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Comparison of Physiological Variables During Blood Donation

University of Colorado Denver (CU Denver) logo

University of Colorado Denver (CU Denver)

Status

Completed

Conditions

Hemorrhage

Study type

Observational

Funder types

Other
Industry

Identifiers

NCT02029807
13-2334

Details and patient eligibility

About

The investigators have developed a system based on a pulse oximeter, a tablet, and an algorithm running on the tablet that analyzes the pulse oximeter waveform.

The algorithm that runs on this system should be able to accurately keep track of blood loss during blood donation. The investigators will compare the algorithm with the blood loss tracked by a device called a flow meter.

The algorithm that runs on this system should be able to accurately keep track of stroke volume changes. The investigators will compare the algorithm with the stroke volume changes tracked by a device called a CCNexfin.

The algorithm that runs on this system should work whether it's in place for the whole blood donation, or if it's placed after the blood donation has started. The investigators will use two pulse oximeters for the system on each hand and compare one that is used for the whole blood donation versus one that is not used for the whole blood donation.

Full description

Hypothesis: p-values for testing the hypothesis of no correlation against the alternative that there is a nonzero correlation for each subject will be calculated. The minimum average power correlation, alpha = 0.05, will be used. Correlation will be made (CRI trend during 550ml blood volume removal) using pre and post blood draw data.

Specific Aims: These data will be submitted to the FDA with the following claims: The CRI algorithm

  1. Is intended for use by clinicians and medically qualified personnel to noninvasively display the trend of intravascular volume changes (hemorrhage)
  2. Is intended for use by clinicians and medically qualified personnel to noninvasively display the trend of stroke volume changes and
  3. The CRI trend value is not relative to an initial CRI reading, instead it is an actual CRI trend value that does

Enrollment

50 patients

Sex

All

Ages

18 to 89 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Subject is planning on donating blood and is approved by Children's Hospital Colorado's Blood Donation Center
  • Age 18-89 years
  • Previously donated blood (lower likelihood of vasovagal response)

Exclusion criteria

  • Pregnant
  • Incarcerated
  • Limited access to or compromised monitoring sites for non-invasive finger sensors

Trial design

50 participants in 1 patient group

Blood donors
Description:
Healthy adult volunteers donating blood

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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