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Adenosine 2A Receptor Agonist
Regadenoson infusion for Lung Transplant
Phase 1
Waitlist Available
Research Sponsored by Christine Lau, MD
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 72 hours
Awards & highlights
Study Summary
This trial will assess the maximum safe dose and duration of regadenoson that can be given to people undergoing a lung transplant.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 72 hours
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~72 hours
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Patient tolerability of assigned dose and duration
Secondary outcome measures
Activation of iNKT cells
Clinical Pulmonary Graft Dysfunction (PGD) score
Inflammatory Cytokines in blood and bronchioalveolar lavage
Trial Design
1Treatment groups
Experimental Treatment
Group I: Regadenoson infusionExperimental Treatment1 Intervention
Dose escalation of Regadenoson infusion
Find a Location
Who is running the clinical trial?
National Heart, Lung, and Blood Institute (NHLBI)NIH
3,837 Previous Clinical Trials
47,851,573 Total Patients Enrolled
3 Trials studying Lung Transplant
167 Patients Enrolled for Lung Transplant
Christine Lau, MDLead Sponsor
Frequently Asked Questions
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