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COVID-19TOCCIPNCT04433325

COVID-19 Critically Ill Patients' Evolution After Medical Transport by Train From Paris Intensive Care Units to West of France Intensive Care Units

An observational study of COVID-19 and Intensive Care Unit Syndrome, run by Rennes University Hospital at 2 sites in France.

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

Since early 2020, France knows a sanitary crisis with a massive influx of COVID-19 patients admitted in Intensive Care Units (ICU). It led to a saturation of the French health system, especially in some geographic areas such as East of France or Paris region. Read more about this study

Who is it for?
Ages 18 years and older
Conditions the study is for
COVID-19, Intensive Care Unit Syndrome
How many people
37 participants
Where
2 sitesFrance
Study dates
30 Jul 2020to 6 Oct 2020
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 years and older
  • All sexes
  • Adult, Older adult

Study population: COVID-19 positive patients admitted in Intensive Care Unit between 15/03/2020 and 15/04/2020

Who may be able to join

  • Age > 18 years
  • COVID-19 positive patients admitted in Intensive Care Unit between 15/03/2020 and 15/04/2020
  • Patients (or legal representative) with no opposition to inclusion in medical research protocol
  • Regarding case group : Patients transferred from Paris's ICU
  • Regarding case control group : Patients admitted in ICU with no transfer from Paris

Who cannot join

  • > 18 years under legal protection and patients with liberty restriction

Trial locations and contacts

2 sites in 1 country.

France2 sites
  • CHU Poitiers

    Poitiers

  • CHU Tours

    Tours

Other trials in France

About this study

Since early 2020, France knows a sanitary crisis with a massive influx of COVID-19 patients admitted in Intensive Care Units (ICU). It led to a saturation of the French health system, especially in some geographic areas such as East of France or Paris region. Therefore, authorities decided to transfer some critically ill patients from these crowded ICUs to less busy regional ICUs. it was done for the first time by medical train transportation. Knowing that the investigators lack experience regarding this type of medical evacuation, regarding the high number of transferred patients, with such a logistic effort, the investigators decided to study this phase of the COVID-19 sanitary crisis in order to draw a feedback. So far, there are no data in the literature regarding this topic.

Keywords
Medical transport by train
Medical subject headings
COVID-19

What participants receive

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

Study groups in NCT04433325
Study groupRoleWhat they receive
Patients transferredPatients transferred from Paris's Intensive Care Units
Patients not transferredPatients admitted in Intensive Care Units with no transfer from Paris

What is being measured

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

  1. number of death

    to evaluate mortality

    Measured: at Intensive Care Units discharge, an average of 1 months

Secondary outcomes (7)
  1. number of infections

    to evaluate morbidity

    Measured: from date of admission until Intensive Care Units discharge, assessed up to 1 months

  2. number of days of mechanical ventilation

    Measured: from date of admission until Intensive Care Units discharge, assessed up to 1 months

  3. number of days of sedation

    Measured: from date of admission until Intensive Care Units discharge, assessed up to 1 months

  4. number of days of use of neuromuscular blocking agents

    Measured: from date of admission until Intensive Care Units discharge, assessed up to 1 months

  5. number of days of vasopressor use

    Measured: from date of admission until Intensive Care Units discharge, assessed up to 1 months

  6. number of days in Intensive Care Units

    Measured: from date of admission until Intensive Care Units discharge, assessed up to 1 months

  7. number of days in hospital

    Measured: from date of admission until hospital discharge, assessed up to 1 months

Timeline

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

  1. First posted16 Jun 2020
  2. Study start30 Jul 2020
  3. Primary completion6 Aug 2020
  4. Study completion6 Oct 2020

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
Case-control
Time perspective
Retrospective
Enrolment
37 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT04433325
Sponsor's protocol ID
35RC20_3091_TOCCIP
Acronym
TOCCIP
Status last verified
Jun 2026
First submitted
12 Jun 2020
Last updated
12 Jun 2026
Results posted
No
FDA-regulated drug
No
FDA-regulated device
No

Questions about this trial

What is this clinical trial studying?

An observational study of COVID-19 and Intensive Care Unit Syndrome, run by Rennes University Hospital at 2 sites in France.

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 5 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 12 Jun 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 2 sites in France. Whether a site is taking part right now should be confirmed with that site. See every site.

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?

number of death (time frame: at Intensive Care Units discharge, an average of 1 months). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
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 12 Jun 2026.

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