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Completed

NCT Number: NCT06163183

Does Diaphragm Electrical Activity Monitoring Predict Extubation Success in Children?

This study aimed to record diaphragm electrical activity (Edi) during the preextubation (weaning) and postextubation periods and to analyze whether Edi monitoring could predict extubation success.

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Key information

Age range

2 month–17 year

Sex eligibility

All sexes

Study type

Observational

About this study

This prospective observational study included 25 pediatric patients who were intubated due to respiratory failure in the pediatric intensive care unit of the tertiary university-affiliated Marmara University Hospital between August 2014 and July 2015. To conduct the study, we obtained informed consent from the patient's parents and ethical approval from the Marmara University Faculty of Medicine Scientific Research Ethics Committee Board on 06.09.2014. Pediatric patients included which had indication for the insertion of a nasogastric tube (Edi catheter), independent of the study. So Edi catheter had been used instead of nasogastric tube.

When the patients were ready for clinical weaning in accordance with the clinician, the Edi catheter was appropriately inserted into the patients. Then, a spontaneous breathing trial (SBT) was performed and diaphragm activity monitoring was recorded during this process. The patients who met the inclusion criteria switched in a spontaneous breath trial with pressure support ventilation (PSV) or NAVA (Neurally Adjusted Ventilatory Assist) on a Maquet (Solna, Sweden) Servo-i mechanical ventilator for both ventilation modes The patients' demographic and clinical characteristics, mortality scoring, vital parameters (HR, TA, SpO2, RR) and ventilatory parameters (Edi peak, Edi min, FiO2, expiratory Vt), as well as follow-up period were recorded. Arterial/capillary blood gases were taken within the last four hours before extubation and within the first, sixth, 12th, 18th and 24th hours after extubation. If arterial blood gas monitoring was initiated in the patient, arterial monitoring was continued. If capillary blood gas monitoring was initiated, capillary monitoring was continued. Edi data were recorded for at least 24 hours before and after extubation. Edi values were obtained retrospectively from the trend diagram, which provides 24-hour continuous records on the ventilator screen.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • • Aged between one month and 18 years old
  • Intubated for more than 48 hours due to respiratory failure
  • Indication for the insertion of a nasogastric tube (Edi catheter), independent of the study
  • Ready for weaning:
  • Normal vital signs for age (fever, heart rate (HR), respiratory rate (RR), tension arterial (TA)
  • No catecholamines or sedation drugs
  • pH of 7.35 to 7.45
  • Positive end expiratory pressure (PEEP) ≤6 mmHg
  • Fractionated oxygen (FiO2) ≤0.5
  • Oxygen saturation (SpO2) ≥92%
  • Vt≥ 5 ml/kg

Exclusion criteria

  • • Contraindication for the insertion of the nasogastric tube (Edi catheter)
  • Patients treated with muscle relaxants
  • Absence of consent given by the patient's family
  • Cases whose Edi levels could not be taken from ventilator's trend diagram due to missing values.

Treatment and study plan

Edi catheter

Device

Primary outcomes

  1. Diaphragm electrical activity (Edi) monitoring

    Time frame: up to 2 days

    Macquet (servo-i) mechanical ventilator measures the electrical activity (Edi) of the diaphragm (microvolts). Edi signals are measured using special feeding tubes (Edi catheter) equipped with tiny sensors at the level of gastroesophageal junction. In the ventilator, Edi trend values can be monitored continuously as 24-hour records.

  2. Mechanical ventilatory monitoring

    Time frame: up to 2 days

    ventilatory parameters (Edi peak, Edi min, FiO2), were recorded during the follow up.

Secondary outcomes

  1. Arterial/capillary blood gases

    Time frame: Arterial/capillary blood gases were taken within the last four hours before extubation and within the first, sixth, 12th, 18th and 24th hours after extubation.

    If arterial blood gas monitoring was initiated in the patient, arterial monitoring was continued. If capillary blood gas monitoring was initiated, capillary monitoring was continued.

  2. Vital signs ((fever, heart rate (HR), respiratory rate (RR), tension arterial))

    Time frame: up to 2 days

    Vital signs recorded by pediatric intensive care nurses.

  3. Expiratory tidal volume

    Time frame: From spontaneous breathing trial until the time for extubation

    Patients who had >5ml/kg expiratory tidal volume considered to be ready for extubation

Sponsors and collaborators

Lead sponsor

Mersin University

Other

Registry information

Official study title

The Potential of Diaphragm Electrical Activity Monitoring to Predict Extubation Success in Children Requiring Mechanical Ventilation Support Due to Respiratory Failure

Important dates

Study start
2014
Primary completion
2015
Study completion
2015
First posted
Dec 8, 2023
Registry last updated
Dec 8, 2023

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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