Functional Outcome After Cardiac Arrest

NCT ID: NCT02292147

Last Updated: 2020-08-19

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

140 participants

Study Classification

OBSERVATIONAL

Study Start Date

2013-03-13

Study Completion Date

2017-10-20

Brief Summary

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Descriptive and prognosis study of the functional outcome after cardiac arrest for the patients awake within the first 15 days.

Detailed Description

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Functional outcome after cerebral anoxia due to cardiac arrest is poorly documented.. Survival after out of hospital cardiac arrest has improved and long term follow up of the patients is not routinely effective. Patients showing sign of awakening very early are considered in a good outcome group. Nevertheless they can experience some restriction and difficulties when they try to return to their premorbid level of functioning.

We aim to study their long term functional outcome and their level of anxiety, depression, quality of life and caregiver burden as well as their general cognitive functioning. Prognosis factors will be studied in the acute phase.

Conditions

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Out of Hospital Cardiac Arrest

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Eligibility Criteria

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Inclusion Criteria

* age 18 to 85
* Out of hospital cardiac arrest ; cardiac arrest in the ER is eligible
* Glasgow Coma Score ≥ 12 within 15 days after onset
* Living in the parisian area

Exclusion Criteria

* no social security
* Neurological condition (multiple sclerosis, parkinson disease, AMS, stroke) priori to the cardiac arrest
* Psychiatric condition (schizophrenia, severe bipolar syndrome, long term neuroleptic medication, autistic spectrum disorders
* Deafness and blindness
* Neoplasia
* Premorbid limitation of autonomy.
* Difficulties in speaking and writing the French language
Minimum Eligible Age

18 Years

Maximum Eligible Age

85 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Assistance Publique - Hôpitaux de Paris

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Anne Peskine, MD

Role: STUDY_DIRECTOR

Assistance Publique - Hôpitaux de Paris

Charles-Edouard Luyt, MD, PhD

Role: PRINCIPAL_INVESTIGATOR

Assistance Publique - Hôpitaux de Paris

Locations

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Pitié salpetriere Hospital

Paris, , France

Site Status

Countries

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France

References

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Peskine A, Cariou A, Hajage D, Deye N, Guerot E, Dres M, Sonneville R, Lafourcade A, Navarro V, Robert H, Azouvi P, Sharshar T, Bayen E, Luyt CE; Hanox Study Group. Long-Term Disabilities of Survivors of Out-of-Hospital Cardiac Arrest: The Hanox Study. Chest. 2021 Feb;159(2):699-711. doi: 10.1016/j.chest.2020.07.022. Epub 2020 Jul 20.

Reference Type RESULT
PMID: 32702410 (View on PubMed)

Other Identifiers

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P111012

Identifier Type: -

Identifier Source: org_study_id

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