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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 weeks
Treatment ~ Varies
Follow Up ~72 hours
This trial's timeline: 3 weeks for screening, Varies for treatment, and 72 hours for reporting.

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

~3 spots leftby Apr 2025