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NCT05759013 · ClinicalTrials.gov registry record · NA

Pivotal Evaluation of Abdominal Neuromuscular Electrical Stimulation (VentFree) for Weaning From Mechanical Ventilation

A NA study, sponsored by Liberate Medical.

Completed
Registry status
NA
Development phase
250
Enrollment target

NCT05759013: Completed NA study, sponsored by Liberate Medical.

NCT05759013 is a NA study that has completed, run by Liberate Medical. The registered enrollment target is 250 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (82% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT05759013, a NA study, has completed, sponsored by Liberate Medical.

COMPLETED
Registry status
NA
Development phase
250 participants
Enrollment target

Study Summary

The objective of this study is to evaluate the efficacy of the VentFree Respiratory Muscle Stimulator (VentFree) in critically ill adult patients who require invasive mechanical ventilation, when compared to sham.

Primary Outcome

Successful liberation is defined as disconnection from mechanical ventilation that does not require invasive mechanical ventilation in the subsequent 7 days after disconnection, or until ICU discharge, or until live hospital discharge, whichever occurs first.

Interventions

  • DEVICE Breath synchronized abdominal FES
  • DEVICE Sham breath synchronized abdominal FES

Trial Details

FieldValue
Enrollment Target 250 participants
Start Date 2024-02-15
Est. Completion 2026-05-01
Phase NA
Liberate Medical

3 total trials

What the finished NCT05759013 record still lists

NCT05759013 is an interventional study that assigns participants to a tested intervention. The registered 250 participants enrollment target is mid-sized for trials with a published cap, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (82% lower).

The record links to 0 conditions, and to 2 interventions - of which Breath synchronized abdominal FES is the first listed.

NCT05759013 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT05759013 about?

NCT05759013 is a clinical study titled "Pivotal Evaluation of Abdominal Neuromuscular Electrical Stimulation (VentFree) for Weaning From Mechanical Ventilation". The objective of this study is to evaluate the efficacy of the VentFree Respiratory Muscle Stimulator (VentFree) in critically ill adult patients who require invasive mechanical ventilation, when compared to sham.

What is the current status of trial NCT05759013?

This trial is currently completed. It is a NA study. The enrollment target is 250 participants. The study started on 2024-02-15. Estimated completion is 2026-05-01.

What interventions are being tested in trial NCT05759013?

The interventions under investigation include: Breath synchronized abdominal FES (DEVICE), Sham breath synchronized abdominal FES (DEVICE).

Who is sponsoring clinical trial NCT05759013?

This trial is sponsored by Liberate Medical, which has 3 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT05759013's enrollment target sits among peer trials

250 410th of 2000 higher than 1,567 of 2,000 other NA trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT05759013, the US trial registry maintained by the National Library of Medicine. NCT05759013 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.