Status:
TERMINATED
Analgesia Nociception Index Guided Remifentanil Administration During Propofol Anesthesia for Laparoscopic Surgery
Lead Sponsor:
University Hospital, Lille
Conditions:
General Anesthesia
Eligibility:
All Genders
18+ years
Phase:
NA
Brief 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 parasymp...
Detailed Description
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 parasymp...
Eligibility Criteria
Inclusion
- laparoscopic cholecystectomy or gynecological laparoscopic surgery
- ASA I or II
- adult patient
- body mass index between 17 and 33 kg/m2
Exclusion
- pregnancy
- arrhythmia
- pace maker
- diabetes mellitus
- dysautonomia
- treatment with beta blocking agents
Key Trial Info
Start Date :
June 1 2012
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
May 1 2015
Estimated Enrollment :
37 Patients enrolled
Trial Details
Trial ID
NCT01893723
Start Date
June 1 2012
End Date
May 1 2015
Last Update
November 4 2015
Active Locations (5)
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1
University Hospital Erasme (ULB)
Brussels, Belgium, 1070
2
Clinique privée d'ANTONY
Antony, France, 92160
3
University Hospital Claude Huriez
Lille, France, 59000
4
University Hospital Roger Salengro
Lille, France, 59000