Comparison of Different Locations for Pulse Oximetry Probes in Cardiovascular (CV) Patients With Poor Peripheral Perfusion

Terminated

• Conditions: Congestive Heart Failure; Cardiomyopathy

• Registration Number: NCT01128036
• Lead Sponsor: Saint Luke's Health System

Brief Summary

The purpose of this study is to determine if the forehand location for sensor placement has less episodes of signal dropout than the finger sensor location. In addition, this study will evaluate two finger sensors, which utilize different technology to compare signal quality.

Detailed Description

A comparison study design will be used to evaluate the signal quality of pulse oximetry sensors placed in two locations: forehand and finger. Each subject will serve as their own control, with measurements of signal quality evaluated at 2 second intervals over a period of one hour. The measurements will be recorded simultaneously with a computer program and laptop computer. Finger and forehand sensors will be applied according to manufacturer's guidelines. An output connection will be made from each pulse oximeter computer unit to a password protected, laptop computer for data downloading. Data will be collected for a 1 hour period at 2 second increments and stored in the hard drive of the laptop. Following completion of data collection, the study sensors will be removed.

Study Timeline

• Study Start: 2010-05
• Study First Submitted: 2010-05-20
• Study First Submitted QC: 2010-05-20
• Study First Posted: 2010-05-21
• Primary Completion: 2011-05
• Study Completion: 2011-05
• Status Verified: 2011-08
• Last Update Submitted: 2011-08-08
• Last Update Posted: 2011-08-09

Recruitment & Eligibility

• Status: TERMINATED
• Sex: All
• Target Recruitment: 51

Inclusion Criteria

• CICU patients with a new diagnosis or history of CHF or cardiomyopathy
• Patients with a medical order for pulse oximetry monitoring
• Age greater than or equal to 18 years of age
• English speaking
• Signs of hypoperfusion

Exclusion Criteria

• CICU patients with an impediment to sensor application
• CICU patients with excessive facial edema
• CICU patients with mechanical ventilation
• CICU patients with intra-aortic balloon pump therapy
• CICU patients with intravenous vasopressor drug administration

Study & Design

• Study Type: OBSERVATIONAL
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Signal quality loss (dropout rate)	Every 2 seconds for one hour

Trial Locations

Locations (1)

Saint Luke's Hospital; 🇺🇸 Kansas City, Missouri, United States