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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04439604
Other study ID # NOWOBILSKI 2019
Secondary ID
Status Completed
Phase
First received
Last updated
Start date October 6, 2018
Est. completion date December 6, 2019

Study information

Verified date June 2020
Source Centre Hospitalier Universitaire Dijon
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The induction of general anaesthesia is associated with a fall in lung volume due in particular to a decrease in muscle tone and the formation of denitrogenation atelectasis. Many recent studies insist on the need to apply a so-called "protective" strategy of intraoperative ventilation, which combines the use of recruitment manoeuvres, reduced tidal volume (Vt) (6-8ml/kg) and positive expiratory pressure (PEEP) to prevent these phenomena. However, the setting of PEEP remains debated and several authors agree on the need to individualize ventilatory parameters, particularly in obese patients, without describing the individualization tools.

In the ICU, it has been shown that electrical impedance tomography (EIT) can be used to individualise the PEEP level in a simple and non-invasive way. Therefore, we wish to determine whether the use of this technique during general anaesthesia allows for the individualization of PEEP, and whether the value determined is correlated with the body mass index (BMI).


Recruitment information / eligibility

Status Completed
Enrollment 59
Est. completion date December 6, 2019
Est. primary completion date July 6, 2019
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Adult patient

- Patient who received general anesthesia with orotracheal intubation.

- Patient who has undergone surgery of the following types: : abdominal surgery by laparotomy or laparoscopy, emergency or scheduled

Exclusion Criteria:

- NA

Study Design


Related Conditions & MeSH terms


Intervention

Other:
regional ventilation monitoring
regional ventilation monitoring

Locations

Country Name City State
France Chu Dijon Bourgogne Dijon

Sponsors (1)

Lead Sponsor Collaborator
Centre Hospitalier Universitaire Dijon

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary electrical impedance tomography Through study completion, an average of 1 year
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