New registry tracks stroke patients on ventilators to predict long-term outcomes
NCT ID NCT03335995
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study followed 364 adults with severe stroke who needed a breathing machine in the ICU. Researchers measured their recovery and disability levels at 3 months and 1 year after ICU admission. The goal was to better understand what happens to these patients over time, not to test a new treatment.
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Study facts
What this study's own registry entry says, in plain language.
- Participants
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364 people
The number who actually took part.
- Started
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Oct 2017
- Finished
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Nov 2020
- Lead sponsor
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A government agency
The lead sponsor is a government body.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
The subjects included in this study are adult patients requiring invasive mechanical ventilation at the acute phase of stroke (within 7 days of stroke onset), irrespective of indication for intubation. Prolonged mechanical ventilation of several days to weeks in ICU may be required for some patients, with various ICU discharge trajectories in survivors.
- Ages
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18 to 85 years
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion criteria: * Age\>18 years * Acute stroke (acute ischaemic stroke, brain hemorrhage, subarachnoid hemorrhage). The stroke diagnosis date is defined by the date of the initial brain imaging (TDM or MRI). * Admitted to ICU within 7 days before or after the diagnosis of stroke. * Requiring invasive mechanical ventilation in ICU for more than 24 hours. Exclusion criteria: * Traumatic causes of stroke * Refusal of the patient, or his reliable person, to participate in the study. * Privation of liberty by administrative or judicial decision
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Bichat Hospital
Paris, 75018, France
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Other studies related to the condition(s) this trial covers.
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