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NutriCovid30 : Nutritional Evaluation for Covid-19 Infection at D30

Grenoble Alpes University Hospital Center (CHU) logo

Grenoble Alpes University Hospital Center (CHU)

Status

Completed

Conditions

COVID-19

Treatments

Other: Interview

Study type

Observational

Funder types

Other

Identifiers

NCT04365816
2020-A01120-39

Details and patient eligibility

About

Describe the main clinical features impacting the food intake, and therefore the nutritional status of a population infected by a coronavirus.

Full description

The recent Covid-19 outbreak has brought USA, European, British and French nutrition learned societies to publish recommendations for the nutritional management of patients infected with the SARS-CoV-2. They reminded that there is a risk of malnutrition for that population.

The emergency and rapid evolution in the situation have led to severe cases of anosmia, ageusia, diarrhea, odynophagia, anorexia etc.. Some of the first patients cured from Covid-19 have lost up to 10 kgs.

To this day, there is no available information regarding either nutritional characteristics or nutritional interventions (enteral or parenteral nutrition, oral nutritional supplements, dietary supplementations) for Covid-19 patients.

The objective of this study is to describe nutritional consequences of the Covid-19 infection for adults, 30 days after their discharge from hospital, as well as the nutritional care they received.

Type and proportion of chronic diseases will be assessed in this trial.

Enrollment

403 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • 30 days or more after discharge from hospital for Covid-19
  • Patient received information about the trial and gave his/her consent
  • Patient capable of answering the phone (alone or with some help)

Exclusion criteria

  • Patient diseased
  • impossibility to collect information from the patient or one of his/her relatives
  • Patient protected by the French Public Health Code (art. L1121-5 à L1121-8)

Trial design

403 participants in 7 patient groups

Prospective cohort University Hospital, Grenoble
Description:
Semi-structured survey administered on the phone, once, one month after discharge from hospital. The interview will not be recorded.
Treatment:
Other: Interview
Prospective cohort University Hospital, Toulouse
Description:
Semi-structured survey administered on the phone, once, one month after discharge from hospital. The interview will not be recorded.
Treatment:
Other: Interview
Prospective cohort University Hospital, Nancy
Description:
Semi-structured survey administered on the phone, once, one month after discharge from hospital. The interview will not be recorded.
Treatment:
Other: Interview
Prospective cohort University Hospital, Rennes
Description:
Semi-structured survey administered on the phone, once, one month after discharge from hospital. The interview will not be recorded.
Treatment:
Other: Interview
Prospective cohort Hospices Civils de Lyon
Description:
Semi-structured survey administered on the phone, once, one month after discharge from hospital. The interview will not be recorded.
Treatment:
Other: Interview
Prospective cohort Assistance Publique Hôpitaux de Paris
Description:
Semi-structured survey administered on the phone, once, one month after discharge from hospital. The interview will not be recorded.
Treatment:
Other: Interview
Prospective cohort University Hospital, Rouen
Description:
Semi-structured survey administered on the phone, once, one month after discharge from hospital. The interview will not be recorded.
Treatment:
Other: Interview

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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