Transcutaneous PCO2 Assessment During Intubation in ICU

NCT ID: NCT03888430

Last Updated: 2019-10-28

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

202 participants

Study Classification

OBSERVATIONAL

Study Start Date

2018-05-17

Study Completion Date

2019-04-13

Brief Summary

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PtcCO2 assessement during intubation in ICU. Comparison of three different preoxygenation methods.

Detailed Description

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Transcutaneous PCO2 assessement during intubation in ICU. Comparison of three different preoxygenation methods and hemodynamic changes during this period.

Conditions

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Intubation in ICU

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Study Groups

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Standard Oxygen

preoxygenation methods : Standard Oxygen

PtcCO2 measure during intubation

Intervention Type PROCEDURE

Transcutaneous measure during intubation. Non invasive measure without any risk according to the literature

High flow Oxygen

preoxygenation methods : High flow Oxygen

PtcCO2 measure during intubation

Intervention Type PROCEDURE

Transcutaneous measure during intubation. Non invasive measure without any risk according to the literature

Non invasive ventilation

preoxygenation methods : Non invasive ventilation

PtcCO2 measure during intubation

Intervention Type PROCEDURE

Transcutaneous measure during intubation. Non invasive measure without any risk according to the literature

Interventions

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PtcCO2 measure during intubation

Transcutaneous measure during intubation. Non invasive measure without any risk according to the literature

Intervention Type PROCEDURE

Eligibility Criteria

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Inclusion Criteria

* Adult patient 18 years of age or older
* Requiring intubation in Resuscitation

Exclusion Criteria

* Contraindication to orotracheal intubation
* Intubation in a respiratory or cardiocirculatory arrest situation
* Need for intubation in great urgency preventing the installation of the transcutaneous capnia sensor and its calibration
* Major Incapable
* Opposition of the patient or his relatives to the research
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Rennes University Hospital

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Aurélien FREROU, MD

Role: PRINCIPAL_INVESTIGATOR

Rennes University Hospital

Locations

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Centre Hospitalier Universitaire de Rennes

Rennes, , France

Site Status

Countries

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France

Other Identifiers

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35RC18_3030_C-TOP

Identifier Type: -

Identifier Source: org_study_id

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