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Clinical Trial Details — Status: Terminated

Administrative data

NCT number NCT00477347
Other study ID # 2006/37
Secondary ID
Status Terminated
Phase Phase 4
First received May 21, 2007
Last updated September 22, 2016
Start date May 2007
Est. completion date September 2009

Study information

Verified date September 2016
Source Hopital Foch
Contact n/a
Is FDA regulated No
Health authority France: Afssaps - Agence française de sécurité sanitaire des produits de santé (Saint-Denis)
Study type Interventional

Clinical Trial Summary

To compare closed-loop anesthesia to manual administration of propofol and remifentanil during liver transplantation


Description:

The Bispectral Index (BIS) is an electroencephalogram-derived measure of anesthetic depth. We hypothesized that BIS can also indicate the adequacy of analgesia. Therefore we built a combined closed-loop anesthesia system using BIS as control variable and two proportional-differential control algorithms, a propofol and a remifentanil target-controlled infusion system. The effectiveness of such a closed-loop anesthesia system has been demonstrated in a prospective, randomized study.

Elimination of anesthetic agents, propofol in particular, is strongly reduced during liver transplantation. Closed-loop anesthesia could provide adequacy for requirements in respect to the various phases of transplantation. Two groups of patients are compared: one in which propofol and remifentanil are administered by the anesthesiologist, using target-controlled infusion systems, and one in which propofol and remifentanil are administered automatically by the combined closed-loop anesthesia system. In both groups the goal is to maintain BIS between 40 and 60, the range recommended by the manufacturer during anesthesia. We expect the combined closed-loop anesthesia system group to do better: i.e. diminished consumption of propofol (primary outcome measure).


Recruitment information / eligibility

Status Terminated
Enrollment 5
Est. completion date September 2009
Est. primary completion date September 2009
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- liver transplantation

Exclusion Criteria:

- pregnant women

- allergy to propofol or remifentanil,

- neurological or muscular disorder,

- liver encephalopathy,

- patients taking psychotropic agents

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Subject), Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Device:
Closed loop administration
intraoperative closed loop administration of propofol and remifentanil
Manual administration
intraoperative manual administration of propofol and remifentanil

Locations

Country Name City State
France Dept of Anesthesia and Intensive Care, Hôpital Beaujon Clichy
France Dept of Anesthesia and Intensive Care, Hôpital H. Mondor Créteil

Sponsors (1)

Lead Sponsor Collaborator
Hopital Foch

Country where clinical trial is conducted

France, 

References & Publications (1)

Liu N, Chazot T, Genty A, Landais A, Restoux A, McGee K, Laloë PA, Trillat B, Barvais L, Fischler M. Titration of propofol for anesthetic induction and maintenance guided by the bispectral index: closed-loop versus manual control: a prospective, randomized, multicenter study. Anesthesiology. 2006 Apr;104(4):686-95. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary consumption of propofol during anesthesia maintenance during anesthesia maintenance No
Secondary - consumption of remifentanil - target modifications - hemodynamic events - volume loading and transfusion - extubation time, explicit memorization - time passed at BIS between 40 and 60 - MDAPE, wobble - global score - dysfunction of each system. during anesthesia maintenance No
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