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COMPLETED NA

Evaluation of The MetaNeb® System to Reduce Postoperative Pulmonary Complications

NCT02627742 · View on ClinicalTrials.gov ↗

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.

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

Sponsor

Hill-Rom

3 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT02627742

The ClinicalTrials.gov registry entry for NCT02627742 describes a study currently listed as completed. It is categorized as NA, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 419 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Hill-Rom, which has 3 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

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. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT02627742 reports 3 study locations spanning 3 distinct geographic areas — top geographies include Massachusetts, North Carolina, Pennsylvania. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

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. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT02627742?

The interventions under investigation include: MetaNeb® System (DEVICE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT02627742?

This trial is sponsored by Hill-Rom, which has 3 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

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.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial