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Clinical Trial Summary

Investigate the clinical subtypes and the biological markers to personalize the use n-3 PUFAs (EPA, DHA, and EPA/DHA) in MDD.


Clinical Trial Description

In this proposal, the investigators aim to explore the clinical subtypes and biological markers to personalize the use n-3 PUFAs (EPA, DHA, and EPA/DHA) in MDD. By stratifying the subjects with (versus without) remission and treatment response, the biological markers are expected to have important prediction effects in future clinical practice. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03871088
Study type Interventional
Source National Science Council, Taiwan
Contact
Status Completed
Phase N/A
Start date July 2015
Completion date December 2018

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