ProVu Video Stylet With Versus Without the Fekry Airway

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

Status

Recruiting

Phases

Unknown

Study type

Interventional

Source

ClinicalTrials.gov

Registry ID

NCT07568743

Enrollment

130

Registered

2026-05-06

Start date

2026-05-10

Completion date

2026-10-10

Last updated

2026-05-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Endotracheal Intubation, Video Rigid Stylet

Brief summary

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

DEVICEProVu video stylet

Group C (n=55): Intubation using the ProVu video stylet without the Fekry Airway.

DEVICEProVu video stylet and Fekry Airway

Group F (n =55): endotracheal Intubation assisted by the ProVu video stylet and using Fekry Airway

Study design

Allocation

RANDOMIZED

Intervention model

PARALLEL

Primary purpose

HEALTH_SERVICES_RESEARCH

Masking

DOUBLE (Subject, Investigator)

Eligibility

Sex/Gender

ALL

Age

18 Years to 65 Years

Healthy volunteers

Yes

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.

Design outcomes

Primary

Measure	Time frame	Description
Time to successful intubation	within 15 minutes preoperatively	It is defined as time in seconds elapsing from touching assimply of ProVu video stylet to insisors (C group)or to Fekry Airway ( F group) till connecting the endotracheal tube to ventlatory circuate after removal of assimply

Countries

Egypt

Contacts

CONTACTReham Ali Abdelrahman, Assistant Professor, M.D.

rehamali72@hotmail.com01009136408

CONTACTReham Ali Abdelhaleem Abdelrahman, M.D. 00201009136408, M.D.

rehamali72@hotmail.com

PRINCIPAL_INVESTIGATORReham Ali Abdelrahman

Cairo University

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: May 9, 2026