Guanfacine to Treat Borderline Personality Disorder
Information source: Bronx VA Medical Center
Information obtained from ClinicalTrials.gov on November 03, 2008 Link to the current ClinicalTrials.gov record.
Condition(s) targeted: Borderline Personality Disorder
Intervention: guanfacine (Tenex) (Drug)
Phase: N/A
Status: Recruiting
Sponsored by: Mount Sinai School of Medicine Official(s) and/or principal investigator(s): Antonia S. New, M.D., Principal Investigator, Affiliation: Mount Sinai School of Medicine
Overall contact: Emily Hart, Phone: (212) 241-4459, Email: mpgroup@mssm.edu
Summary
This study is designed to investigate whether guanfacine (Tenex) is an effective treatment
for borderline personality disorder (BPD), an illness often characterized by unstable mood
and impulsive aggression. Guanfacine stimulates activity in the front portion of the brain,
a region associated with attention and the control of behavior. We believe that guanfacine
may improve symptoms of BPD by improving attention and aiding regulation of behavior.
Clinical Details
Official title: Guanfacine in the Treatment of Borderline Personality Disorder
Study design: Treatment, Non-Randomized, Double-Blind, Placebo Control, Parallel Assignment, Efficacy Study
Primary outcome: measures of impulsive aggressionmeasures of affective disturbance measures of social and occupational functioning measures of overall clinical status
Detailed description:
This is an 8-week treatment study designed to test whether guanfacine is an effective
treatment for borderline personality disorder (BPD). Prior to taking the study medication,
subjects will have medical and psychiatric evaluations, complete self-report questionnaires,
do a functional MRI scan, and complete a set of cognitive tests. While taking the study
medication, participants will meet weekly with a study doctor and be administered interviews
and questionnaires. At the end of the 8-week trial, participants will be asked to repeat the
MRI scan and cognitive tests.
Eligibility
Minimum age: 18 Years.
Maximum age: 55 Years.
Gender(s): Both.
Criteria:
Inclusion Criteria: This study includes men and women between the ages of 18 and 55 who
meet criteria for borderline personality disorder with impulsive aggression.
Exclusion Criteria: Subjects must not currently be taking any psychiatric medications.
Subjects must not meet criteria for current substance dependence, current major depression,
bipolar disorder, or schizophrenia-spectrum disorders.
Locations and Contacts
Emily Hart, Phone: (212) 241-4459, Email: mpgroup@mssm.edu
Mount Sinai Hospital - Mood & Personality Research Group, New York, New York 10029, United States; Recruiting
Additional Information
Starting date: July 2006
Last updated: July 31, 2006
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