac surgery. In those patients the investigators will also record the ITU length of stay, the hospital length of stay, the incidence of complications, the ability to be discharged home and to live independently at postoperative day 30.

The ability of the Edmonton score to predict complication, prolonged hospital and ITU length of stay as well as loss of autonomy at discharge and day 30 will be assessed.


Recruitment information / eligibility

Status Completed
Enrollment 254
Est. completion date August 2017
Est. primary completion date June 2017
Accepts healthy volunteers No
Gender All
Age group 75 Years and older
Eligibility Inclusion Criteria:

- 75 yo and older

- Elective cardiac surgery

Exclusion Criteria:

- Refuse or inability to give consent

- Emergency surgery

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Non


Locations

Country Name City State
Belgium CHU of Liege Liege

Sponsors (1)

Lead Sponsor Collaborator
University Hospital of Liege

Country where clinical trial is conducted

Belgium, 

Outcome

Type Measure Description Time frame Safety issue
Primary 30-day mortality 30 Days
Secondary Loss of autonomy at discharge (Edmonton score) 30 Days
Secondary Loss of autonomy at day 30 (Edmonton score) 30 days
Secondary Incidence of predefined complications 30 Days
Secondary Length of hospital stay 30 days
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