Measuring Diaphragm Electrical Activity in Neonates Using a Smaller Inter-electrode Distance

StatusActive, Not Recruiting
PhaseNot applicable
Started

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Record History

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  1. Minor Study completion pushed from Jun 2026 to Jan 2027
    • Eligibility criteria expanded, about 5 words
  2. Minor Study completion date: Aug 2025 to Jun 2026v12
  3. Minor Study completion date: Mar 2025 to Aug 2025v11
  4. Minor Study completion date: Nov 2024 to Mar 2025v10
  5. Minor Study completion date: Sep 2024 to Nov 2024v9
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  1. Minor Trial status: Recruiting to Active, Not Recruiting
    • Primary completion date changed from estimate of Apr 2024 to Jul 10, 2024
    • Study completion date: Jun 2024 to Sep 2024
    • Site details revised
    v8
  2. Minor Primary completion date: Dec 2023 to Apr 2024
    • Study completion date: Feb 2024 to Jun 2024
    v7
  3. Minor Eligibility criteria revisedv6
  4. Notable Primary completion date: Dec 2022 to Dec 2023
    • Study completion date: Feb 2023 to Feb 2024
    • Start date changed from estimate of Oct 2022 to Jan 12, 2023
    v5
  5. Notable Start date: Aug 2022 to Oct 2022v4
  6. Notable Trial status: Not Yet Recruiting to Recruiting
    • Start date: Jul 2022 to Aug 2022
    • Site details revised
    v3
  7. Minor Start date: Aug 2022 to Jul 2022
    • Study description expanded, about 1 word
    • Study title shortened, about 4 words
    v2
  1. Minor Study First Submitted
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
Neurally Adjusted Ventilatory Assist (NAVA) is a mode of ventilation where the electrical activity of the diaphragm (EDI) - a signal representing the baby's respiratory drive - is used to control the timing and amount of assist provided. NAVA was introduced to the market in 2007 and since has been used in more than 40 countries. In the current clinical practice, the Edi signal from the patient is captured with miniature sensors (the size of a hair) embedded in the wall of a specially designed naso/orogastric feeding tube. This FDA and Health Canada approved, commercially available catheter (Getinge, Solna, Sweden), is 6 Fr in size (outer diameter), 49 cm in length and has 8 pairs of sensors that are placed 6 mm apart (so-called inter electrode distance (IED) is 6 mm). While no obvious side effects have been noted by clinicians, for the smallest of neonates, the currently used commercial catheter (size 6F, 49 cm long) may have 'excessive' post-array catheter length. In these neonates, typically those with weight \< 1000 grams, following the correct placement of catheter as per the electrode array positioning at gastro-esophageal junction, the feeding holes in the catheter may end at the level of distal stomach instead of the desirable mid-stomach location. The changing demographics of the patients in the Neonatal Intensive Care Units (NICU) has created a clinical need to redesign the currently used Edi catheter specifically to suit the smallest of patients, such that following adequate placement the feeding holes sit at the level of mid-stomach. Drs. Christer Sinderby and Jennifer Beck in Toronto, Canada, are the original designers of the 6 mm/49 cm currently used Edi catheter. These investigators (at St-Michael's Hospital, Toronto) in collaboration with their team at Neurovent Research Inc. (NVR) have re-designed and invented a new prototype of the current FDA-approved catheter specifically suited for use in extreme premature neonates. They have done so by reducing the interelectrode distance from the originally set 6 mm to 4 mm, which reduces the overall insertion depth to capture the same signal from the diaphragm. All other parameters are exactly same as the original catheter (6F, 49 cm long). In this small feasibility study the investigators wish to provide a clinical proof of concept for the use of this newly designed prototype in 10 extremely premature neonates who are already receiving NAVA ventilation in the NICU.
Trial Details
NCT Number NCT05427929
Lead Sponsor Mount Sinai Hospital, Canada
Collaborators: Unity Health Toronto
Conditions
(from sponsor)
Respiratory Distress Syndrome, Newborn, Infant, Premature
Related terms Premature Birth, Respiratory Distress Syndrome, Newborn
Enrollment 10 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov