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Comparison of Post-intubation Hyperdynamic Responses Following Induction with Propofol 2 mg/kg versus Split-dose Propofol (1.5 mg/kg + 0.5 mg/kg) with Fentanyl: A Double-blind Randomized Controlled Trial

Comparison of Post-intubation Hyperdynamic Responses Following Induction with Propofol 2 mg/kg versus Split-dose Propofol (1.5 mg/kg + 0.5 mg/kg) with Fentanyl: A Double-blind Randomized Controlled Trial

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
TCTR
Registry ID
TCTR20260708007
Enrollment
100
Registered
2026-07-08
Start date
2026-08-03
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

Post-intubation hyperdynamic alteration after propofol induction and post-induction hypotension. Propofol, post-intubation hypertension, post-induction hypotension.

Interventions

Aneshtesia induction with propofol 2 mg/kg IV,propofol 1.5 mg/kg IV for induction with propofol 0.5 mg/kg 30 seconds before tracheal intubation
Active Comparator Other,Active Comparator Other
The control group,The split-dose group

Sponsors

None listed

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Aged 18-65 years. 2. American Society of Anesthesiologists (ASA) physical status classification I or II. 3. Undergoing elective non-cardiac surgery under general anesthesia with endotracheal tube.

Exclusion criteria

Exclusion criteria: 1. History of hypersensitivity to propofol, soy bean and egg lecithin. 2. Hypertensive participants who consumed angiotensin converting enzyme (ACE) inhibitor or angiotensin receptor blocker (ARB). 3. Blood pressure before the induction of anesthesia more than 160/100 mmHg or less than 90/60mmHg, heart rate less than 60 bpm or more than 120 bpm 4. Anticipated difficult airway. 5. At risk of full stomach. 6. Body mass index more than or equal 30 kg/m2. 7. History of Arrhythmia e.g. premature ventricular contraction, atrial fibrillation, atrial flutter, mobitz type I, mobitz type II, third degree AV block, ventricular tachycardia, wolff-parkinson-white syndrome, supraventricular tachycardia. 8. Participants who required propofol titration during induction, or those unable to receive the dose as specified in the protocol. 9. Unsuccessful intubation at the first time.

Design outcomes

Primary

MeasureTime frame
post-intubation hyperdynamic response immediate post-intubation mean arterial pressure in units of millimeters of mercury (mmHg)

Secondary

MeasureTime frame
other hemodynamic parameter from induction to 5 minutes after intubation systolic blood pressure, diastolic blood pressure, mean arterial pressure and heart rate in units of millimeters of mercury (mmHg),the change in mean arterial pressure from baseline to immediate post-intubation, and from pre-intubation to immediate post-intubation mean arterial pressure in units of millimeters of mercury (mmHg),incidence of post induction hypotension from induction to 5 minutes after intubation mean arterial pressure in units of millimeters of mercury (mmHg)

Countries

Thailand

Contacts

Public ContactPariya Plicharoenpon

Chaoprayaymmarat hospital

p.pariya@gmail.com0818802218

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 10, 2026