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
| Type | Name | Description |
|---|---|---|
| DRUG | guanfacine (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.