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Factors Influencing Anesthetic Drug Requirement (PosoAnes)

H

Hopital Foch

Status

Completed

Conditions

Anesthesia, General

Treatments

Device: Closed loop anesthesia

Study type

Interventional

Funder types

Other

Identifiers

NCT00896714
2008/44

Details and patient eligibility

About

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 drug requirements (hypnotic and opiate).

Enrollment

3,278 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients undergoing scheduled surgery under general anesthesia, agreeing to participate in the study

Exclusion criteria

  • 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

Trial design

Primary purpose

Treatment

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

3,278 participants in 1 patient group

Closed loop anesthesia
Experimental group
Treatment:
Device: Closed loop anesthesia

Trial contacts and locations

4

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Data sourced from clinicaltrials.gov

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