Viewing Study NCT00234195



Ignite Creation Date: 2024-05-05 @ 12:04 PM
Last Modification Date: 2024-10-26 @ 9:20 AM
Study NCT ID: NCT00234195
Status: COMPLETED
Last Update Posted: 2007-04-17
First Post: 2005-10-04

Brief Title: Wellbutrin XL Major Depressive Disorder and Breast Cancer
Sponsor: Thomas Jefferson University
Organization: Thomas Jefferson University

Study Overview

Official Title: A Pilot Study of the Efficacy and Tolerability of Bupropion Extended Release Wellbutrin XL for the Treatment of Major Depressive Disorder in Women With Breast Cancer
Status: COMPLETED
Status Verified Date: 2007-04
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: To evaluate the efficacy of bupropion extended release Wellbutrin XL in the treatment of Major Depressive Disorder in women with breast cancer
To evaluate the tolerability of bupropion extended-release Wellbutrin XL in these patients
Detailed Description: This is research study for women diagnosed with breast cancer and major depression Women with breast cancer who are depressed may report greater pain poorer quality of life and worse overall functioning than those without depression The study will determine whether or not bupropion extended release Wellbutrin XLTM is useful in lessening the symptoms of depression in women with breast cancer One reason for conducting this research with bupropion extended release Wellbutrin XLTM instead of another antidepressant is because bupropion has a lower likelihood of causing the side effects of weight gain sexual dysfunction and fatigue which may be important for women with breast cancer and may even have a beneficial effect on these symptoms

Bupropion extended release Wellbutrin XLis approved by the United States Food and Drug Administration FDA for the treatment of major depression

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None
Secondary IDs
Secondary ID Type Domain Link
29000-J08101 None None None