Skip to main content
OpenTrials
Completed

NCT Number: NCT07382895

The Relationship Between the ASA Score Determined by Operating Room Nurses and Intubation Duration

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.

Completed

Looking for future studies?

Notify Me

Key information

Age range

18 year–100 year

Sex eligibility

All sexes

Study type

Observational

Primary location

Zonguldak Atatürk State Hospital

Zonguldak, Zonguldak Province, 67100, Turkey (Türkiye)

About this study

The present research is to be conducted as a prospective observational study. The present prospective observational study is to be conducted over a 3-month period between April 1, 2025, and July 1, 2025, at a single centre, with the involvement of 36 nurses, 12 anesthesiologists (12 operating tables), and 80 patients working in the operating room of Zonguldak Atatürk State Hospital, who evaluate patients in a pre- and post-operative assessment clinic. The sociodemographic information of the nurses and anesthesiologists will be recorded using "Personal Information Form 1" and "Personal Information Form 2". Prior to undergoing surgery, patients' ASA scores and sociodemographic information will be evaluated by operating room nurses and anesthesiologists, who will record this data using "Personal Information Form 3". Patients will be followed up until they are discharged from the clinic, and their mechanical ventilation needs will be recorded. The ASA scores assigned by operating room nurses and anesthesiologists will be analysed in relation to the necessity for mechanical ventilation.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • The person must be 18 years of age or older,
  • Must volunteer to participate in the research.

Exclusion criteria

  • 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.

Treatment and study plan

Primary outcomes

  1. Determining the sociodemographic information of the nurse using "Personal Information Form 1"

    Time frame: From April 2025 to June 2025

    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.

  2. Determining the sociodemographic information of anesthesiologists using "Personal Information Form 3"

    Time frame: From April 2025 to June 2025

    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.

  3. Determining the sociodemographic information of the patient's using "Personal Information Form 3"

    Time frame: From April 2025 to June 2025

    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.

Secondary outcomes

  1. Comparing patients' ASA scores with their need for mechanical ventilation

    Time frame: From April 2025 to June 2025

    The ASA scores given to patients by operating room nurses and anesthesiologists will be compared with the likelihood of them needing mechanical ventilation. For analyzing the differences between two independent groups with a normal distribution, an independent t-test will be applied; for analyzing the differences between more than two independent groups, an ANOVA test will be applied.

Sponsors and collaborators

Lead sponsor

Zonguldak Bulent Ecevit University

Other

Collaborators

  • Zonguldak Ataturk State Hospital

Registry information

Important dates

Study start
2025
Primary completion
2025
Study completion
2025
First posted
Feb 3, 2026
Registry last updated
Feb 3, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.