- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07841392
Recall and Perceived Applicability of Ganzouri Airway Scoring System Versus LEMON Score for Airway Assessment Among Anesthesia Residents
Comparison of Recall and Perceived Applicability of Ganzouri Airway Scoring System Versus LEMON Score for Airway Assessment Among Anesthesia Residents; a Prospective Observational Study
Our aim is to compare the recall and perceived clinical applicability of Ganzouri airway scoring system versus LEMON score for airway assessment from residents' perspective.
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Securing a patent airway stands as one of the most fundamental obligations in anesthetic practice, and the timely recognition of a potentially difficult airway prior to induction is of paramount importance for patient safety.
Two of the most widely recognized examples are the Ganzouri Airway Scoring system and the LEMON score. The Ganzouri Airway scoring system integrates seven distinct clinical parameters; mouth opening, thyromental distance, Mallampati classification, neck range of motion, ability to prognath, body weight, and history of prior difficult intubation, each carrying a weighted numerical value whose sum reflects the probability of encountering a difficult airway.
Study Type
Enrollment (Estimated)
Contacts and Locations
Study Contact
- Name: Ghada A Sherif, MD
- Phone Number: 00201006153615
- Email: drghadasherif@gmail.com
Study Locations
-
-
-
Cairo, Egypt, 12613
- Recruiting
- Cairo University
-
Contact:
- Ghada A Sherif, MD
- Phone Number: 00201006153615
- Email: drghadasherif@gmail.com
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
This study was designed as a prospective observational educational study that compared the recall and perceived clinical applicability of two airway assessment scoring systems: the Ganzouri Airway Score and the LEMON Score
Description
Inclusion Criteria:
- Enrolled anesthesiology residents.
- Currently training at Kasr Al-Ainy Hospitals.
- Willing to participate and provide informed consent.
- Available for entire study duration (baseline through 2-week followup).
- First-year residents who didn't receive training in Ganzouri or LEMON Airway scoring systems.
Exclusion Criteria:
- Residents with prior formal training in either Ganzouri or LEMON Airway scoring systems (defined as structured lecture or workshop exceeding 30 minutes).
- Residents who will be on leave, rotation at external sites, or otherwise unavailable during the 2-week follow-up period.
- Refusal to participate or provide consent.
Study Plan
How is the study designed?
Design Details
- Observational Models: COHORT
- Time Perspectives: PROSPECTIVE
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
Study group
First-year residents who didn't receive training in Ganzouri or LEMON Airway scoring systems. |
This scoring system evaluates seven parameters:
The LEMON mnemonic represents:
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Mean total immediate recall score
Time Frame: Within 30 minutes after completion of the educational lectures
|
The total immediate recall score was assessed using a structured recall checklist within 30 minutes after completion of the educational lectures. |
Within 30 minutes after completion of the educational lectures
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Mean total delayed recall score at Day 14
Time Frame: 14 days after completion of the educational lectures
|
The total delayed recall score will be assessed using the same structured recall checklist 14 days after completion of the educational lectures. |
14 days after completion of the educational lectures
|
|
Resident satisfaction
Time Frame: 14 days after completion of the educational lectures
|
Residents' satisfaction was assessed using a structured post-lecture questionnaire with five-point Likert-scale responses. |
14 days after completion of the educational lectures
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- MS-225-2026 (1-7-2026)
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
The data will be available upon a reasonable request from the corresponding author after the end of study for one year.
IPD Sharing Time Frame
After the end of study for one year.
IPD Sharing Access Criteria
The data will be available upon a reasonable request from the corresponding author.
IPD Sharing Supporting Information Type
- STUDY_PROTOCOL
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.