Ketanserin Effects on Peripheral Temperature and Lactate (KoPTaL)
Critical Illness
About this trial
This is an interventional treatment trial for Critical Illness
Eligibility Criteria
Inclusion Criteria:
- DeltaTemperature greater that 6.0 °C.
- Age 18 years or older
- Admitted to the ICU for any reason
- Signed informed consent from the patient or legal representative
Exclusion Criteria:
- Pregnancy
- No possibility to obtain informed consent
- QTc above 550 msec,
- Arrhythmias, including bradycardia defined as a heart rate below 50/min; 2nd and 3rd degree AV block; ventricular tachycardia
- Blood Potassium level < 3.5 mmol/l
- Blood Magnesium level <0.5 mmol/l
- Allergy for ketanserin
- DeltaT less than 6°C.
- Patients undergoing therapeutic hypothermia
- Patients admitted after cardiac arrest
- Patients admitted after cardiac surgery
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Experimental
Placebo Comparator
Ketanserin
Placebo
Ketanserin is a serotonin type 2-receptor blocker (5-HT2). In normal endothelium, the 5-HT1 effects (vasodilation) are the most prominent [Dabire 1990]. In endothelium that is damaged, which is the case in sepsis, the 5HT2 effects (vasoconstriction) surpass the 5-HT1 effects. Blocking the 5-HT2 receptor with ketanserin can attenuate this pathological vasoconstriction. In addition, ketanserin has favourable α1-adrenergic blocking properties in the endothelium (vasodilation) that may further reverse the pathological vasoconstriction. In these ways ketanserin can reduce vasoconstriction and can improve the microcirculation.
The placebo is a standard glucose 5% solution.