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Assessement of Viral Shedding Duration After a Respiratory Tract Infection in Oncology and Hematology Patients (ONCOVIR)

P

Poitiers University Hospital

Status

Completed

Conditions

Respiratory Tract Viral Infection

Treatments

Diagnostic Test: nasal swabs

Study type

Interventional

Funder types

Other

Identifiers

NCT03389997
ONCOVIR

Details and patient eligibility

About

The purpose of this study is to assess the duration of the viral shedding in hematology and oncology patients after a respiratory tract viral infection. This duration has not been much studied in that population whereas it is probably longer than that in immunocompetent patients. Thereby it may be a source of transmission amongst these immunocompromised patients.

Full description

The development of multiplex polymerase chain reaction (PCR) tests has greatly improved the diagnosis of respiratory tract viral infections by increasing its sensitivity and the diversity of viral species detected. However, there are few data concerning respiratory tract viral infections amongst hematology and oncology patients. Especially, the duration of viral shedding following an infection has not been much studied whereas it is a source of inter-individual transmission between immunocompromised patients who are more likely to develop severe disease.

Studies conducted so far concerned mainly hematology patients. They have shown that viral carriage could last up to one month and a half in some patients with hematological malignancy.

The aim of this study is to determine the duration of the viral shedding in patients from hematology and oncology units after a respiratory tract viral infection for the ten main viruses involved in order to better manage these infections and to better prevent their transmission.

Enrollment

44 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patient with solid organ cancer or haematological malignancy with or without chemotherapy
  • Having symptoms of upper and/or lower respiratory tract infection
  • Virus detected by PCR in nasal sample
  • Signature of consent

Exclusion criteria

  • Hematological stem cell and solid organ recipients
  • No health insurance
  • protected people

Trial design

Primary purpose

Prevention

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

Trial contacts and locations

1

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Central trial contact

Joseph Raphael; Andy LARIVIERE, residents

Data sourced from clinicaltrials.gov

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