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Ketanserin Effects on Peripheral Temperature and Lactate (KoPTaL)

Primary Purpose

Critical Illness

Status
Unknown status
Phase
Phase 4
Locations
Study Type
Interventional
Intervention
Ketanserin
Placebo
Sponsored by
Onze Lieve Vrouwe Gasthuis
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Critical Illness

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

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

    Arm Type

    Experimental

    Placebo Comparator

    Arm Label

    Ketanserin

    Placebo

    Arm Description

    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.

    Outcomes

    Primary Outcome Measures

    Delta Temperature
    Delta Temperature is calculated from the difference between central (rectal) and peripheral (forefoot) temperature

    Secondary Outcome Measures

    Lactate clearance
    Lactate clearance is defined as :(Lactate (admission) - Lactate (8 hours))*100 / Lactate (admission) (Lactate (admission) - Lactate (8 hours))*100 / Lactate (admission) A lactate clearance of 10% or more is regarded as clinical relevant
    hospital length of stay
    Length of stay hospital
    mortality
    mortality at hospital discharge
    ICU length of stay
    length of stay in the ICU
    ICU mortality
    mortality at ICU discharge

    Full Information

    First Posted
    April 11, 2018
    Last Updated
    August 22, 2018
    Sponsor
    Onze Lieve Vrouwe Gasthuis
    Collaborators
    Medical Centre Leeuwarden
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    1. Study Identification

    Unique Protocol Identification Number
    NCT03646318
    Brief Title
    Ketanserin Effects on Peripheral Temperature and Lactate
    Acronym
    KoPTaL
    Official Title
    Ketanserin Effects on Peripheral Temperature and Lactate (KoPTaL)
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    August 2018
    Overall Recruitment Status
    Unknown status
    Study Start Date
    September 1, 2018 (Anticipated)
    Primary Completion Date
    April 1, 2019 (Anticipated)
    Study Completion Date
    May 1, 2019 (Anticipated)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Principal Investigator
    Name of the Sponsor
    Onze Lieve Vrouwe Gasthuis
    Collaborators
    Medical Centre Leeuwarden

    4. Oversight

    Studies a U.S. FDA-regulated Drug Product
    No
    Studies a U.S. FDA-regulated Device Product
    No
    Product Manufactured in and Exported from the U.S.
    No
    Data Monitoring Committee
    Yes

    5. Study Description

    Brief Summary
    A high blood lactate and a high peripheral to central temperature difference (deltaT) are associated with a higher mortality in critically ill patients. Both measures are signs of a reduced microcirculatory bloodflow or vasoconstriction and are associated with shock. It is unknown which medication can best be used to improve deltaT and lactate clearance. Ketanserin is being used in the intensive care setting for decades to optimize circulatory parameters. Ketanserin is a serotonin type 2-receptor blocker (5-HT2). Blocking the 5-HT2 receptor with ketanserin can attenuate pathological vasoconstriction. In these ways ketanserin can reduce vasoconstriction and can improve the microcirculation. As a consequence, the enhanced blood flow in the skin will increase the peripheral temperature and decrease deltaT. At the same time an increased flow in the microcirculation may lead to a reduction in lactate production. Objective: To determine the effects of a continuous ketanserin infusion on peripheral temperature and lactate clearance in critically ill patients with either a high lactate or a high deltaT.
    Detailed Description
    Rationale: A high blood lactate and a high peripheral to central temperature difference (deltaT) are associated with a higher mortality in critically ill patients. Both measures are signs of a reduced microcirculatory bloodflow or vasoconstriction and are associated with shock. On the other hand, it has not been shown yet that interventions leading to improvement of this temperature gap reduces mortality or improves any other outcome measurement. Moreover, it is unknown which medication can best be used to improve deltaT and lactate clearance. Ketanserin is being used in the intensive care setting for decades to optimize circulatory parameters. Ketanserin is a serotonin type 2-receptor blocker (5-HT2). Blocking the 5-HT2 receptor with ketanserin can attenuate pathological vasoconstriction. In these ways ketanserin can reduce vasoconstriction and can improve the microcirculation. As a consequence, the enhanced blood flow in the skin will increase the peripheral temperature and decrease deltaT. At the same time an increased flow in the microcirculation may lead to a reduction in lactate production. Objective: To determine the effects of a continuous ketanserin infusion on peripheral temperature and lactate clearance in critically ill patients with either a high lactate or a high deltaT. Study design: A multicentre double blind randomized controlled trial. Study population: All adult intensive care patients above 17 years old with a deltaT of >6°C with informed consent given by the patient or legal representative. Intervention (if applicable): The intervention is a continuous pump driven Ketanserin infusion of 0.75 ug/kg/min for eight hours. The control group will receive the same volume of glucose 5%. Main study parameters/endpoints: Change in DeltaT (measured per hour) Change in lactate (measured per 2 hours) Nature and extent of the burden and risks associated with participation, benefit and group relatedness: The risks of ketanserin infusion are limited but can be a QTc prolongation and a slight decrease in blood pressure. The study needs an arterial blood sample on inclusion, and after 2, 4, 6 and 8 hours of 1.5 ml each. In addition, a 6 ml blood sample at T=4 and T=8 hours.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Critical Illness

