Deplin® P.L.U.S. Program (Progress Through Learning Understanding & Support)

Completed

Conditions studied: Major Depressive Disorder

In brief

This study will be an observational study in which patients who have been prescribed Deplin® are invited to participate in surveys regarding their experiences with Deplin®. The purpose of this study is to increase the understanding of the role of L-methylfolate among patients who are candidates for Deplin®, provide patients with personalized education and support, and contribute to the overall understanding of the needs and concerns of patients being treated for depression.

Key facts

Study ID

NCT01369030

Run by

Pamlab, Inc.

People needed

554

Starts

2010-11-01

Expected to finish

2012-04-01

Last updated by the study team

2014-06-03

Who can join

Age: 18 and older, up to 70. Sex: any. Healthy volunteers: accepted.

You may qualify if…

• New Deplin® Start
• Only for patients with depression who have been prescribed brand name Deplin® to help metabolic management of depression.
• Clinically depressed patients who have been prescribed Deplin® in combination with an antidepressant.
• At the start of antidepressant therapy
• As augmentation to antidepressant therapy

You may not qualify if…

• Patients who do not meet DSM IV criteria for major depression
• If participant indicates that he or she did not get a prescription for Deplin®, he/she will not be able to complete the survey(s).
• For follow-up surveys, if the participant indicates that he/she has not been taking Deplin®, he/she will not be able to complete the survey(s).

Where it is running

• Moses Cone Family Practice Center — Greensboro, North Carolina, United States
• Vanderbilt University School of Medicine — Nashville, Tennessee, United States

Full record on ClinicalTrials.gov

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