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NCT02627742 · ClinicalTrials.gov registry record · NA

Evaluation of The MetaNeb® System to Reduce Postoperative Pulmonary Complications

A NA study of Atelectasis and Pulmonary Complications, sponsored by Hill-Rom.

Completed
Registry status
NA
Development phase
419
Enrollment target
3
Study locations

NCT02627742: Completed NA study of Atelectasis and Pulmonary Complications, sponsored by Hill-Rom.

NCT02627742 is a NA study of Atelectasis and Pulmonary Complications that has completed, run by Hill-Rom. The registered enrollment target is 419 participants, above the 97-participant average among 3 other Atelectasis trials with a reported enrollment target (332% higher). The trial reports 3 study locations across 3 states. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT02627742, a NA study of Atelectasis and Pulmonary Complications, has completed, sponsored by Hill-Rom.

COMPLETED
Registry status
NA
Development phase
419 participants
Enrollment target
3
Study locations

Study Summary

To determine if a therapy regimen including treatment with The MetaNeb® System had a positive impact on the rate of pulmonary complications related to atelectasis and/or secretion retention that occur in high risk post-operative patients. This is a non-randomized facility (or hospital) level pre-post intervention study.

Primary Outcome

One or more of the following that occurs within seven (7) days of the post-surgical admission will be considered a Significant Postoperative Pulmonary Complication (PPC) * Patient requires prolonged mechanical ventilation (\> 24 hours from post-surgical admission) * Patient requires prolonged respiratory support for \> 24 hours from post-surgical admission * Diagnosis of pneumonia within seven (7) days * Readmission to ICU for pulmonary complications within seven (7) days of post-surgical hospi

Interventions

  • DEVICE MetaNeb® System

Study Locations (3)

Massachusetts

  • Lahey Hospital and Medical Center - Burlington

North Carolina

  • Carolinas Medical Center - Charlotte

Pennsylvania

  • Hospital of the University of Pennsylvania - Philadelphia

Trial Details

FieldValue
Enrollment Target 419 participants
Start Date 2016-03
Est. Completion 2017-08
Phase NA
Hill-Rom

18 total trials

What the finished NCT02627742 record still lists

NCT02627742 is an interventional study that assigns participants to a tested intervention. The registered 419 participants enrollment target is mid-sized for trials with a published cap, above the 97-participant average among 3 other Atelectasis trials with a reported enrollment target (332% higher).

The record links to 2 conditions, with Atelectasis appearing as the primary indexed condition, and to 1 intervention - of which MetaNeb® System is the first listed.

NCT02627742 reports a single indexed study location in Massachusetts, North Carolina, Pennsylvania.

Frequently Asked Questions

What is clinical trial NCT02627742 about?

NCT02627742 is a clinical study titled "Evaluation of The MetaNeb® System to Reduce Postoperative Pulmonary Complications". To determine if a therapy regimen including treatment with The MetaNeb® System had a positive impact on the rate of pulmonary complications related to atelectasis and/or secretion retention that occur in high risk post-operative patients. This is a non-randomized facility (or hospital) level pre-pos...

What is the current status of trial NCT02627742?

This trial is currently completed. It is a NA study. The enrollment target is 419 participants. The study started on 2016-03. Estimated completion is 2017-08.

What conditions does trial NCT02627742 study?

This clinical trial studies the following conditions: Atelectasis, Pulmonary Complications.

What interventions are being tested in trial NCT02627742?

The interventions under investigation include: MetaNeb® System (DEVICE).

Who is sponsoring clinical trial NCT02627742?

This trial is sponsored by Hill-Rom, which has 18 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT02627742 being conducted?

This trial has 3 study locations across Massachusetts, North Carolina, Pennsylvania. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Source: ClinicalTrials.gov NCT02627742, the US trial registry maintained by the National Library of Medicine. NCT02627742 (mid enrollment · single site footprint · completed) retrieved and formatted by PlainTrial, see methodology.