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Feasibility of Prophylactic Haldol to Prevent Delirium in Cancer Patients — PHDC  

Delirium Clinical Trial

Official title:
Feasibility of Prophylactic Haldol to Prevent Delirium in Cancer Patients

Clinical Trial Summary

This research study proposes to conduct an open label, feasibility study administering prophylactic oral haldol to patients undergoing a hematopoietic stem cell transplant (HSCT).

The study will address the following research aims: 1) To demonstrate the feasibility of enrolling HSCT patients in a prophylactic medication trial, 2) To determine the tolerability of oral haldol in HSCT patients and 2) To compare rates of delirium in HSCT patients who receive prophylactic haldol with an untreated historical control group.

Clinical Trial Description

This is an open label, safety & feasibility, clinical drug trial. We will use historical controls from previous research with bone marrow transplant patients and delirium incidence at University of Iowa Hospitals and Clinics (UIHC) to evaluate the efficacy of prophylactic Haldol in the prevention of delirium. This study will recruit adult cancer patients undergoing hematopoietic stem cell transplant (HSCT) at UIHC. ;

Study Design

Related Conditions & MeSH terms

  • Delirium
  • Stem Cell Transplant Complications
Clinical Trial Details
NCT number NCT03489551
Study type Interventional
Source University of Iowa
Contact
Status Completed
Phase Phase 4
Start date November 2011
Completion date October 2013
View Details
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