Multiple Myeloma Clinical Trial

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Study of Hypotensive Hematopoietic Malignancy Patients’ USCOM Readings

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Summary

The purpose of this study is to test how practical it is to use the Ultrasonic Cardiac Output Monitor (USCOM), an FDA-approved device, on oncology patients (specifically those with blood cancers). Additionally, the researchers will learn if the USCOM gives additional information about patients' conditions when their blood pressures drop and they are treated with intravenous fluids.

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Eligibility Criteria

Inclusion Criteria:

-≥ 18 years of age

English speaker
Diagnosis of blood dyscrasia, hematopoietic malignancy, or condition that may requires HSCT

Exclusion Criteria:

Obstruction of the suprasternal notch that prevents placing the USCOM probe in the correct location
Tracheostomy or endotracheal tube that prevents placing USCOM probe in the correct location
Inability to lie flat, on left or right side, or with the head of bed at a 30 degree angle for the USCOM exam (ex. due to respiratory distress or physiologic reasons)
Impairment by a psychiatric, cognitive, or physiologic disorder that limits ability to understand explanation of study and give consent

Study is for people with:

Multiple Myeloma

Estimated Enrollment:

69

Study ID:

NCT01755000

Recruitment Status:

Completed

Sponsor:

Washington University School of Medicine

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There is 1 Location for this study

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Washington University School of Medicine
St. Louis Missouri, 63110, United States

How clear is this clinincal trial information?

Study is for people with:

Multiple Myeloma

Estimated Enrollment:

69

Study ID:

NCT01755000

Recruitment Status:

Completed

Sponsor:


Washington University School of Medicine

How clear is this clinincal trial information?

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