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First Attempt Insertion Success of Novel Two Person Lateral Rotation Technique V.S Standard Brain Technique for LMA Insertion

NCT07715708 · tracked via the Priya Life Science Egypt tracker
Phase
Not applicable
Started
2026-07-01
Last updated
2026-07-20

Condition(s) studied

LMAVentilation

Investigational drug(s) / intervention(s)

LMA insertion by Standard techniqueLMA insertion by Two-Person Lateral Rotation Technique

LMA insertion by Standard technique: Standard Brain Technique for Laryngeal Mask Airway Placement

LMA insertion by Two-Person Lateral Rotation Technique: Novel Two-Person Lateral Rotation Technique of LMA insertion

Study summary

The goal of this clinical trial is to learn if two person lateral rotation technique of LMA insertion is more successful than the standard technique in achieving effective ventilation on the first introduction of the LMA .The main questions it aims to answer are:

Does two person lateral rotation technique of LMA insertion lower the number of times needed to inesrt the LMA ?

Researchers will compare two person lateral rotation technique of LMA insertion to standard technique to see if it is more successful

Participants will be subjected to the two way of LMA insertion

Eligibility

Sex
ALL
Min age
18 Years
Max age
65 Years
Healthy volunteers
No
Inclusion Criteria: * Adult patients aged 18-65 years * American Society of Anesthesiologists (ASA) physical status I-II * Scheduled for elective superficial surgical procedures under general anesthesia (e.g., limb orthopedic surgery, hernioplasty, soft tissue excision) * Anticipated surgical duration \< 90 minutes * Body mass index (BMI) 18.5-30 kg/m² Exclusion Criteria: * \- Anticipated difficult airway (Mallampati grade IV, thyromental distance \< 6 cm, limited neck extension) * History of gastroesophageal reflux disease or increased aspiration risk * Full stomach or emergency surgery - Intra-abdominal, laparoscopic, head and neck, or prone-position procedures - Known allergy to anesthetic agents * Pregnancy * Previous pharyngeal or laryngeal surgery - Inability to provide informed consent

Primary outcome measure(s)

  • First-attempt insertion success rate, defined as successful placement achieving effective ventilation on the first introduction of the LMA into the oral cavity — 1 minute after LMA insertion

Trial sites (1)

FacilityCityRegionStatus
Benha University Hospital Banhā Egypt

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07715708 on ClinicalTrials.gov ↗ ← All trials in Egypt