Last updated on February 2019

Evaluation of Personalised Support Program Effectiveness in Sperm Quality Improvement


Are you eligible to participate in this study?

You may be eligible for this study if you meet the following criteria:

  • Conditions: Male infertility
  • Age: Between 18 - 45 Years
  • Gender: Male

Inclusion Criteria:

  • All male volunteers aged 18 to 45 years belonging to a couple reporting an involuntary infertility greater than 12 months
  • Conventional spermatic parameters compatible with spontaneous pregnancy
  • Sperm Count> 5M / ml and
  • Progressive sperm mobility> 20%
  • Negative spermoculture
  • Fragmentation of sperm DNA> 20%
  • Patient able to understand dietary recommendations given in French, in writing and orally
  • Social insured patient receiving benefits from the French Social Security health branch
  • Patient with a mobile phone (iOS or Android) with internet access

Exclusion Criteria:

  • Patient diagnosed with severe oligospermia (<5 million spz / ejaculate)
  • Patient with BMI> 35 or <18.5
  • Patient with known and treated diabetes
  • Patient with known and treated lipid disorders
  • Patient with known and treated cardiovascular diseases
  • Patients with known and treated hypertension
  • Patients with known and treated dysthyroidism
  • Patients with known symptomatic varicocele
  • Patient with known inflammatory bowel diseases
  • Patient with renal failure diagnosed
  • Patient presenting a viral risk (HIV / Hepatitis B and C / ...) requiring support in a dedicated circuit
  • Patient unable to give informed consent
  • Minors and protected adults, vulnerable people
  • Patient participating in another clinical research study

Recruitment Status: Open


Brief Description Eligibility Contact Research Team


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