NCT01900769

Brief Summary

Although blood volume is such an important parameter in everyday clinical medicine it cannot be measured easily. As a matter of fact, it is almost never measured but estimated or calculated based upon numbers derived from mostly healthy patients. The investigators do not even know whether someone's normal - i.e. before a surgery - blood volume is actually anywhere close to the generally accepted estimate or calculation. Tests exist in which a substance of known concentration is diluted in a person's blood volume and the resulting concentration is then measured, which allows the blood volume to be calculated. However, none of these tests can be completed at the bedside since they are not fast and require considerable set-up. This study turns the above approach upside-down: we will dilute the blood slightly with a known small volume of an intravenous fluid commonly used in many clinical settings and measure the concentra-tion of hemoglobin - the oxygen carrier contained in red blood cells - before and after adding the fluid. That allows for similar calculations without using neither specialized substances nor equipment. Hemoglobin is routinely measured in laboratories and is often a routine test before and during surg-eries and in intensive care units. Devices that can measure hemoglobin through the skin without actually drawing any blood are avail-able. If found comparable to laboratory determination of hemoglobin they could provide for a bedside and almost real-time assessment of blood volume, something that could be extremely valuable for de-cision making in critical areas of medicine and promoting goal directed therapies.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
20

participants targeted

Target at below P25 for not_applicable

Timeline
Completed

Started May 2013

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

May 1, 2013

Completed
2 months until next milestone

First Submitted

Initial submission to the registry

July 12, 2013

Completed
4 days until next milestone

First Posted

Study publicly available on registry

July 16, 2013

Completed
2 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

September 1, 2013

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

September 1, 2013

Completed
Last Updated

February 19, 2014

Status Verified

February 1, 2014

Enrollment Period

4 months

First QC Date

July 12, 2013

Last Update Submit

February 17, 2014

Conditions

Outcome Measures

Primary Outcomes (1)

  • matching BV by Hemoglobin dilution (lab)

    5 - 40 minutes

Secondary Outcomes (1)

  • matching BV by Hemoglobin dilution (SpHb)

    5 - 40 minutes

Study Arms (1)

Blood Volume Dilution

EXPERIMENTAL
Drug: Blood Volume Dilution

Interventions

Blood Volume Dilution

Eligibility Criteria

Age18 Years - 50 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64)

You may qualify if:

  • healthy adults of normal constitution (weight/height)

You may not qualify if:

  • any ongoing or recent infusions (\< 24h ago) of any fluid/substance
  • morbid obesity
  • heart disease
  • hypertension
  • coagulopathy (bleeding disorder)
  • therapy with anti- or procoagulants
  • transfusion of any blood product
  • therapy with diuretics
  • therapy with vasopressors
  • vasodilators or inotropes
  • acute or chronic infections
  • immunocompromised status
  • hemodynamically unstable
  • hemorrhage (bleeding)
  • recent surgery
  • +2 more criteria

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

University of Arizona Medical Center

Tucson, Arizona, 85724, United States

Location

Study Officials

  • Kai Schoenhage, MD

    University of Arizona

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NA
Masking
NONE
Purpose
DIAGNOSTIC
Intervention Model
SINGLE GROUP
Sponsor Type
OTHER
Responsible Party
SPONSOR INVESTIGATOR
PI Title
Assistant Professor, Anesthesiology Director of Perioperative Services, Director of Liver Transplant Anesthesia, Department of Anesthesiology

Study Record Dates

First Submitted

July 12, 2013

First Posted

July 16, 2013

Study Start

May 1, 2013

Primary Completion

September 1, 2013

Study Completion

September 1, 2013

Last Updated

February 19, 2014

Record last verified: 2014-02

Locations