Validation of Transcutaneous Monitoring of Carbon Dioxide During Cardiopulmonary Bypass

Overview

About this study

The purpose of this study is to gather information about non-invasive measurements of the blood using the SenTec Digital Monitoring System to see if they are equivalent to currently used measurements. The SenTec Digital Monitoring System takes measurements of the carbon dioxide in your blood.

Participation eligibility

Participant eligibility includes age, gender, type and stage of disease, and previous treatments or health concerns. Guidelines differ from study to study, and identify who can or cannot participate. There is no guarantee that every individual who qualifies and wants to participate in a trial will be enrolled. Contact the study team to discuss study eligibility and potential participation.

Inclusion Criteria:

Those cases in which adult (18 years or older) patients of greater than 110 lbs (50kg) are scheduled to undergo open cardiac procedures involving surgical correction of one or more cardiac valves or combined valve/coronary procedures

Exclusion Criteria:

Patient age less than 18 years
Pregnant females
Emergent cases

Participating Mayo Clinic locations

Study statuses change often. Please contact the study team for the most up-to-date information regarding possible participation.

Mayo Clinic Location	Status
Rochester, Minn. Mayo Clinic principal investigator Matthew Schuldes, C.C.P.	Closed for enrollment

Mayo Clinic Location

Status

Rochester, Minn.

Mayo Clinic principal investigator

Matthew Schuldes, C.C.P.

Closed for enrollment

More information

Publications

Publications are currently not available

Clinical Trials