New study tests safer dosing of Heart-Stabilizing drug during breathing tube insertion
NCT ID NCT06327399
First seen Jun 25, 2026 · Last updated Jul 10, 2026 · Updated 3 times
Summary
This study tested two methods of giving the drug dexmedetomidine to 70 adults during intubation (placing a breathing tube). One group received a slow infusion over 10 minutes, the other a quick bolus over 60 seconds. The goal was to see which method causes fewer changes in heart rate and blood pressure. Researchers also tracked any episodes of very slow heart rate or low blood pressure that needed rescue medication.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Dexmedetomidine
- What this could lead to
- If it works, this could point toward a safer way to give dexmedetomidine during intubation, reducing heart rate and blood pressure swings.
- What could go wrong
- This is a small, completed Phase 2 trial with only 70 participants. Results may not apply to all patients, and the drug can still cause slow heart rate or low blood pressure.
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
-
Phase 2
Tests whether the treatment actually works, and watches for side effects, in a larger group.
- Participants
-
70 people
The number who actually took part.
- Started
-
Apr 2024
- Finished
-
Sep 2024
- 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 50 years
- Sex
-
Anyone
- Healthy volunteers
-
Accepted
You do not need to have the condition being studied to take part.
Show the full entry requirements Hide 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 I and II patients. * Mallampati grade I and II. Exclusion Criteria: * Patient refusal. * Morbid obesity. * Predicted difficult airway/unanticipated difficult intubation or laryngoscopic attempt lasting greater than 15 seconds or two attempts or more. * Patients with uncontrolled sepsis. * Pregnancy or breast feeding. * Patients with renal impairment i.e. SCr ≥ 1.5 * Any patient on regular intake of beta blockers or calcium channel blockers. * CNS disorders.
Get updates
Get notified about this study
Sign up to get updates when this study changes or when new studies for Dexmedetomidine are added.
Genom att skicka in godkänner du våra Användarvillkor
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
-
Cairo University Hospitals
Giza, Giza Governorate, 11562, Egypt
More trials for these conditions
Other studies related to the condition(s) this trial covers.
- Can a sedative plus ear stimulation stop PTSD before it starts?
- Can a Mini-Dose drug combo rescue Post-Surgery sleep for sleep apnea patients?
- Can a nasal spray calm nerves before brain surgery?
- Could a common sedative shield aging brains from Post-Surgery delirium?
- Could a Two-Drug anesthesia combo lift Post-Surgery mood?
- Can a simple infusion make sinus surgery safer and clearer?