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Comparing Antipsychotic Medications in LBD Over Time
A Pragmatic Randomized Trial Comparing Antipsychotics in Lewy Body Disease
Who can join
All ages · All sexes
Full eligibility criteria
Inclusion Criteria: * Patients seen in the neurology clinic at UT Health San Antonio * Diagnosed with psychosis due to PD or DLB * Requiring initiation of an antipsychotic medication * Clinical equipoise between quetiapine and pimavanserin must exist * The prescribing provider must be comfortable prescribing and managing both quetiapine and pimavanserin Exclusion Criteria: * Medical contraindication to either medication * Caregiver unavailable to complete NPI-Q * Currently taking an antipsychotic medication * Prescribing provider unwilling to manage either medication
About the study
The primary objective of this study is to determine whether treatment with pimavanserin or quetiapine is associated with a greater improvement in psychosis when used in a routine clinical setting to treat hallucinations and/or delusions due to Parkinson's disease (PD) or dementia with Lewy bodies (DLB) - collectively referred to as Lewy body disease (LBD).
What is being tested
- Pimavanserin (drug)
- Quetiapine (drug)
Sponsor: The University of Texas Health Science Center at San Antonio · Participants: 94 · Started: Apr 22, 2022
Contact the study team
- Carolyn Paiz, BS · Phone: 210-450-8830
Official record on ClinicalTrials.gov — NCT05590637
Locations in the U.S.
| Texas | UT Health Science Center - San Antonio, San Antonio University Health System, San Antonio |
Conditions
From ClinicalTrials.gov, data retrieved Sep 29, 2026. Each study sets its own eligibility; the study team decides who can join.