Comparison of Nasogastric Tube Insertion Success in Difficult and Easy Airway Patients
1 other identifier
observational
244
1 country
1
Brief Summary
This research aims to investigate potential variations in the success rate and occurrence of complications during nasogastric tube insertion between Difficult and Easy Airway Patients.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Aug 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
First Submitted
Initial submission to the registry
August 16, 2023
CompletedFirst Posted
Study publicly available on registry
August 21, 2023
CompletedStudy Start
First participant enrolled
August 28, 2023
CompletedPrimary Completion
Last participant's last visit for primary outcome
February 28, 2024
CompletedStudy Completion
Last participant's last visit for all outcomes
March 28, 2024
CompletedMay 2, 2024
April 1, 2024
6 months
August 16, 2023
April 30, 2024
Conditions
Outcome Measures
Primary Outcomes (1)
Comparison of Nasogastric Tube Insertion in Difficult and Easy Airway Patients
The main aim was to investigate whether there is a difference between the groups in terms of the success of insertion of the nasogastric tube (first attempt, second attempt etc.) and the duration of insertion
10 minutes
Secondary Outcomes (2)
Complications in Difficult and Easy Airway Patients
5 minutes
Airway parameters and failure of nasogastric tube insertion
10 minutes
Eligibility Criteria
Patients who are scheduled for surgery for any reason and who will receive general anesthesia requiring perioperative nasogastric tube insertion will be included in the study.
You may not qualify if:
- Patients under 18 year-old
- Patients who do not require nasogastric tube insertion
- Patients with anatomical changes in the head and neck region
- Patients without an informed consent form
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Taksim Training and Research Hospital
Istanbul, Please Select, 34433, Turkey (Türkiye)
Study Officials
- PRINCIPAL INVESTIGATOR
Celal Kaya, MD
Taksim Training and Research Hospital
Study Design
- Study Type
- observational
- Observational Model
- CASE ONLY
- Time Perspective
- CROSS SECTIONAL
- Target Duration
- 1 Day
- Sponsor Type
- OTHER GOV
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
August 16, 2023
First Posted
August 21, 2023
Study Start
August 28, 2023
Primary Completion
February 28, 2024
Study Completion
March 28, 2024
Last Updated
May 2, 2024
Record last verified: 2024-04