Haloperidol for Delirium in Adult Critically Ill Patients

Critical Illness Clinical Trial

— EuRIDICE  

Official title:

Efficacy of Haloperidol to Decrease the Burden of Delirium in Adult Critically Ill Patients (EuRIDICE): a Prospective Randomised Multi-center Double-blind Placebo-controlled Clinical Trial

Clinical Trial Details — Status: Terminated

Administrative data

• NCT number: NCT03628391
• Other study ID #: MEC-2017-115/NL62689.078.17
• Status: Terminated
• Phase: Phase 3
• Start date: February 22, 2018
• Est. completion date: January 23, 2021

Study information

• Verified date: May 2022
• Source: Erasmus Medical Center
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The EuRIDICE trial will study whether haloperidol as a first line treatment for ICU delirium reduces delirium duration (and severity). Adverse outcomes typically associated with delirium will also be studied and include long term cognition, functional outcome and quality of life. Further, patient and family experiences and cost-effectiveness will be assessed. Finally, safety concerns associated with the use of haloperidol in this vulnerable population will be studied.

Description:

BACKGROUND. Although widely used, the efficacy and safety of haloperidol for delirium in critically ill adults remain unclear. A randomised controlled trial is warranted to study the effect of haloperidol on delirium or coma, long-term outcomes, safety concerns, and cost-effectiveness. SUMMARY. The investigators will perform a multi-center, randomised, double-blind, placebo-controlled clinical trial to evaluate the use of haloperidol for delirium treatment in 742 critically ill adults with delirium. Days spent without delirium- or coma in the first 14 days after randomisation is the primary outcome. Study drug will be initiated at 2.5mg IV q8h and increased after 24 hours to 5mg IV q8h if delirium persists. Study drug dose will be tapered when delirium has resolved during 24 hours. All patients will be managed with a standardized pain, agitation and delirium protocol. Standard operating procedures for agitation (analgesia titration, alpha2 agonists) and hallucination management (atypical antipsychotics) will be implemented to accommodate possible imbalances of these symptoms in both treatment arms. Open-label haloperidol administration is discouraged during the trial. The sample size provides a power of 90% to detect statistically significant results (p<.05) and a true treatment difference of one day for the primary outcome between trial arms. This trial is expected to answer the clinically relevant question whether haloperidol still deserves a place in ICU delirium management. The primary outcome (delirium- and coma-free days) will be related to the secondary outcomes cognitive dysfunction, functional and psychological outcomes and patient- and family experiences. An extensive cost-effectiveness analysis will be done. Mortality at one year and safety concerns of haloperidol (QTc prolongation on EKG and rigidity) will be assessed as secondary endpoints. In conclusion, this large multicentre trial will assess efficacy and safety of haloperidol for ICU delirium.

Recruitment information / eligibility

• Status: Terminated
• Enrollment: 142
• Est. completion date: January 23, 2021
• Est. primary completion date: February 3, 2020
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria for randomisation:

1. Delirium, as assessed with the Intensive Care Delirium Screening Checklist - ICDSC: =4 or Confusion Assessment Method for the ICU - CAM-ICU: positive). NB Delirium can occur in the course of ICU admission or be present at admission.

2. Written Informed Consent is obtained from patient or legal representative

3. Complies with inclusion criteria but NOT exclusion criteria for eligibility:

Eligibility Inclusion criteria for eligibility

1. Age = 18 years

2. Admitted to ICU. Exclusion criteria for eligibility

1. Admitted to ICU with a neurological diagnosis (such as acute stroke, traumatic brain injury, intracranial malignancy, anoxic coma). Previous non-acute stroke or other previous neurological condition without cognitive deterioration is not an exclusion criterion.

2. Pregnancy (to be excluded by pregnancy test in women of child baring age)

3. History of ventricular arrhythmia including "torsade de pointes" (TdP)

4. Known allergy to haloperidol

5. History of dementia or an Informant Questionnaire on Cognitive Decline in the Elderly (IQCODE) score = 4

6. History of malignant neuroleptic syndrome or parkinsonism (either Parkinson's disease or another hypokinetic rigid syndrome)

7. Schizophrenia or other psychotic disorder

8. Inability to conduct valid delirium screening assessment (e.g. coma, deaf, blind) or inability to speak Dutch

9. The patient is expected to die within 24 hours, or is expected to leave the ICU within 24 hours after evaluation (may be reassessed daily)

Exclusion Criteria for randomisation:

1. Prolonged QT-interval (QTc > 500ms)

2. (recent) "torsade de pointes" (TdP)

3. (recent) malignant neuroleptic syndrome or parkinsonism

4. Evidence of acute alcohol (or substance) withdrawal requiring pharmacological intervention (e.g. benzodiazepines or alfa-2 agonist) to treat

5. IQCODE not assessed

6. The patient is expected to die within 24 hours, or is expected to leave the ICU within 24 hours.

7. No (previously) signed informed consent by patient or representative

8. Current participation in another intervention trial that is evaluating a medication, device or behavioural intervention

Related Conditions & MeSH terms

• Cognitive Decline
• Cognitive Dysfunction
• Cognitive Impairment
• Critical Illness
• Delirium
• Intensive Care Psychosis

Intervention

Drug:
• Haloperidol
haloperidol for ICU delirium, titrated on validated screening tool-based diagnosis
• Placebo
placebo for ICU delirium, titrated on validated screening tool-based diagnosis

