Clinical Trials Directory

Trials / Unknown

UnknownNCT00358969

Guanfacine to Treat Borderline Personality Disorder

Guanfacine in the Treatment of Borderline Personality Disorder

Status
Unknown
Phase
N/A
Study type
Interventional
Enrollment
Sponsor
Icahn School of Medicine at Mount Sinai · Academic / Other
Sex
All
Age
18 Years – 55 Years
Healthy volunteers
Not accepted

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.

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.

Conditions

Interventions

TypeNameDescription
DRUGguanfacine (Tenex)

Timeline

Start date
2006-07-01
First posted
2006-08-01
Last updated
2006-08-01

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT00358969. Inclusion in this directory is not an endorsement.