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NCT03783884 · ClinicalTrials.gov registry record · NA

A Protocol Comparing Temporary Transvenous Diaphragm Pacing to Standard of Care for Weaning From Mechanical Ventilation

A NA study, sponsored by Lungpacer Medical.

Terminated
Registry status
NA
Development phase
223
Enrollment target

NCT03783884: Clinical Trial NA study, sponsored by Lungpacer Medical.

NCT03783884 is a NA study that was terminated before completion, run by Lungpacer Medical. The registered enrollment target is 223 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (84% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT03783884, a NA study, was terminated before completion, sponsored by Lungpacer Medical.

TERMINATED
Registry status
NA
Development phase
223 participants
Enrollment target

Study Summary

This clinical investigation is an open-label, multi-center RCT to demonstrate the safety and effective performance of the Lungpacer DPTS (plus standard of care) as compared to Control (standard of care only) in patients aged 18 years or older who are receiving mechanical ventilation. Eligible Subjects will have received mechanical ventilation for ≥96 hours (4 days) and have failed two weaning attempts. The goal or outcome is to show a numerically greater proportion of subjects weaned in the Treatment (Lungpacer DPTS) group as compared to the Control group.

Primary Outcome

The proportion of subjects who are successfully weaned will be statistically significantly greater for subjects randomized to Treatment (Lungpacer DPTS) compared to subjects randomized to Control.

Interventions

  • DEVICE Lungpacer Diaphragm Pacing Therapy

Trial Details

FieldValue
Enrollment Target 223 participants
Start Date 2019-06-14
Est. Completion 2023-01-27
Phase NA
Lungpacer Medical

3 total trials

Why NCT03783884 stopped before completion

NCT03783884 is an interventional study that assigns participants to a tested intervention. The registered 223 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 (84% lower).

The record links to 0 conditions, and to 1 intervention - of which Lungpacer Diaphragm Pacing Therapy is the first listed.

NCT03783884 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT03783884 about?

NCT03783884 is a clinical study titled "A Protocol Comparing Temporary Transvenous Diaphragm Pacing to Standard of Care for Weaning From Mechanical Ventilation". This clinical investigation is an open-label, multi-center RCT to demonstrate the safety and effective performance of the Lungpacer DPTS (plus standard of care) as compared to Control (standard of care only) in patients aged 18 years or older who are receiving mechanical ventilation. Eligible Subjec...

What is the current status of trial NCT03783884?

This trial is currently terminated. It is a NA study. The enrollment target is 223 participants. The study started on 2019-06-14. Estimated completion is 2023-01-27.

What interventions are being tested in trial NCT03783884?

The interventions under investigation include: Lungpacer Diaphragm Pacing Therapy (DEVICE).

Who is sponsoring clinical trial NCT03783884?

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

How this trial's enrollment target compares

Where NCT03783884's enrollment target sits among peer trials

223 481st of 2000 higher than 1,520 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 NCT03783884, the US trial registry maintained by the National Library of Medicine. NCT03783884 (mid enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.