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NCT01032226 Clinical Trial

Evaluation of CNAP During Anesthesia

General Anesthesia Clinical Trial

— CnapEval  

Official title:
Evaluation of CNAP During Induction and Maintenance of General Anesthesia

Clinical Trial Details — Status: Terminated

Administrative data
NCT number NCT01032226
Other study ID # 2009/03
Secondary ID
Status Terminated
Phase N/A
First received December 12, 2009
Last updated September 22, 2016
Start date December 2009
Est. completion date March 2011

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 Observational

Clinical Trial Summary

The purpose of this study is to compare

- the non invasive measurement of arterial pressure (CNAP monitor)

- with the invasive measurement of arterial pressure (radial artery catheter) during induction and maintenance of general anesthesia

Recruitment information / eligibility
Status Terminated
Enrollment 45
Est. completion date March 2011
Est. primary completion date March 2011
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Age >18

- ASA II, III or IV

- weight between 40 and 180 kg; BMI < 35

- surgical procedure performed in supine position

- normal Allen's test and hand Doppler examination.

Exclusion Criteria:

- cardiac arrhythmias,

- history of vascular surgery or vascular implant in the upper limb

Study Design

Observational Model: Cohort, Time Perspective: Prospective

Related Conditions & MeSH terms

Locations
Country Name City State
France Hôpital Foch Suresnes

Sponsors (1)
Lead Sponsor Collaborator
Hopital Foch

Country where clinical trial is conducted

France, 

Outcome
Type Measure Description Time frame Safety issue
Primary Comparison between both methods of arterial pressure measurement intraoperative No
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