Investigation of Novel and Established Therapies in a Human Intravenous Lipopolysaccharide Model of Sepsis

Trial statusNot yet recruiting
Trial phasePhase 1, Phase 2
Trial typeInterventional
Biological sexAll
Age18-40
SponsorBelfast Health and Social Care Trust

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

65 Participants
are divided into 4 treatment groups

Locations

This trial has no locations

Sponsors and collaborators

Belfast Health and Social Care Trust

Lead sponsor

Medical Research Council

Collaborator

The Royal College of Anaesthetists

Collaborator