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NCT07710989Not yet recruiting

LIFU Effects & Outcomes: Mechanisms Evaluating Striatal Systems Imaging (LEO MESSI)

Mechanisms of Low-intensity Focused Ultrasound Targeting Striatal Circuits Underlying Auditory Hallucinations in Schizophrenia

Source: ClinicalTrials.gov · Last updated 5 Aug 2026

Brief summary (registry, in English)

Individuals with schizophrenia often experience persistent auditory hallucinations despite treatment with antipsychotic medications. Research suggests that abnormal communication between the striatum and the auditory cortex contributes to hallucinations. This first-in-human, proof-of-concept Phase 1 study will evaluate the safety, feasibility, and preliminary effects of repeated-session low-intensity focused ultrasound (LIFU), a non-invasive neuromodulation technique targeting the striatum. The study will examine whether LIFU can safely modulate brain circuits involved in hallucinations, reduce abnormal communication between the striatum and auditory cortex, and improve auditory hallucination symptoms.

Status (registry)
Not yet recruiting
Study type
Interventional
Enrollment
12 (estimated)
First submitted
6 Jul 2026
Start date
1 Feb 2027
Primary completion date
1 Dec 2027
Lead sponsor
University of California, San Francisco
NCT number
NCT07710989

What you commit to

  • Study type: Interventional
  • Planned participants: 12
  • From 1 Feb 2027 to the primary completion date, 1 Dec 2027
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • Clinically significant neurological disorder or MRI incompatibility

Who the study is looking for

  • 18-64 years of age, inclusive of all gender identities
  • Current DSM-5 diagnosis of schizophrenia
  • Persistent clinically-significant auditory hallucinations
  • No contraindications for MRI, confirmed via standard safety screening procedures
  • No neurological disorder
  • Clinically stable (outpatient past 12 weeks; same dose medications in 4 weeks)
  • Females will be tested for pregnancy and pregnant women will be excluded.

Age in the registry: 18 years to 64 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
University of California San Francisco
Coordinator of this site? Confirm its status
San FranciscoUnited StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.