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Clinical Trials/NCT00143858
NCT00143858
Completed
N/A

Assessment of the Clinical Utility of Non Invasive Peripheral Signal Averaged Pulse Volume

University of Medicine and Dentistry of New Jersey1 site in 1 country16 target enrollmentSeptember 2004

Overview

Phase
N/A
Intervention
Not specified
Conditions
Peripheral Vascular Response
Sponsor
University of Medicine and Dentistry of New Jersey
Enrollment
16
Locations
1
Status
Completed
Last Updated
16 years ago

Overview

Brief Summary

The purpose of this study is to determine the clinical usefulness of measuring the heart's pumping ability by measuring the Peripheral Pulse Volume (PPV).

Detailed Description

Peripheral Pulse Volume (PPV) is the change in the volume of a limb that occurs when blood passes through the limb. The limb also acts as an electrical conductor whose electrical impedence changes with limb geometry and volume. Each time the heart beats, the volume of the limb segment changes, and therefore its electrical impedence changes. A plethysmograph can be used to measure volume changes of a part of the body by producing a plethysmographic waveform. Selectively capturing a number of these plethysmographic wave forms with acceptable noise levels and averaging them using the EKG as a reference-timing signal generate a highly reproducible pulse volume signal. Signal averaged pulse volume measurement will be obtained non-invasively from the lower extremities of patient volunteers. A disposal non-occluding electrical monitoring strap will be applied to the calf of each patient. Changes in the calf's size/volume caused by changes in the patient's cardiac output and calf blood flow will result in electrical impedance changes. These changes will be recorded by an analog admittance plethysmograph attached to the lower extremity strap. The analog plethysmograph is coupled to a digital computer for signal enhancement and measurement.

Registry
clinicaltrials.gov
Start Date
September 2004
End Date
October 2007
Last Updated
16 years ago
Study Type
Observational
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Not specified

Study Sites (1)

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