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NOT YET RECRUITING
NCT06684197
NA

The Impact of a Dexmedetomidine Perfusion on Intraoperative Remifentanil Consumption

Sponsor: Ciusss de L'Est de l'Île de Montréal

View on ClinicalTrials.gov

Summary

Opioids analgesic are the gold standard for intraoperative pain management. Their short- and long-term adverse effect motivate anesthesiologists to explore opioid sparing strategies. Dexmedetomidine is a highly selective α2 adrenergic receptor agonist that could help minimize opioid consumption both intraoperative and postoperative due to its sedative, analgesic and sympatholytic properties. This new randomized controlled trial (RCT) will answer the question whether an intraoperative dexmedetomidine infusion compared to placebo has a clinically significant impact on intraoperative remifentanil consumption during a laparoscopic abdominal elective surgery.

Official title: The Impact of a Dexmedetomidine Perfusion on Intraoperative Remifentanil Consumption: a Randomized Controlled Trial

Key Details

Gender

All

Age Range

18 Years - 80 Years

Study Type

INTERVENTIONAL

Enrollment

72

Start Date

2024-11

Completion Date

2025-11

Last Updated

2024-11-12

Healthy Volunteers

Yes

Interventions

DRUG

Dexmedetomidine

Intravenous dexmedetomidine will be given as a bolus (0.5 μg.kg-1) over 10 minutes. A perfusion of 0.5 mcg.kg-1.h-1 of dexmedetomidine will be programmed and maintained up until the pneumoperitoneum is deflated or up until a total dose of 2.5μg.kg-1 has been administered.

DRUG

Placebo

Saline will be used instead of dexmedetomidine

Locations (1)

Hôpital Maisonneuve-Rosemont

Montreal, Quebec, Canada