CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 34 enrolled
Drug / intervention
BISdevice
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT04466384
NCT04466384N/ACompleted
CompareCT.gov

Bispectral Index and Levels of Sedation With Propofol With/Without Remifentanil in Healthy Volunteers (SONORA)

Medtronic - MITG·interventional·Posted Jul 10, 2020·Updated Jul 19, 2022

In Brief

A clinical study evaluating BIS for Anesthesia. Completed, enrolled 34 participants across 1 site.

Detailed Summary

The purpose of this study is investigate the relationship between BIS™ and propofol with/without remifentanil across a wide range of hypnotic states.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsAnesthesia
CountriesUnited States
Collaborators--

Timeline

N/ACompletedFinished
202120222023202420252026
First PostedJul 10, 2020
Enrollment StartAug 11, 2020
Primary CompletionMar 3, 2021
TodayJul 2, 2026
Enrollment to primary: 7 monthsPosted 6.0 years ago

Interventions

BISdevice

Subjects will be sequentially assigned to the propofol or propofol and remifentanil group. The purpose is to capture the BIS value in association with these anesthetics.