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Organ Preservation Device
Kidney perfusion pump for Kidney Transplant (SNOPO Trial)
N/A
Waitlist Available
Led By Patrick Luke, MD
Research Sponsored by Lawson Health Research Institute
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Adult male or females, 18 years or older
Active on the kidney transplant waiting list
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 1 year from start of study
Awards & highlights
SNOPO Trial Summary
This study is evaluating whether a new method of storing donor kidneys can improve outcomes after transplantation.
SNOPO Trial Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowSNOPO Trial Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 1 year from start of study
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~1 year from start of study
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Eligible versus actual kidney perfusions performed to assess study feasibility
Rate of kidney discard or graft failure attributed to the study intervention
Secondary outcome measures
Degree of ischemia-reperfusion injury by kidney biopsy
Post-transplant serum creatinine levels to assess graft function
Rate of delayed graft function in study participants
+1 moreSNOPO Trial Design
1Treatment groups
Experimental Treatment
Group I: Subnormothermic PerfusionExperimental Treatment1 Intervention
Kidneys retrieved for transplantation will undergo subnormothermic oxygenated perfusion using the study device and perfusion solution for at least 1 hour prior to transplantation into the recipient.
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Who is running the clinical trial?
Lawson Health Research InstituteLead Sponsor
655 Previous Clinical Trials
413,324 Total Patients Enrolled
Patrick Luke, MDPrincipal InvestigatorLawson Health Research Institute
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