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Clinical Trial Summary

This study is being conducted to determine the clinical response rate for the regimen of L-methionine, betaine and folate for unipolar depression.


Clinical Trial Description

The study is 6 weeks long, with 9 clinical visits. All visits will take place at our location in Massachusetts. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT00226356
Study type Interventional
Source Cambridge Health Alliance
Contact
Status Completed
Phase Phase 4
Start date December 2004
Completion date September 17, 2008

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