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Recruiting NCT07568743

ProVu Video Stylet With Versus Without the Fekry Airway

No phase Interventional Endotracheal Intubation Video Rigid Stylet

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: ProVu video stylet, ProVu video stylet and Fekry Airway.
Who it may be relevant to
Registry conditions: Endotracheal Intubation, Video Rigid Stylet. Basic parameters: 18 years — 65 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Egypt
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

Comparison of Intubation Time and Performance Between the ProVu Video Stylet With Versus Without the Fekry Airway in Adults With Normal Airway: A Single-Blinded Randomized Controlled Trial

Overview

This study aimed to compare assisted intubation using the ProVu video stylet device passing through Fekry airway versus intubation without the use of Fekry airway . The investigators hypothesized that endotracheal intubation assisted by ProVu video stylet using the Fekry airway as a conduit for intubation would improve the glottic visualization and the higher first attempt success rate when compared to endotracheal intubation assisted by ProVu video stylet without using the Fekry airway.

Interventions

  • Device ProVu video stylet
    Group C (n=55): Intubation using the ProVu video stylet without the Fekry Airway.
  • Device ProVu video stylet and Fekry Airway
    Group F (n =55): endotracheal Intubation assisted by the ProVu video stylet and using Fekry Airway

Primary outcome measures

  • Time to successful intubation [Time frame: within 15 minutes preoperatively]

Eligibility criteria

Inclusion criteria

  • • American Society of Anesthesiologists (ASA) physical status I, II.
  • Patients scheduled for elective surgery requiring general anesthesia and orotracheal intubation of less than 2 hours duration .
  • Ganzouri Airway score <3.

Exclusion criteria

  • Patient with Active cardiac condition.
  • Patient with airway congenital anomaly.
  • Mallampati score III or IV.
  • Body mass index (BMI) > 35 kg/m² (obesity).
  • Limited cervical spine mobility.
  • History of difficult intubation, upper airway surgery, or trauma.
  • Facial or oropharyngeal deformities.
  • Allergy or contraindication to study medications.
  • Refusal to participate.

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Double blind
Primary purpose
Health services research

Study locations

Egypt · 2 centers
  • Faculty of Medicine-Cairo University — Cairo
  • Reham Ali Abdelhaleem Abdelrahman — Cairo

Identifiers

NCT: NCT07568743 · IDDS-2026

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