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Efficacy of an Early Rehabilitation on Decannulation Time of Patients With Severe Acquired Brain Injury | Clinical Trials | Clareo Health

UNKNOWN

Efficacy of an Early Rehabilitation on Decannulation Time of Patients With Severe Acquired Brain Injury

NCT02990871•Ospedale Generale Di Zona Moriggia-Pelascini

View on ClinicalTrials.gov

Summary

All the patients hospitalized in the neuro-rehabilitation after a severe acquired brain injury carrying a tracheal cannula will be retrospectively analyzed. Patients coming from emergency department started a rehabilitative treatment during their hospitalization in ICU. Patients transferred from an external ICU started the rehabilitation in neurorehabilitation department. Aim of the study is to evaluate if an early rehabilitation, started since the acute stage of the damage, is able to reduce the decannulation time in this group of patients.

Eligibility

Age

18 - No limit years

Sex

ALL

Healthy Volunteers

Inclusion Criteria

•presence of a tracheostomy at admission in NRehab
•patient moved from an ICU
•GCS≤11 at admission in ICU
•tracheostomy performed for decreased mental status due to the ABI,

Exclusion Criteria

•tracheostomy performed prior to admission to the ICU
•need for ventilation support.

Locations (1)

Ospedale Generale di Zona Moriggia Pelascini

Gravedona Ed Uniti, CO, Italy

Key Dates

Start Date

May 1, 2016

Primary Completion Date

October 1, 2016

Last Updated

December 22, 2016

Enrollment

ESTIMATED participants

Conditions

Brain InjuryTracheostomyNeurological Rehabilitation

Interventions

early neurological rehabilitation

OTHER

no-early neurological rehabilitation

OTHER

Clinical Randomisation of an Anti-fibrinolytic in Symptomatic Mild Head Injury in Older Adults

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Traumatic Brain Injury

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RECRUITING

A Study to Develop a Blood-based Test for Aiding the Diagnosis/Prognosis of Traumatic Brain Injury in Adults and for Monitoring the Development of Secondary Events in Patients Diagnosed With Traumatic Brain Injury

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Traumatic Brain Injury

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RECRUITING

Hemodynamic ABI Monitor

Data Source & Attribution

This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.

ClinicalTrials.gov last update: December 22, 2016Data synced to Clareo: March 29, 2026

Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.

Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.

View ClinicalTrials.gov Terms and Conditions

Efficacy of an Early Rehabilitation on Decannulation Time of Patients With Severe Acquired Brain Injury

Inclusion Criteria

Exclusion Criteria

Clinical Randomisation of an Anti-fibrinolytic in Symptomatic Mild Head Injury in Older Adults

A Study to Develop a Blood-based Test for Aiding the Diagnosis/Prognosis of Traumatic Brain Injury in Adults and for Monitoring the Development of Secondary Events in Patients Diagnosed With Traumatic Brain Injury

Hemodynamic ABI Monitor

Multimodal, Enriched Environment for Rehabilitation in Chronic Traumatic Brain Injury

Carbon Dioxide Administration and Brain Waste Clearance

PRophylaxis Against Early VENTilator-associated Infections in Acute Brain Injury