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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03757546
Other study ID # GIVRE
Secondary ID
Status Completed
Phase
First received
Last updated
Start date December 3, 2018
Est. completion date April 14, 2019

Study information

Verified date February 2020
Source Poitiers University Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The purpose of this study is to describe extra-pulmonary clinical manifestations of Influenza virus and Respiratory Syncitial Virus infections in hospitalized adults at a French university hospital.


Description:

Influenza virus and Respiratory Syncitial Virus (RSV) could be responsible for severe infections. Although flu was primarily considered as limited to the respiratory system, clinical reports suggest its association with organ involvement outside of the respiratory tract.

The aim of the study is to describe extra-pulmonary complications due to influenza virus and RSV in hospitalized patients from November 2018 to April 2019 and November 2019 to April 2020 in a French university hospital.


Recruitment information / eligibility

Status Completed
Enrollment 252
Est. completion date April 14, 2019
Est. primary completion date March 14, 2019
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Hospitalized adults =18 years old

- Flu or RSV infection confirmed by multiplex qPCR on nasal swab

- Oral non-opposition

Exclusion Criteria:

- No health insurance

- Co-infection with viruses other than influenza or RSV

Study Design


Intervention

Other:
observational
The aim of the study is to describe extra-pulmonary complications due to influenza virus and RSV in hospitalized patients from November 2018 to April 2019 and November 2019 to April 2020 in a French university hospital.

Locations

Country Name City State
France CHU de Poitiers Poitiers

Sponsors (1)

Lead Sponsor Collaborator
Poitiers University Hospital

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Evaluation frequency of extra-respiratory manifestations with clinical, biological and radiological data Clinical data (clinical examination)
Biological Data (blood test)
Radiological data
at 1 month
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