drugset / Trial / NCT03072589
Study to Evaluate Adenosine 2A Receptor Agonist (Regadenoson) in Patients Undergoing Lung Transplantation
Phase 1
Unknown
21 enrolled
Christine Lau, MD
National Heart, Lung, and Blood Institute (NHLBI) · collab
SequentialOpen-labelTreatment
Summary
This study will evaluate the maximum safe dose and duration of regadenoson (Lexiscan) that can be given to people who are having a lung transplant. Regadenoson will be given as a continuous IV infusion. All participants in the study will receive a regadenoson infusion beginning in the operating room during the lung transplant procedure. Participants will be assigned a certain dose of regadenoson to be given over a 12 or 24 hour period.
Timeline
- Start
- 2017-11-30
- Primary completion
- 2021-08-01
- Completion
- 2022-08-01
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Regadenoson | Diagnostic / imaging agent | 1.44 ug/kg | Intravenous |
Indications
No indication recorded.