Prazosin for Agitation in Alzheimer's Disease

Completed · Phase 2 · Has a placebo group

Conditions studied: Alzheimer's Disease, Disruptive Behavior

In brief

The study evaluates the effects of Prazosin on agitation in adults with Alzheimer's disease. Two thirds of the participants will participate in the medication portion, while one third will participate in the placebo portion

Key facts

Study ID

NCT03710642

Run by

Alzheimer's Disease Cooperative Study (ADCS)

People needed

35

Starts

2018-10-23

Expected to finish

2022-01-05

Last updated by the study team

2023-02-06

Who can join

Age: any. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Participants must meet all of the following criteria be included in the study:
• Men and women with probable or possible AD by NINCDS-ADRDA criteria utilizing history; medical records review; physical and neurological exam; and laboratory tests (as applicable). Brain neuroimaging is not a requirement.
• Participants must either reside in an LTC that is associated with the study site or at home with full-time caregiving.
• Participants must have disruptive agitation significant enough to disrupt caregiving and, in the opinion of the Site Principal Investigator, to justify treatment. Disruptive agitation, defined as having any combination of the following target behaviors, must have occurred nearly daily during the previous week and at least intermittently for 4 weeks prior to screening:
• irritability,
• physically and/or verbally aggressive behavior,
• physical resistiveness to necessary care
• pressured motor activity (e.g., pressured pacing) These behaviors must be problematic in that they cause participant and caregiver distress and/or interfere with essential care or disrupt their living environment. Target behaviors may be any combination of the listed domains. Disruptive agitation must meet this threshold at Screening, documented on the Behavioral Inclusion Criteria Checklist.
• Psychotropic medication, if used, should be stable for at least 2 weeks prior to randomization.
• If taking cholinesterase inhibitor and/or memantine, must be on stable dose for 3 months prior t o randomization.
• During the week before randomization, the above-described behaviors of eligible participants must be rated as of at least moderate severity.

You may not qualify if…

• Participants meeting any of the following criteria must not be included in the study:
• History of schizophrenia, schizoaffective disorder, or bipolar disorder according to the criteria of the most current version of the Diagnostic and Statistical Manual of Mental Disorders (DSM).
• Other neurodegenerative diseases, including Parkinsons disease and Huntingtons disease, or cerebral tumor.
• Dementia other than probable or possible AD per NINCDS-ADRDA criteria, such as human immunodeficiency virus (HIV) dementia, Creutzfeldt-Jakob disease, frontotemporal dementia, multiple cerebral infarctions, or normal pressure hydrocephalus.
• Current treatment for seizure disorder (Note: anticonvulsants prescribed for disruptive agitation in the absence of seizure disorder will be allowed).
• Abnormal laboratory values with clinical significance in the opinion of the site Principal Investigator.
• Current unstable medical illness including delirium, worsening congestive heart failure, unstable angina, recent myocardial infarction (within the past 3 months), acute infectious disease, severe renal or hepatic failure, severe respiratory disease, metastatic cancer, or other conditions that, in the Site Principal Investigators opinion, could interfere with the analyses of safety and efficacy in this study.
• Bedbound; participants may be ambulatory or use a wheelchair.
• Absence of any comprehensible language.
• Participation in another clinical trial for an investigational agent and took at least one dose of study drug (unless unblinded on placebo) within 12 weeks prior to screening. (The end of a previous investigational trial is defined as the date of the last dose of an investigational agent).
• Preexisting recurrent hypotension (systolic BP <110).
• If a reading of <110 systolic is measured at screening,
• If the individual is taking antihypertensive medication: The Site PI should reassess the need for such medication and consider medication adjustments in consultation with the participants physician. One week following adjustment of antihypertensive(s), screening BP will be repeated for reassessment of eligibility. Further adjustment of antihypertensive medication regimen by the participants health care prescriber, may be indicated if systolic pressure remains <110. For inclusion, new systolic measurement following medication adjustment must be ≥110.
• If the individual is not taking antihypertensive medication: repeat at least 3 BP measures over the course of 7-14 days. For inclusion, all three follow-up systolic measurements must be ≥110.
• Any systolic reading <100 is exclusionary.
• Preexisting orthostatic hypotension (>20 mmHg drop in systolic BP following 2 minutes of standing posture [or sitting if unable to stand] and accompanied by dizziness, lightheadedness, or syncope).
• A 2-week washout is required prior to BL for the following exclusionary medications: prazosin or other alpha-1 blocker, sildenafil, vardenafil, tadalafil, and avanafil.
• Women of childbearing potential are not included in this study. Women of non-childbearing potential are defined as any of the following:
• have been postmenopausal (no menstrual cycle for past 24 months)
• do not have a uterus,
• have bilateral tubal ligation,
• have undergone bilateral salpingectomy, and/or bilateral oophorectomy
• The participant may not be an immediate family member of personnel directly affiliated with this study, the study site or funding agency. Immediate family is defined as a spouse, parent, child, or sibling, any of whom may be related by blood, adoption, or marriage.
• P articipants whom the Site Principal Investigator deems to be otherwise unsuitable for participation.

Where it is running

• Banner Sun Health Research Institute — Sun City, Arizona, United States
• University of Southern California — Los Angeles, California, United States
• University of California, San Diego (UCSD) — San Diego, California, United States
• Alta California Medical Group — Simi Valley, California, United States
• Stanford University — Stanford, California, United States
• University of Kentucky — Lexington, Kentucky, United States
• Northern Light/Acadia Hospital Eastern Maine Medical Center — Bangor, Maine, United States
• SUNY Upstate Medical University — Syracuse, New York, United States
• VAMC: James J Peters — The Bronx, New York, United States
• Oregon Health and Science University — Portland, Oregon, United States
• Roper St. Francis Hospital — Charleston, South Carolina, United States
• University of Texas, Health Science Center San Antonio — San Antonio, Texas, United States
• University of Washington — Seattle, Washington, United States
• University of Washington — Seattle, Washington, United States

Full record on ClinicalTrials.gov

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