Decannulation of Tracheostomy Cannula Based on Suctioning Frequency and High-flow Oxygen Protocol in the Intensive Care Unit

NCT ID: NCT05778682

Last Updated: 2023-03-21

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

UNKNOWN

Clinical Phase

NA

Total Enrollment

50 participants

Study Classification

INTERVENTIONAL

Study Start Date

2023-03-20

Study Completion Date

2025-02-01

Brief Summary

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In the DECAP-ICU trial, the investigators will be focusing on the impact of a new weaning tracheostomy technique based on suctioning frequency compared to the standard practice of capping tolerance.

Detailed Description

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Conditions

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Tracheostomy Weaning

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

None, patients and physicians will know the protocol

Study Groups

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Suction based protocol

Weaning protocol based on suctioning frequency. Once the weaning of mechanical ventilation, the patients in this arm will be on high-flow nasal canula. The canula will be remove if the decannulation conditions are met (if the patient require less than 2 aspirations in 8 hours for 24 consecutive hours)

Group Type EXPERIMENTAL

Suctioning based protocol

Intervention Type PROCEDURE

cf. arm The necessity of suctioning will be assed continuously by the nurses, respiratory therapist and the medical team. If the patient require 2 or less aspiration each 8 hours for 24 hours straight, an attempt of decanalution will be done.

Usual care

Usual care will mainly base on the capping trial.

Group Type OTHER

Usual Care

Intervention Type PROCEDURE

Usual care in our center is tolerance to a capping trial.

Interventions

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Suctioning based protocol

cf. arm The necessity of suctioning will be assed continuously by the nurses, respiratory therapist and the medical team. If the patient require 2 or less aspiration each 8 hours for 24 hours straight, an attempt of decanalution will be done.

Intervention Type PROCEDURE

Usual Care

Usual care in our center is tolerance to a capping trial.

Intervention Type PROCEDURE

Eligibility Criteria

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Inclusion Criteria

* Weaning from mechanical ventilation for at least 24 hours
* Randomisation must be done in 24 hours of the mechanical ventilation weaning.

Exclusion Criteria

* Sabadell \> 2
* Contraindication of decannulation : Glasgow Coma Scale \<6, severe dysphagia, non permeable respiratory tracks, neuromuscular disease (expect for the ICU weakness) and long term tracheostomy.
Minimum Eligible Age

18 Years

Maximum Eligible Age

100 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Université de Sherbrooke

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Locations

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Université de Sherbrooke

Sherbrooke, Quebec, Canada

Site Status

Countries

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Canada

Facility Contacts

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Karl Courchesne

Role: primary

8199435275

Brian Grondin-Beaudoin

Role: backup

References

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Other Identifiers

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2022-4213

Identifier Type: -

Identifier Source: org_study_id

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