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Assessment of Skin Perfusion Pressure as an Indicator of Tissue Oxygenation in Cardiac Surgery Patients Undergoing Cardiopulmonary Bypass

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ClinicalTrials.gov Identifier: NCT02329392
Recruitment Status : Completed
First Posted : December 31, 2014
Last Update Posted : April 29, 2016
Sponsor:
Information provided by (Responsible Party):
Yonsei University

Brief Summary:
This study is aim to evaluate usefulness of the perioperative monitoring of skin perfusion pressure as an indicator of perpheral perfusion in patients undergoing on-pump cardiac surgery. Association of the intraoperative and postoperative 6hr skin perfusion pressure with perioperative serum lactate level is going to be assessed.

Condition or disease
Peripheral Circulation During On-pump Cardiac Surgery

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Study Type : Observational
Actual Enrollment : 72 participants
Observational Model: Cohort
Time Perspective: Prospective
Study Start Date : December 2014
Actual Primary Completion Date : December 2015
Actual Study Completion Date : December 2015

Resource links provided by the National Library of Medicine

MedlinePlus related topics: Heart Surgery

Group/Cohort
SPP
Patients undergoing cardiac surgery with perioperative monitoring of Skin Perfusion Pressure



Primary Outcome Measures :
  1. Assessment of skin perfusion pressure [ Time Frame: From post induction to 6 hours ]

Secondary Outcome Measures :
  1. Assessment of arterial lactate level [ Time Frame: From post induction to 48 hours ]


Information from the National Library of Medicine

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Ages Eligible for Study:   20 Years and older   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Sampling Method:   Probability Sample
Study Population
Patinets > 20 years old who are scheduled for elective on-pump cardiac surgery
Criteria

Inclusion Criteria:

  • age > 20 yrs, scheduled for elective on-pump cardiac surgery

Exclusion Criteria:

  • known peripheral arterial occlusive disease, patients without swan ganz catheter insertion, heart transplantation, infective endocarditis, emergency surgery, hemodynamic instability requiring vasopressor, preoperative lactate > 2mmol/L, known liver cirrhosis, pregnant, cognitive dysfunction, being unable to communicate

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT02329392


Locations
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Korea, Republic of
Severance Hospital
Seoul, Korea, Republic of, 03722
Sponsors and Collaborators
Yonsei University
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Responsible Party: Yonsei University
ClinicalTrials.gov Identifier: NCT02329392    
Other Study ID Numbers: 1-2014-0070
First Posted: December 31, 2014    Key Record Dates
Last Update Posted: April 29, 2016
Last Verified: April 2016