About this trial
Sepsis is a common and life-threatening condition caused by a dysregulated host immune response to infection. Given the prominent role of endothelial breakdown and dysfunction in sepsis, therefore, there is an urgent need to establish strategies to protect the endothelium and preserve microcirculatory function.
This study is a randomised clinical study investigating intravenous fluid therapy and oral imatinib therapy in healthy human volunteers exposed to intravenous lipopolysaccharide (LPS).
The objective of the study is to investigate the biological effects of fluid and imatinib therapy on LPS-induced microcirculatory dysfunction.
Eligibility criteria
Qualifiers
Healthy adult volunteers aged between 18 and 40 years of age
Informed consent to participate
Disqualifiers
Current participation in a clinical trial
Pregnant or breastfeeding
Current history of smoking
Alcohol intake > 21 units per week
Trial design
Treatments tested in this trial
- Imatinib
- Compound sodium lactate solution
Treatment groups
Locations
Sponsors and collaborators
Belfast Health and Social Care Trust
Lead sponsor
Medical Research Council
Collaborator
The Royal College of Anaesthetists
Collaborator