Locations

Country	Name	City	State
Netherlands	Jeroen Bosch ziekenhuis	's-Hertogenbosch
Netherlands	IJsselland Hospital	Capelle aan den IJssel
Netherlands	Albert Schweitzer Hospital	Dordrecht
Netherlands	Radboudumc	Nijmegen
Netherlands	ErasmusMC	Rotterdam
Netherlands	Franciscus Gasthuis (Hospital)	Rotterdam
Netherlands	Ikazia Hospital	Rotterdam
Netherlands	Maasstad Hospital	Rotterdam

Sponsors (2)

Lead Sponsor	Collaborator
Erasmus Medical Center	ZonMw: The Netherlands Organisation for Health Research and Development

Country where clinical trial is conducted

Netherlands, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	delirium- and coma-free days	days without brain dysfunction (=delirium OR coma) while at the ICU	within the first 14 days after randomisation
Secondary	Cognitive deterioration: Global cognitive functioning	Global cognitive functioning as assessed with the Montreal Cognitive Assessment (MOCA). Total score will be reported, with a range of 0-30 (higher values representing better cognitive functioning).	3 and 12 months
Secondary	Cognitive deterioration: Verbal learning and memory	Auditory-verbal learning and memory will be assessed with the Rey Auditory Verbal Learning Test. Three subscores will be reported: total correct words in 5 trials (range: 0 -75), total correct words after delay (range: 0-15) and total correct words at recognition (range: 0-30).	3 and 12 months
Secondary	Cognitive deterioration: Semantic fluency	Semantic fluency will be tested with the Semantic Category Fluency Test. The amount of animals given within a time of 60 seconds will represent the score.	3 and 12 months
Secondary	Cognitive deterioration: Working memory	Working memory will be assessed using the Wechsler Adult Intelligence Scale - Third Edition (WAIS-III). Subscales will be reported for both digit span under forward and backward recall conditions. In addition, a total score will be reported, which equals the sum of both separate digit spans.	3 and 12 months
Secondary	Cognitive deterioration: Cognitive flexibility	Cognitive flexibility, one of the executive funcions, will be assessed with the Trialmaking tests A and B. The total amount of seconds needed to finish each test will be reported, with less seconds needed representing better cognitive flexibility.	3 and 12 months
Secondary	Cognitive deterioration: Word retrieval	Word retrieval is tested with the Boston Naming Test (30-item version). The total score (range: 0-30) represents the amount of correct answered drawings.	3 and 12 months
Secondary	Anxiety and depression	Anxiety and depression will be assessed with the Hospital Anxiety and Depression Scale (HADS). Two subscales will be reported, one for anxiety symptoms (range: 0-21) and one for depression symptoms (range: 0-21). Higher values represent a worse outcome. A subscore >8 indicates anxiety or depression, respectively.	3 and 12 months
Secondary	Functional outcome	Health-related quality of life will be assessed with the Short Form-35 (SF-36). Nine subscales will be reported on a 0 - 100 scale: physical functioning, role functioning - physical, bodily pain, general health, vitality, social functioning, role functioning - emotional, mental health and reported health transition. Higher values represent a better health-related quality of life.	3 and 12 months
Secondary	mortality	mortality	28 days and 1 year
Secondary	length of stay at ICU	length of stay at ICU (days)	days of ICU stay (time in days from ICU admission until ICU discharge). Assessed up to a maximum of 12 months after randomisation (end of follow-up period).
Secondary	Adverse drug associated events: prolonged QTc by EKG	prolonged QTc by EKG (ms)	while on study drug treatment during study period at ICU (up to 14 days after randomisation)
Secondary	Adverse drug associated events: muscle rigidity and other associated movements disorders	muscle rigidity and other associated movements disorders [measured with the Simpson Angus Scale]	while on study drug treatment during study period at ICU (up to 14 days after randomisation)
Secondary	Adverse drug associated events: ventricular arrhythmia's	ventricular arrhythmia's including torsade de pointes	during study period at ICU (up to 14 days after randomisation)
Secondary	Patients' memories related to their ICU stay	Patients' memories for their ICU stay will be evaluated with the ICU Memory Tool (ICU-MT). Subscores will be reported for factual memories (range: 0-11), delusion memories (range: 0-6) and memories of feelings (range: 0-4).	at discharge from hospital (up to a maximum of 12 months after randomisation = end of follow-up period) and 3 months after randomisation
Secondary	Patients' and family-members' experiences related to delirium	Delirium recall and distress related to the delirium episode will be assessed with the Delirium Experience Questionnaire (DEQ). Scores will represent whether patients remember their delirium episode. In addition, a score representing delirium-related distress levels (range: 0-4, with higher values representing more distress) will be reported for both patients and family-members.	at discharge from hospital (up to a maximum of 12 months after randomisation = end of follow-up period) and 3 months after randomisation
Secondary	Caregiver Strain	The strain experienced by family-members or relatives will be assessed with the Caregiver Strain Index. A total score (range: 0-13) will be reported, with higher values representing higher experienced strain.	at 3 months after randomisation
Secondary	Posttraumatic stress syndrome	Posttraumatic stress symptoms in patients and families will be assessed with the Impact of Event Scale - Revised (IES-R). A mean total IES-R score will be reported (range: 0-4), with posttraumatic stress disorder defined as a mean IES-R score = 1.6. In addition, subscores will be reported for intrusion, avoidance and hyperarousal (range: 0-4).	at 3 months after randomisation

External Links

•   Study website