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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT03108430
Other study ID # RNI2016-10
Secondary ID
Status Recruiting
Phase N/A
First received March 31, 2017
Last updated April 5, 2017
Start date August 22, 2016
Est. completion date August 21, 2017

Study information

Verified date April 2017
Source Centre Hospitalier Universitaire, Amiens
Contact Jean-Philippe LANOIX, Dr
Email lanoix.jean-philippe@chu-amiens.fr
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Inhalation pneumonia (PI) is common in clinical practice but is rarely studied. For example, there are no data on the incidence of pneumonia after inhalation and risk factors or protective factors to develop one since it is known that anyone who inhaled does not necessarily develop an IP. There is no data on the benefit of treating inhalation by antibiotic therapy pre-emptively although this practice is common. In this context, this observational study wishes to take stock of the situation on the subject in order to determine what actions to implement to prevent IP.


Recruitment information / eligibility

Status Recruiting
Enrollment 60
Est. completion date August 21, 2017
Est. primary completion date August 21, 2017
Accepts healthy volunteers No
Gender All
Age group N/A and older
Eligibility Inclusion Criteria:

- In intensive care: Any intubated patient who presented:

- It is a coma with GCS = 12 without VAS protection, whatever the duration

- Either a proven inhalation, defined by the presence in the VAS of gastric fluid or food

- Either a suspected inhalation, defined by the extrahospital anamnesis

- In medicine :

- Any wrong way (defined by a reflex cough when taking food)

- Coma without intubation, regardless of duration or depth

Exclusion Criteria:

- Patients with VAP

Study Design


Intervention

Other:
Risk factors and incidence of IP after inhalation
Calculate the annual incidence of PI, the incidence of PI in inhaled patients (in each subgroup), and analyze the risk factors by logistic regression, based on the number of patients hospitalized during the study period.

Locations

Country Name City State
France CHU Amiens Picardie Amiens Picardie

Sponsors (1)

Lead Sponsor Collaborator
Centre Hospitalier Universitaire, Amiens

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Calculate the annual incidence of PI, the incidence of PI in inhaled patients (in each subgroup), and analyze the risk factors by logistic regression, based on the number of patients hospitalized during the study period. 1 day
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