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NOT YET RECRUITING
NCT01003028
PHASE4

Reduction of Remifentanil-related Complications

Sponsor: Seoul National University Hospital

View on ClinicalTrials.gov

Summary

This study is intended to evaluate the effect of decreasing the maximum plasma concentration target of remifentanil of the Target Controlled Infusion system on the the incidence of major and minor side-effects.

Official title: Reduction of Remifentanil-related Complications by Limiting Maximum Plasma Concentration During Target-controlled Infusion

Key Details

Gender

All

Age Range

18 Years - 70 Years

Study Type

INTERVENTIONAL

Enrollment

160

Start Date

2024-11-01

Completion Date

2026-12-01

Last Updated

2023-12-01

Healthy Volunteers

No

Conditions

Interventions

DRUG

Remifentanil (Limited) - Target Controlled Infusion system

Limit max plasma concentration to 9.8 ng/ml

DRUG

Remifentanil (Control) - Target Controlled Infusion system

Use 20 ng/ml as max plasma concentration

Locations (1)

Seoul National University Hospital

Seoul, South Korea