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Which intubation method keeps heart rate and blood pressure more stable?

NCT ID NCT06487988

Knowledge-focused Sponsor: American University of Beirut Medical Center Source: ClinicalTrials.gov ↗

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed This study
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 27, 2026 · Last updated Aug 11, 2026 · Updated 2 times

Summary

This study compares two methods of placing a breathing tube during general anesthesia without using opioid painkillers. The goal is to see which method—fiberoptic or direct laryngoscopy—causes less change in heart rate and blood pressure. Researchers will study 90 adults aged 18 to 55 having elective surgery. They will also check how long intubation takes and if patients have sore throat, hoarseness, or airway injury afterward.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

What this could lead to
If fiberoptic intubation proves more stable, it could guide safer anesthesia practices for patients who cannot receive opioids.
What could go wrong
This is a small, early-stage study (90 participants) focused on short-term vital signs, not long-term outcomes. Results may not apply to all patients or settings.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Phase

Not a phased trial

Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.

Participants

68 people

The number who actually took part.

Started

Sep 2024

Finished

Jun 2026

Lead sponsor

Other sponsor

The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Ages

18 to 55 years

Sex

Anyone

Healthy volunteers

Accepted

You do not need to have the condition being studied to take part.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: * ASA (American Society of Anesthesiologists) physical status I and II * Range age of 18-55 years' old * Scheduled for elective surgery under general anesthesia. Exclusion Criteria: * History of cardiovascular diseases. * History of lung disease. * Hypertensive patient (BP\> 140/90) * Patient taking medications that affect blood pressure and heart rate * Morbid obesity (BMI \>30) * Severe GERD * Predicted difficult airway (Short TMD \<6 cm, Upper li bite test grade III, Mallampati score \>III) * Neck instability * Patient planned to receive rapid sequence intubation * Patient refusal to participate * History of difficult intubation/ ventilation

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Conditions

The condition(s) this trial relates to.

hypertensive disorder

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Analgesics, opioid Anesthesia, general Blood pressure Heart rate

Contacts and locations

Locations

  • Christian Rouphael

    Beirut, Lebanon

More trials for these conditions

Other studies related to the condition(s) this trial covers.