Ultrasonographical Assessment of Airway Indices in Pregnancy
Clinical and Ultrasonographic Assessment of Airway Indices Among Nonpregnant, Normotensive Pregnant and Pre-eclamptic Patients: a Prospective Observational Study
1 other identifier
observational
180
1 country
1
Brief Summary
Clinical and ultrasound indices of airway, in addition to laryngoscopic view will be assessed and compared among three groups of patients: non pregnant, pregnant with normal blood pressure, preeclampsia patients undergoing various surgeries under general anesthesia.
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 Dec 2024
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
December 15, 2024
CompletedFirst Submitted
Initial submission to the registry
November 25, 2025
CompletedFirst Posted
Study publicly available on registry
February 20, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
November 1, 2026
ExpectedStudy Completion
Last participant's last visit for all outcomes
December 1, 2026
February 20, 2026
February 1, 2026
1.9 years
November 25, 2025
February 17, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Sperficial ultrasonographic airway assessemt
By using superficial ultrasound probe, we measure in millimeters: anterior neck skin to hyoid bone distance, anterior neck skin to vocal cord distance (ANS-VC) ,distance from the epiglottis to the midpoint of the distance between the vocal cords (E-VC),the depth of pre-epiglottic space (Pre-E) and Pre-E/E-VC ratio). All parameters will be measured in millimeters in all groups by the same doctor, and the same ultrasound device.
preoperative just before induction of anesthesia
Secondary Outcomes (3)
Assessment of laryngoscopic view
preoperative just before endotracheal intubation
Tongue thickness
Once just before induction of general anesthesia
Hyoid bone visibility
Preoperative just before induction of anesthesia
Study Arms (3)
Non Pregnant
non pregnant patients undergoing surgery under general anesthesia
pregnant normotensive
pregnant normotensive patients undergoing surgery under general anesthesia
preeclampsia
preeclampsia patients undergoing surgery under general anesthesia
Eligibility Criteria
non pregnant, normotensive pregnant and preeclamptic patients who are undergoing general anesthesia, and also apply to the inclusion criteria and have non of the exclusion criteria mentioned above.
You may qualify if:
- normotensive pregnant
- pre-eclamptic patients.
- nonpregnant females in child bearing period .
You may not qualify if:
- Patients excluded were women at \<32 weeks' gestation or with Eclampsia .
- height \<150 cm, body mass index (BMI) \>30 kg/m2 .
- predicted airwy difficulty due to any other cause as neck swelling , facial deformity and prominent teeth.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Qena University
Qina, Qena Governorate, 83511, Egypt
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Central Study Contacts
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- CROSS SECTIONAL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- lecturer in anesthesia, Intensive Care and Pain Management
Study Record Dates
First Submitted
November 25, 2025
First Posted
February 20, 2026
Study Start
December 15, 2024
Primary Completion (Estimated)
November 1, 2026
Study Completion (Estimated)
December 1, 2026
Last Updated
February 20, 2026
Record last verified: 2026-02
Data Sharing
- IPD Sharing
- Will not share