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Clinical Trial Summary

FabLife is an interventional, prospective, multicentre, controlled study undertaken in metropolitan France.

The main objective is to evaluate the effect of FabLife personalised program over a period of 15 weeks on the improvement of spermatic DNA fragmentation in subfertile men compared to general dietary recommendations.


Clinical Trial Description

More than 15 % of couples couldn't get pregnant after at least a year of unprotected intercourse.

The FabLife personalised program aims to improve sperm quality including sperm DNA fragmentation in subfertile men through:

- A personalized dietary program based on patient's phenotype and genotype

- A daily dietary supplement, developed in the context of male infertility

A total of 75 patients will be recruited:

- 46 patients will benefit from the program,

- 23 patients will form the control group.

- 6 patients will not answer to all the criteria. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03475199
Study type Interventional
Source FabLife
Contact Eric M Lameignere, PhD
Phone + 33 784 29 59 71
Email e.lameignere@fablife.com
Status Recruiting
Phase N/A
Start date February 13, 2018
Completion date December 2019

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