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Intensive Care Units (ICUs)FRANSNCT02599948

FRench-speAking Icu (Intensive Care Unit) Nutritional Survey

An observational study of Intensive Care Units (ICUs), run by Assistance Publique - Hôpitaux de Paris.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

Assessment of nutritional practices in french intensive care units. Read more about this study

Who is it for?
Ages 18 to 99 years
Conditions the study is for
Intensive Care Units (ICUs)
How many people
1,215 participants
Where
No sites listed yet
Study dates
Mar 2015to Sep 2015
Phase
Observational
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 99 years
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Study population: Adults hospitalized patients in ICU

Who may be able to join

  • Adults hospitalized patients in intensive care units for an expected period of stay> 3 days

Who cannot join

  • Refuse to participate in the Protocol

About this study

Assessment of nutritional practices in french intensive care units.

Read the detailed description

Assessment of nutritional practices in french intensive care units.

Being tested
no intervention

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • no interventionOther

Study groups in NCT02599948
Study groupRoleWhat they receive
Patients hospitalised in ICUPatients hospitalised in ICU
Receives: Other: no intervention

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Frequency of patients receiving parenteral nutrition within the first 10 days after ICU admission

    Measured: 10 days

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted9 Nov 2015 (estimated)
  2. Study startMar 2015
  3. Primary completionSep 2015
  4. Study completionSep 2015

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Other
Time perspective
Prospective
Enrolment
1,215 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT02599948
Sponsor's protocol ID
IRB00003835
Acronym
FRANS
Status last verified
Aug 2014
First submitted
3 Nov 2015
Last updated
3 Feb 2023
Results posted
No
Data monitoring committee
No

Publications

  • Pardo E, Lescot T, Preiser JC, Massanet P, Pons A, Jaber S, Fraipont V, Levesque E, Ichai C, Petit L, Tamion F, Taverny G, Boizeau P, Alberti C, Constantin JM, Bonnet MP; FRANS study group. Association between early nutrition support and 28-day mortality in critically ill patients: the FRANS prospective nutrition cohort study. Crit Care. 2023 Jan 7;27(1):7. doi: 10.1186/s13054-022-04298-1.

    PubMed 36611211

Questions about this trial

What is this clinical trial studying?

An observational study of Intensive Care Units (ICUs), run by Assistance Publique - Hôpitaux de Paris.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 1 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 3 Feb 2023. Status can change between updates, so confirm with the study contact before making plans.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Frequency of patients receiving parenteral nutrition within the first 10 days after ICU admission (time frame: 10 days). It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT02599948, which also lists 1 linked publication.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 3 Feb 2023.

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