Status:
COMPLETED
Factors Influencing Anesthetic Drug Requirement
Lead Sponsor:
Hopital Foch
Conditions:
Anesthesia, General
Eligibility:
All Genders
18+ years
Phase:
NA
Brief Summary
The main objective of the study is to analyze the influence of several environmental (i.e., timing: seasonal, circadian) and demographic conditions (i.e., age, gender, menstrual cycle) on anesthetic d...
Eligibility Criteria
Inclusion
- Patients undergoing scheduled surgery under general anesthesia, agreeing to participate in the study
Exclusion
- Age under 18 years
- Pregnancy, breastfeeding woman
- Allergy to propofol, soybeans or peanuts
- Allergy to sufentanil, remifentanil, morphine,
- Allergy to a muscle relaxant or to any of its excipients
- Known hypersensitivity to sufentanil, remifentanil, or to other derivates of fentanyl
- History of central neurological disorder or brain injury
- Patient with dementia
- Patient with pacemaker
- Patient receiving psychotropic drugs or morphine agonist-antagonists
- Surgery on the skull and/or operating position preventing the use of a bispectral index sensor in suitable conditions
Key Trial Info
Start Date :
May 4 2009
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
July 31 2017
Estimated Enrollment :
3278 Patients enrolled
Trial Details
Trial ID
NCT00896714
Start Date
May 4 2009
End Date
July 31 2017
Last Update
August 14 2019
Active Locations (4)
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1
CHU Besançon
Besançon, France, 25000
2
Centre Hospitalier de Dreux
Dreux, France, 28102
3
Hôpital Tenon
Paris, France, 75020
4
Hôpital Foch
Suresnes, France, 92151