- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06925165
Ultrasound Measured Hyomental Distance to Tongue Thickness Ratio as a Predictor of Difficult Intubation in Infants
Study Overview
Status
Conditions
Detailed Description
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
-
-
-
Cairo, Egypt, 11111
- Ain Shams University
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- Infants aged 1 to 12 months
Both sexes.
Physical status ASA I or II
Exclusion Criteria:
- Restricted mobility of temporomandibular joint
- Absent anesthesia or surgical consent
- Maxillofacial trauma or tumors
- A large mass or scar under the chin
Study Plan
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
role of ultrasound measured hyomental distance to tongue thickness ratio in predicting difficult intubation in infants.
Time Frame: 2 to 3 minutes after induction of anaesthesia and intubation
|
Difficult intubation can be a significant life threatening problem in anesthesia which can lead to serious complications like hypoxia, aspiration, esophageal intubation, emergency surgical airway, cardiovascular instability, cardiac arrhythmias, ischemic encephalopathy, and death. In the study investigators will use hyomental distance and tongue thickness measured by ultrasound to suspect difficult intubation in infants aged 1 to 12 month. |
2 to 3 minutes after induction of anaesthesia and intubation
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Shaimaa Reda Ahmed, MBBCH, Anesthesia resident Ain Shams University
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
- FMASU MS 53/2025
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
IPD Sharing Time Frame
IPD Sharing Access Criteria
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
product manufactured in and exported from the U.S.
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.
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