Ischemia/Reperfusion Injury Clinical Trial
Official title:
Effects of Sevoflurane in Subanesthetic Concentrations on the Forearm Perfusion, Leukocyte/Thrombocyte Activation, and Endothelial Function After Tourniquet-Induced Ischemia/Reperfusion Injury in the Forearm of Volunteers
Sevoflurane preconditioning and cardiovascular protection against ischemia/reperfusion
injury.
Study hypothesis: The volatile anesthetic sevoflurane at subanesthetic concentrations
achieves endothelial protection against ischemia/reperfusion injury and reduces inflammatory
markers in the circulation
Healthy volunteers are included in the study to investigate endothelial function and
platelet activation after preconditioning by sevoflurane in subanesthetic concentrations.
Forearm perfusion, endothelial function and leukocyte/thrombocyte activation after
tourniquet-induced ischemia/reperfusion injury of the forearm are measured using healthy
volunteers in a cross-over design.
;
Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Crossover Assignment, Masking: Open Label, Primary Purpose: Treatment
Status | Clinical Trial | Phase | |
---|---|---|---|
Terminated |
NCT00948194 -
Effect of Nitric Oxide (NO) on Ischemic/Reperfusion Injury During Extended Donor Criteria (EDC) Liver Transplantation
|
N/A |