Pharmacokinetics and Clinical Effects of Escalating Doses of Clonidine in ICU Patients (Clokin1)

Deventer Ziekenhuis

Status and phase: Completed; Phase 3

Conditions: Delirium; Critical Illness

Treatments: Drug: Clonidine (Catapresan®) 0,150 mg/ml, ampoule 1 ml

Study type: Interventional

Funder types: Other

Identifiers

NCT02466373

Clonidine kinetics 1.1

Details and patient eligibility

About

This study is developed for assessing the pharmacodynamic and pharmacokinetic properties of intravenous (IV) clonidine in critically ill patients on the ICU, and to estimate the optimal dosing strategy for IV clonidine.

Full description

Many patients in intensive care units (ICU's) require sedation and analgesia to tolerate mechanical ventilation and other ICU procedures. Commonly used GABA-ergic anaesthetics like propofol, midazolam and morphine have potential adverse effects that may increase morbidity, prolong ICU stay and provoke delirium. Recent studies have shown that sedation with alpha-2-adrenergic agonists may lead to a reduction of the total amount of gamma-aminobutyric acid (GABA) -ergic anaesthetics and reduction of delirium1In clinical practice the alpha-2-adrenergic agent clonidine is widely used off label as an add-on sedative in mechanically ventilated patients who suffer from delirium, but there are no large studies proving that this therapy is effective and safe. Limited information exists on the pharmacokinetics of iv clonidine, especially in ICU patients. Besides, dosing regimens of clonidine differ widely among ICU's in the Netherlands, and in the literature.

The sample size required for pharmacokinetic modelling with an acceptable level of precision is inversely related to the number of blood samplings taken from each individual. Population pharmacokinetic experiments that have been published have generally used 50 or more subjects. However, in the investigators study a relatively large number of blood samples are taken (>10 per subject when the protocol is completed, see section 6.3). THe investigators estimate that sufficient precision can be obtained with a sample size of 24 subjects, generating an estimated 240 to 360 blood samples.

In a recent publication of a computer simulated population pharmacokinetics of an absorption model using a design that involved 6 samplings per subject, it was estimated that a two-compartment first-order model would need 50 subjects (i.e. 300 blood samplings) to obtain a model with 50% precision and a power of 0.8.

The investigators 24 subjects will be treated with 3 different doses of clonidine (600, 1200 and 1800 µg/day), that is 8 per treatment arm.

On top of this, 8 patients receiving no clonidine will serve as a reference group, in order to interpret hemodynamic and safety data, and to illustrate dose-response relationships.

Enrollment: 32 patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

In order to be eligible to participate in this study, a subject must be:

• at least 18 years of age
• intubated
• sedated at the start of the study. Because of the high incidence of delirium on the ICU in all age categories, all age groups > 18 years will be included

Exclusion criteria

• Severe neurotrauma,
• Severe dementia (living in a nursing home)
• Inability to speak Dutch or English, which is one of the causes of not being able to use the CAM-ICU.
• The use of clonidine during the 96 hours before the start of the study.
• Bradycardia (<50/min)
• Severe hypotension (MAP < 65 after volume resuscitation and vasopressors)
• Pregnancy and lactation (pregnancy test are routinely performed in premenopausal women on the ICU).
• Epilepsy
• Known clonidine intolerance
• Liver cirrhosis (Child Pugh class C)
• Recent and acute myocardial infarction
• Severe heart failure (LVEF < 30%)
• Second or third degree atrioventricular (AV)-block without a permanent pacemaker
• Expected transfer to another hospital.

Trial design

Primary purpose: Treatment

Allocation: Non-Randomized

Interventional model: Parallel Assignment

Masking: None (Open label)

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32 participants in 4 patient groups

No clonidine

No Intervention group

Description:

No clonidine is administered. The outcome measures are recorded, to compare them with the outcome measures of the other clonidine arms

Clonidine 600mcg

Experimental group

Description:

4 patients receive 600 µg/day of clonidine without loading schedule. 4 patients receive 600 µg/day of clonidine with a loading schedule of 300 µg in 4 h.

Treatment:

Drug: Clonidine (Catapresan®) 0,150 mg/ml, ampoule 1 ml

Clonidine 1200mcg

Experimental group

Description:

* 4 patients receive 1200 µg/day of clonidine without loading schedule. * 4 patients receive 1200 µg/day of clonidine with a loading schedule of 600 µg in 4 h.

Treatment:

Drug: Clonidine (Catapresan®) 0,150 mg/ml, ampoule 1 ml

Clonidine 1800mcg

Experimental group

Description:

* 4 patients receive 1800 µg/day of clonidine without loading schedule. * 4 patients receive 1800 µg/day of clonidine with a loading schedule of 900 µg in 4 h.

Treatment:

Drug: Clonidine (Catapresan®) 0,150 mg/ml, ampoule 1 ml