Buspirone for the Treatment of Traumatic Brain Injury (TBI) Irritability and Aggression

Completed · Phase 4 · Has a placebo group

Conditions studied: Traumatic Brain Injury

In brief

The purpose of this study is to improve behavior control displayed by persons with traumatic brain injury by assessing effectiveness of treatments for post-TBI irritability and aggression.

Key facts

Study ID

NCT01821690

Run by

Indiana University

People needed

81

Starts

2013-05-15

Expected to finish

2025-09-26

Last updated by the study team

2026-02-24

Who can join

Age: 18 and older, up to 70. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Closed head injury (impaired brain function resulting from externally inflicted trauma without penetrating injury as defined below) at least 6 months prior to enrollment
• Irritability that is either new or worse than level of irritability before the traumatic brain injury, by report of observer or person with TBI
• Age at time of enrollment: 18 to 70 years
• Voluntary informed consent of patient and observer
• Subject and observer willing to comply with the protocol
• Observer-rated NPI Irritability Domain score 6 or greater to include only moderate-severe irritability
• Medically and neurologically stable during the month prior to enrollment.
• If taking antidepressant, anxiolytic, hypnotic, or stimulant medications, no change anticipated in these medications during the month prior to enrollment
• No change in therapies or medications planned during the 91-day participation
• No surgeries planned during the 91-day participation
• Vision, hearing, speech, motor function, and comprehension sufficient for compliance with all testing procedures and assessments
• Observer (e.g.: family member, close friend, employer) with whom subject interacts sufficiently to observe occurrences of irritability. The observer interacts with the participant for a period long enough and of a nature to be able to judge the participant's irritability. The interactions would need to be adequate to judge observer distress over the irritability, severity of irritability and frequency of irritability on the following scale: < once weekly; once per week; several times per week, but not every day; essentially continuous.

You may not qualify if…

• Potential subject without a reliable observer
• Penetrating head injury as defined by head injury due to gunshot, projectile or foreign object
• Injury < 6 months prior to enrollment
• Ingestion of buspirone during the month prior to enrollment
• Inability to interact sufficiently for communication with caregiver
• History of schizophrenia or psychosis
• Diagnosis of progressive or additional neurologic disease
• Clinical signs of active infection

Where it is running

• Indiana University and Rehabilitation Hospital of Indiana — Indianapolis, Indiana, United States

Full record on ClinicalTrials.gov

Trial information comes from ClinicalTrials.gov and is refreshed daily. TrialsForMe does not provide medical care and does not run the studies it lists.