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Establish ProLung Test Measurement Collection Protocol for Future Studies.

NCT04134520 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 500

Last updated 2022-10-25

No results posted yet for this study

Summary

The purpose of this Study is to identify and test different data collection methods to determine which approaches improve the ProLung Testing procedure. Once this Study is complete, the Sponsor plans to evaluate these improvements in future follow up Validation studies that will assess device accuracy using the new measurement collection methods.

Conditions

  • Cancer , Healthy

Interventions

DEVICE

ProLung System

Non-invasive bioconductance measurements

Sponsors & Collaborators

  • Fresh Medical Laboratories

    lead INDUSTRY

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2020-02-14
Primary Completion
2024-10-16
Completion
2024-10-16
FDA Device
Yes

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04134520 on ClinicalTrials.gov