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COMPLETED

Vibration Response Imaging (VRI) in Patients That Are Undergoing Pulmonary Interventional Procedure

NCT00672893 · View on ClinicalTrials.gov ↗

Study Summary

Vibration response imaging (VRI) technology, provides a radiation-free dynamic image of the lung, by visualizing vibration energy emitted during the respiration cycle (lung sounds). Airflow in the lungs during the respiration cycle creates vibrations that propagate through the lung tissue; these vibrations are affected by the structural properties of the lungs and may vary in space, time and frequency. Moreover, any structural alteration, such as a bronchial obstruction or space occupying infiltration, is reflected in a corresponding modification of the vibration response. As obstructions that occur in airways alter airflow, the VRI may provide additional lung function information prior to treatment for airway obstruction and during follow-up. Moreover, the VRI may provide the physician immediate evaluation of the improvement of air flow distribution, quantitative and qualitative measurements. Furthermore, the VRI is a non-invasive, radiation free procedure which is simple and doesn't require the level of patient effort required for lung function test and other evaluation.

Conditions Studied

Interventions

  • OTHER Vibration Response Imaging

Study Locations (5)

Other

  • Hospital St. Marguerite — Marseille
  • Thoraxklinik at Heidelberg University — Heidelberg

Colorado

  • National Jewish Medical and Research Center — Denver

North Carolina

  • Duke University Medical Center — Durham

Kanagawa

  • St. Marianna Hospital — Kawasaki

Trial Details

FieldValue
Enrollment Target 200 participants
Start Date 2006-02
Est. Completion 2008-12

Sponsor

Deep Breeze

2 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT00672893

The ClinicalTrials.gov registry entry for NCT00672893 describes a study currently listed as completed. It is categorized as an unspecified phase, 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 200 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Deep Breeze, which has 2 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 1 condition, with Central Airway Stenosis appearing as the primary indexed condition, and to 1 intervention — of which Vibration Response Imaging 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: NCT00672893 reports 5 study locations spanning 4 distinct geographic areas — top geographies include Other, Colorado, North Carolina. 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 NCT00672893 about?

NCT00672893 is a clinical study titled "Vibration Response Imaging (VRI) in Patients That Are Undergoing Pulmonary Interventional Procedure". Vibration response imaging (VRI) technology, provides a radiation-free dynamic image of the lung, by visualizing vibration energy emitted during the respiration cycle (lung sounds). Airflow in the lungs during the respiration cycle creates vibrations that propagate through the lung tissue; these vib...

What is the current status of trial NCT00672893?

This trial is currently completed. The enrollment target is 200 participants. The study started on 2006-02. Estimated completion is 2008-12.

What conditions does trial NCT00672893 study?

This clinical trial studies the following conditions: Central Airway Stenosis. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT00672893?

The interventions under investigation include: Vibration Response Imaging (OTHER). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT00672893?

This trial is sponsored by Deep Breeze, which has 2 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT00672893 being conducted?

This trial has 5 study locations across Colorado, North Carolina, Kanagawa. 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