The Relationship Between the ASA Score Determined by Operating Room Nurses and Intubation Duration
1 other identifier
observational
80
1 country
1
Brief Summary
The objective of this study is to The objective of this study was to ascertain the extent to which operating room nurses assign ASA scores and to assess the reliability of these scores in predicting significant risk factors, including the necessity for mechanical ventilation in patients.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for all trials
Started Apr 2025
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
April 1, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
July 1, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
July 1, 2025
CompletedFirst Submitted
Initial submission to the registry
January 12, 2026
CompletedFirst Posted
Study publicly available on registry
February 3, 2026
CompletedFebruary 3, 2026
January 1, 2026
3 months
January 12, 2026
January 25, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (3)
Determining the sociodemographic information of the nurse using "Personal Information Form 1"
The nurse's assessment is a nine-item form that includes information such as age, gender, professional work experience, experience working in an operating room, work style, average weekly working hours, income level, and whether or not they have received ASA Physical Status Classification training.
From April 2025 to June 2025
Determining the sociodemographic information of anesthesiologists using "Personal Information Form 3"
This is an 8-item form that includes the anesthesiologist's age, gender, professional work experience, operating room experience, work style, average weekly working hours, income level, and whether they have received ASA Physical Status Classification training.
From April 2025 to June 2025
Determining the sociodemographic information of the patient's using "Personal Information Form 3"
This is an 8-item form that includes the patient's age, gender, chronic diseases, previous surgical procedures, Glasgow Coma Scale score, ASA class score, need for mechanical ventilation, and number of days the patient has been intubated.
From April 2025 to June 2025
Secondary Outcomes (1)
Comparing patients' ASA scores with their need for mechanical ventilation
From April 2025 to June 2025
Study Arms (1)
1
Inclusion Criteria for Volunteers in the Study: * The person must be 18 years of age or older, * The person must be willing to participate in the study. Exclusion Criteria for Volunteers in the Study: * The person must be 18 years of age or younger, * The person must not be a volunteer to participate in the study, * The person must be classified as ASA VI, * The person must have died during surgery.
Eligibility Criteria
This study was conducted at Zonguldak Atatürk State Hospital between 1 April and 1 July 2025. The operating room was staffed by 36 nurses, 12 anesthesiologists (across 12 operating tables) and 80 patients. A review of extant research on the subject was conducted, and a G Power analysis was subsequently performed. This analysis indicated that, in order to achieve 80% power within a 95% confidence interval for an effect size of d=0.8, it is necessary to include 80 individuals meeting the inclusion criteria in the study.
You may qualify if:
- The person must be 18 years of age or older,
- Must volunteer to participate in the research.
You may not qualify if:
- The person must be 18 years of age or younger,
- Not willing to participate in the study,
- The person must be in ASA VI class,
- Death must have been considered during surgery.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Zonguldak Atatürk State Hospital
Zonguldak, Zonguldak Province, 67100, Turkey (Türkiye)
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- CROSS SECTIONAL
- Target Duration
- 3 Months
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Principal Investigator
Study Record Dates
First Submitted
January 12, 2026
First Posted
February 3, 2026
Study Start
April 1, 2025
Primary Completion
July 1, 2025
Study Completion
July 1, 2025
Last Updated
February 3, 2026
Record last verified: 2026-01
Data Sharing
- IPD Sharing
- Will not share
Patients' personal information was not included in the study and will not be shared.