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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 aggression

measures 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

Page last updated: November 03, 2008

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