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One-year Outcomes in Survivors of the Severe COVID-19 Pneumonia (CO-Qo-ICU)

C

Centre Hospitalier Universitaire de Nice

Status

Enrolling

Conditions

Quality of Life
COVID
ARDS

Study type

Observational

Funder types

Other

Identifiers

NCT04401111
20reamedcovid04

Details and patient eligibility

About

Many of the patients hospitalized for a severe form of SARSCoV-2 respiratory impairment require prolonged intensive care that can be complicated in the short term, In the medium and long term, physical and psychological sequelae can affect patients' quality of life and prevent a return to normal working life.

To date, there is little data on the fate of patients treated in Resuscitation for a severe form of COVID-19, both in terms of respiratory sequelae, as well as in terms of psychological sequelae and their quality of life. The objective of this study is to be able to describe and evaluate the possible physical and psychological sequelae and quality of life of patients hospitalized in Resuscitation for a severe form of COVID-19 in the short (3 and 6 months), medium (1 year) and long (5 years) End of their stay in ICU. To do this, we want to carry out a prospective, observational and monocentric study in the consultation department of the Nice CHU. All patients admitted to Resuscitation for a severe form of COVID-19 who have accepted the longitudinal medical follow-up proposed by the Nice CHU will be included in the study and data from the computerized medical record will be analyzed.

Enrollment

150 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria:

  • Patients hospitalized in ICU for an ARDS table
  • PCR SARSCoV-2 nasopharyngeal or positive pulmonary samples

Trial design

150 participants in 1 patient group

Survivors of Intensive care unit patients
Description:
Survivors of severe COVID-19 pneumonia after intensive care unit

Trial contacts and locations

1

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Central trial contact

Clément SACCHERI; Jean DELLAMONICA, MD, PhD

Data sourced from clinicaltrials.gov

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