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Search / Trial NCT02118688

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Withdrawn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.

Locations

Rochester, New York, United States

Patients applied

0 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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