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COMPLETED
NCT01893723
NA

Analgesia Nociception Index Guided Remifentanil Administration During Propofol Anesthesia for Laparoscopic Surgery

Sponsor: University Hospital, Lille

View on ClinicalTrials.gov

Summary

The Physiodoloris (MetroDoloris, Lille, France) monitor, CE marqued, uses the ECG signal in order to compute the Analgesia Nociception Index (ANI) which has been shown to measure the relative parasympathetic tone, and hence to reflect the analgesia/nociception balance during general anesthesia. The primary endpoint of this randomized multicenter study is to measure whether there is a benefit to use the ANI in order to adapt remifentanil administration during propofol anesthesia for laparoscopic surgery. Primary endpoint : lesser proportion of patients presenting with at least one episode of hemodynamic reactivity, hypotension or bradycardia in the ANI guided group vs control group ?

Official title: Analgesia Nociception Index Guided Remifentanil Administration During Propofol Anesthesia for Laparoscopic Surgery : Multicenter Randomized Clinical Trial

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

INTERVENTIONAL

Enrollment

37

Start Date

2012-06

Completion Date

2015-05

Last Updated

2026-04-21

Healthy Volunteers

No

Interventions

PROCEDURE

ANI guided remifentanil

remifentanil administration during propofol anesthesia for laparoscopic surgery is ANI guided

PROCEDURE

ANI blind arm

remifentanil administration during propofol anesthesia for laparoscopic surgery is not ANI guided

Locations (5)

University Hospital Erasme (ULB)

Brussels, Belgium

Clinique privée d'ANTONY

Antony, France

University Hospital Claude Huriez

Lille, France

University Hospital Roger Salengro

Lille, France

University Hospital

Saint-Etienne, France