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Non-Invasive Measurement of Respiratory Effort

NCT00528749 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 20

Last updated 2007-09-12

No results posted yet for this study

Summary

This study is intended to compare intrathoracic pressure and respiratory effort data obtained by forehead venous pressure and respiratory movement (FVP/RM) with data obtained by the current gold standard, esophageal manometry. If this feasibility study validates the ability of FVP/RM data to quantitatively measure respiratory effort non-invasively, further studies will be performed to validate the utility of the ARES device in diagnosis of the UARS.

Conditions

  • Upper Airway Resistance Syndrome

Interventions

OTHER

Patient will wear ARES device while undergoing sleep study

Device is worn on forehead

Sponsors & Collaborators

  • Advanced Brain Monitoring, Inc.

    collaborator INDUSTRY

  • Walter Reed Army Medical Center

    lead FED

Study Design

Allocation
NA
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2007-02-28

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 NCT00528749 on ClinicalTrials.gov