CClinicalTrials.gg
Not yet recruitingNCT06924411Updated Apr 11, 2025

Ramped Versus Supine Position for Emergent Endotracheal Intubation in Adult Patients; Prospective, Randomized, Comparative Study

An interventional study of Direct Intubation in Intubation Complications, sponsored by Sohag University. Not yet recruiting. Open to participants aged 14 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2025-04-11.

Sponsored by Sohag University · Not applicable, Interventional, and Prevention

From the registry’s dates

  • Primary completion was expected by Jul 2025, 1 year 3 months ago, but the record still lists the study as not yet recruiting.
Phase
Not applicable
Study type
Interventional
Enrollment
100
Allocation
Randomized
Ages
14 Years and older
Sex
All
01

Study summary

Endotracheal intubation is a life saving procedure for critically unwell and injured patients presenting to the emergency department. Prolonged time to successful intubation and multiple failed attempts are associated with a higher incidence of life-threatening adverse events such as hypoxia and hypotension.

Optimal head and neck positioning and clinical experience are important factors for successful endotracheal intubation in patients especially with a difficult airway. This study aims to investigate the rate of successful endotracheal intubation between ramped and supine positions in patients planned for intubation.

The ramped position, where the bed is kept half-flat and the head is elevated up to 35°, is planned to prove that it improves glottic view and facilitate intubation and ventilation.

Varying bed angles and heights during ramped position intubation may explain conflicting evidence regarding the effect of ramped position on intubation success in acute care settings.

Therefore, it seems that finding a simple alternative method for the classic supine technique that can create conditions like the proposed standard conditions for laryngoscopy would be a suitable solution for intubating patients with higher difficulty.

The patient's anatomy and the technique employed for laryngoscopy have a significant effect on the laryngeal view. The technique itself is influenced by a variety of factors including the laryngoscopic force and the skills, experience, and training of the physicians.

02

Conditions studied

  • Intubation Complications

Keywords

  • Ramped intubation
  • Non-supine intubation
  • Semi-setting intubation
  • Intubation without aspiration
  • Ramped versus supine intubation
  • Intubation with less complications
03

In context

Lead sponsor

Sohag University is the lead sponsor of 1,183 studies on the registry; 612 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
14 Years and older
Sexes eligible
All
Accepts healthy volunteers
Yes

Inclusion criteria

  • Adult patients ≥18 years old and indicated for intubation with variable presentations.

Exclusion criteria

Exclusion Criteria:

  • Patients unstable to be positioned in semi setting as spine trauma and polytraumatized patients.
05

Study design

Phase
Not applicable
Primary purpose
Prevention
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
100 participants (estimated)

Study arms

  • Active comparator
    Supine group

    Intubation in supine position

    Device: Direct Intubation

  • Active comparator
    Ramped group

    Intubation in ramped position

    Device: Direct Intubation

Interventions

  • DeviceDirect Intubation

    Direct laryngoscopy intubation

06

What researchers measure

Primary outcomes

  1. Number of First pass success

    Successful intubation from first trial

    Time frame: 6 months

07

Study locations

No study locations are listed for this record.

08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Apr 11, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT06924411
Lead sponsor
Sohag University
Responsible party
Mohamed Aly Hashem (Resident doctor, Sohag University) — Principal investigator
First posted
Apr 11, 2025
Start date
May 2025 (estimated)
Primary completion
Jul 2025 (estimated)
Completion
Sep 2025 (estimated)
Last update
Apr 11, 2025

Study contacts

Mohamed A Hashem
Contact
Mohamed.hashem@med.sohag.edu.eg
+201100074625 ext. Resident
Fawzy A Badawy
Contact

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is not yet recruiting, as verified in Apr 2025. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion