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OpenTrials
Completed

NCT Number: NCT02888431

Correlation of Arterial and Venous Lactate and Base Deficit Values

The purpose of this study is to determine the correlation between pH, base deficit, and lactate values when comparing venous and arterial blood samples in the pediatric population.

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Key information

Conditions

Arterial Access Central Venous Catheter Peripheral Access

Sex eligibility

All sexes

Study type

Observational

Primary location

Nationwide Children's Hospital

Columbus, Ohio, 43205, United States

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Patients requiring arterial access and peripheral access. Additionally, patients with a central venous catheter would be included.

Exclusion criteria

  • Patients who not require arterial access.

Treatment and study plan

bedside point-of-care device

Device

A bedside point-of-care device is routinely used in the operating room to measure lactate, base deficit, and pH.

Primary outcomes

  1. lactate blood value

    Time frame: During surgery- approximately 15-20 minutes after induction in the operating room (OR)

    blood will be drawn from peripheral venous line, arterial line, and/or central venous line then the lactate value will be assessed by using a bedside point-of-care device, called i-stat.

  2. base deficit blood value

    Time frame: During surgery- approximately 15-20 minutes after induction in the operating room (OR)

    blood will be drawn from peripheral venous line, arterial line, and/or central venous line then the base deficit blood value will be assessed by using a bedside point-of-care device, called i-stat.

  3. pH blood value

    Time frame: During surgery- approximately 15-20 minutes after induction in the operating room (OR)

    blood will be drawn from peripheral venous line, arterial line, and/or central venous line then pH blood value will be assessed by using a bedside point-of-care device, called i-stat.

Sponsors and collaborators

Lead sponsor

Joseph D. Tobias

Other

Registry information

Important dates

Study start
2015
Primary completion
2016
Study completion
2016
First posted
Sep 5, 2016
Registry last updated
Jan 31, 2017

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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