drugset / Trial / NCT06237101

Remifentanil Effect on Burst Suppression Ratio

NCT06237101

Recruiting 20 enrolled University of Chile
RandomizedCrossoverSingle-blindBasic science

Summary

The goal of this clinical trial is to determine whether remifentanil has a facilitating effect on the generation of burst suppression by propofol in adult patients (18-60 years) candidates for elective surgery who require remifentanil and American Society of Anesthesiology (ASA) classification I or II. The main question it aims to answer are: • To determine whether remifentanil has a facilitating effect on the generation of burst suppression by propofol. Participants will undergo general anesthesia with remifentanil and propofol sequentially. After loss of consciousness, remifentanil will be adjusted to a medium or high concentration randomly and it will be determined at what concentration of propofol the burst suppressions are generated. Then, the concentrations of propofol that generate burst suppression associated with either a medium or high concentration of remifentanil will be compared.

Timeline

Start
2024-03-01
Primary completion
2026-08-31
Completion
2026-09-30

Drugs

EvaluationDrugModalityDoseRoute
Subject Remifentanil Small molecule 4 ng/ml
Subject Remifentanil Small molecule 7.5 ng/ml

Indications

No indication recorded.