Comparison of ASA and CFS in Anesthesiology
CACA
Comparison of ASA and CFS in Predicting Peri- and Postoperative Outcomes in Elective Patients Older Than 65 Years
1 other identifier
observational
200
1 country
1
Brief Summary
In addition to the regular ASA classification, patients would also be assigned the Clinical frailty scale (CFS) during preoperative examinations in anesthesiology clinics. The aim is to compare the usefulness of ASA and CFS categorization for predicting perioperative and postoperative complications and length of postoperative stay in elective surgeries.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Jul 2023
Shorter than P25 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
July 17, 2023
CompletedFirst Submitted
Initial submission to the registry
August 11, 2023
CompletedFirst Posted
Study publicly available on registry
August 21, 2023
CompletedPrimary Completion
Last participant's last visit for primary outcome
April 30, 2024
CompletedStudy Completion
Last participant's last visit for all outcomes
June 3, 2024
CompletedAugust 21, 2023
August 1, 2023
10 months
August 11, 2023
August 11, 2023
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Peri- and postoperative complications
Peri- and postoperative complications depending on CFS and ASA
During 2 months after elective operation
Secondary Outcomes (1)
Length of stay in hospital
During 2 months after elective operation
Eligibility Criteria
Study population is all elective patients of the Osijek University Hospital older then 65 years who were included during the preoperative examination.
You may qualify if:
- All elective patients older then 65 years
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
University Hospital Centre Osijek
Osijek, 31000, Croatia
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- STUDY CHAIR
Slavica Kvolik, MD
Osijek University Hospital; Medical Faculty Osijek
Central Study Contacts
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- PROSPECTIVE
- Target Duration
- 2 Months
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
August 11, 2023
First Posted
August 21, 2023
Study Start
July 17, 2023
Primary Completion
April 30, 2024
Study Completion
June 3, 2024
Last Updated
August 21, 2023
Record last verified: 2023-08