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Phase 4
    Interventional Study Model
    Parallel Assignment
    Model Description
    Randomised controlled trial (blinded)
    Masking
    ParticipantCare ProviderInvestigatorOutcomes Assessor
    Masking Description
    Placebo medication
    Allocation
    Randomized
    Enrollment
    120 (Anticipated)

    8. Arms, Groups, and Interventions

    Arm Title
    Ketanserin
    Arm Type
    Experimental
    Arm Description
    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.
    Arm Title
    Placebo
    Arm Type
    Placebo Comparator
    Arm Description
    The placebo is a standard glucose 5% solution.
    Intervention Type
    Drug
    Intervention Name(s)
    Ketanserin
    Intervention Description
    The dose of 0.75 ug/kg/min is a dose that has been used frequently in critically ill patients. The concentration of the study drug infusion will be 40 mg/40 ml glucose 5%. The maximum dose however will be 4.5 mg per hour for patients with a weight more than 100 kg. The pre-filled 50 ml syringes will be filled with 40 ml of a solution containing 40 mg ketanserin or 0 mg ketanserin in glucose 5%. The minimum number of ketanserin vials (2 ml with 5 mg/ml) that are needed is 240 (40 mg = 4 vials per patient). Duration of intervention: 8 hours
    Intervention Type
    Other
    Intervention Name(s)
    Placebo
    Intervention Description
    Glucose 5% solution
    Primary Outcome Measure Information:
    Title
    Delta Temperature
    Description
    Delta Temperature is calculated from the difference between central (rectal) and peripheral (forefoot) temperature
    Time Frame
    8 hours (after start of the study medication)
    Secondary Outcome Measure Information:
    Title
    Lactate clearance
    Description
    Lactate clearance is defined as :(Lactate (admission) - Lactate (8 hours))*100 / Lactate (admission) (Lactate (admission) - Lactate (8 hours))*100 / Lactate (admission) A lactate clearance of 10% or more is regarded as clinical relevant
    Time Frame
    8 hours (after start of the study medication
    Title
    hospital length of stay
    Description
    Length of stay hospital
    Time Frame
    6 months after start of study medication
    Title
    mortality
    Description
    mortality at hospital discharge
    Time Frame
    6 months after start of study medication
    Title
    ICU length of stay
    Description
    length of stay in the ICU
    Time Frame
    6 months after start of study medication
    Title
    ICU mortality
    Description
    mortality at ICU discharge
    Time Frame
    6 months after start of study medication

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    18 Years
    Accepts Healthy Volunteers
    No
    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

    12. IPD Sharing Statement

    Plan to Share IPD
    No

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    Ketanserin Effects on Peripheral Temperature and Lactate

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