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Tracheal Suctioning With or Without Expiratory Pause Maneuver in Children

H

Hospital de Clinicas de Porto Alegre

Status

Completed

Conditions

Mechanical Ventilation Complication
Pediatric Respiratory Diseases

Treatments

Other: Endotracheal suctioning without expiratory pause
Other: Endotracheal suctioning with expiratory pause

Study type

Interventional

Funder types

Other

Identifiers

NCT05805475
2022-0072

Details and patient eligibility

About

The purpose of this study is to evaluate the efficacy of tracheal suctioning associate with expiratory pause maneuver in children on invasive mechanical ventilation.

Full description

After being informed about the study and potential risks, all parents or guardians giving written informed consent will be evaluate for study entry. Children in invasive mechanical ventilation who meet eligibility criteria will be submitted of two techniques of tracheal suctioning (with and without expiratory pause maneuver), randomized in a crossover trial in a 1:1 ratio, for determine the first technique to be applied.

Clinical data will be collected (sex, age, presence of previous disease, diagnosis of hospitalization), as well as the ventilatory parameters (ventilation mode, peak inspiratory pressure, positive end-expiratory pressure, tidal volume, respiratory frequency, fraction of inspired oxygen).

The protocol consists of an initial conventional tracheal suctioning with a negative pressure of 40mmHg for all the participants. After two (2) hours the first technique will be applied and an interval of another two hours for the application of the second technique. Respiratory mechanics and hemodynamic parameters will be evaluate before and after 30 minutes of each tracheal suctioning techniques.

In case of clinical alterations that may aggravate the patients condition during the protocol (oxygen saturation < 85%, heart rate > 190bpm and/or decrease 20% of mean arterial blood pressure), the technique will be interrupted immediately and the patient will be evaluated.

Enrollment

10 patients

Sex

All

Ages

1 month to 2 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Children at invasive mechanical ventilation for more than 24 hours;
  • Under the effect of neuromuscular blocker (level of sedation assessed using the Comfort B Scale with a score <10 and without a cough reflex);
  • Endotracheal suctioning in a period > 2h before the application of the technique.

Exclusion criteria

  • Patients with undrained pneumothorax or hemothorax, or presence of subcutaneous emphysema;
  • Hemodynamic instability (hypotension refractory to treatment)
  • Need of frequent endotracheal suctioning

Trial design

Primary purpose

Other

Allocation

Randomized

Interventional model

Crossover Assignment

Masking

Single Blind

10 participants in 2 patient groups

Endotracheal suctioning without expiratory pause
Active Comparator group
Description:
Conventional endotracheal suctioning in closed suction system
Treatment:
Other: Endotracheal suctioning without expiratory pause
Endotracheal suctioning with expiratory pause
Experimental group
Description:
Endotracheal suctioning in closed suction system associated with expiratory pause maneuver
Treatment:
Other: Endotracheal suctioning with expiratory pause

Trial contacts and locations

1

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Central trial contact

Bruna Ziegler; Ana Paula Peiter

Data sourced from clinicaltrials.gov

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