Efficacy and Safety of Risperidone and Trazodone Monotherapy and Combination Therapy in Critically Ill Patients With Delirium
Launched by ROCHESTER GENERAL HOSPITAL · Apr 16, 2014
Trial Information
Current as of June 08, 2025
Withdrawn
Keywords
ClinConnect Summary
Delirium is defined as a disturbance of consciousness characterized by an acute onset of impaired cognitive function. Although delirium is thought to be common in the Intensive Care Unit (ICU) there are few studies that have evaluated its incidences, risks and outcomes. It has been associated with increased morbidity, and mortality and increased cost to the healthcare system. In addition to the uncertainty of the incidence of ICU delirium, there is a lack of information about the effects that certain pharmacological treatments have on delirious patients.
The rationale for this study is to ...
Gender
ALL
Eligibility criteria
- Inclusion Criteria:
- • Age greater than 18 years old who are admitted for more than 24 hours in the MICU or SICU
- • Patients diagnosed with delirium by primary team (screened positive for delirium using the CAM-ICU or with clinical manifestations of delirium)
- • Patients have an order for as-needed haloperidol or have received a one-time dose of haloperidol within 24 hours of randomization
- • Patients must be tolerating enteral feeding (greater than 20 mL/hour for more than 12 hours)
- Exclusion Criteria:
- • Patients who are unlikely to survive 24 hours after admission to the ICU
- • Patients who are admitted with a primary neurological condition or injury (i.e. stroke, active seizures, prolonged coma, overdose)
- • Patients who can not actively participate in delirium assessment
- • Patients actively withdrawing from alcohol or narcotics
- • Patients who were treated with any antipsychotic or trazodone within 30 days prior to ICU admission
- • Patients with a marked baseline prolongation of the QTc interval (repeated demonstration of QTc interval greater 500 milliseconds (msec))
- • Patients with a history of Torsades de Pointes
- • Patients with current treatment with an agent having either the potential to affect or increase the risk of QTc prolongation (e.g. erythromycin, any class Ia, Ic, or III antiarrhythmics)
- • Patients being treated with a neuromuscular blocker
- • Patients in whom haloperidol, risperidone, or trazodone is contraindicated
- • Pregnant patients or patients who are breast-feeding
- • Patients with a modified Blessed dementia rating scale score ≥4 or an Informant Questionnaire of Cognitive Dysfunction in the Elderly Score ≥4
- • Patients in which informed consent can not be obtained from the legally authorized representative
About Rochester General Hospital
Rochester General Hospital (RGH) is a leading healthcare institution dedicated to advancing medical research and improving patient care through innovative clinical trials. As a prominent sponsor, RGH leverages its extensive resources and expertise to conduct pioneering studies across various therapeutic areas, fostering collaboration among multidisciplinary teams of clinicians and researchers. Committed to ethical practices and regulatory compliance, RGH aims to enhance treatment options and contribute to the scientific community, ultimately ensuring that patients benefit from the latest advancements in medical science.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Rochester, New York, United States
Patients applied
Trial Officials
Mindee S Hite, Pharm.D.
Principal Investigator
Rochester General Hospital
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported
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