A clinical trial to study the effects of Paternia in male patients with Infertility

INTERVENTION: Intervention1: Paternia tablets: One tablet twice daily Intervention2: Paternia tablets: Two tablets twice daily Control Intervention1: Placebo: Two tablets twice daily CONDITION: Male Infertility PRIMARY OUTCOME: Improvement in sperm count, motility, morphology, motility index, teratozoospermia index (TZI), Fertilization potential by HOS test‐‐‐‐‐‐Timepoint: Day 0, 90, 180, 270 & 360 SECONDARY OUTCOME: Pregnancy Rate‐‐‐‐‐‐Timepoint: Day 0, 30, 60, 90, 180, 270 & 360 INCLUSION CRITERIA: 1. Age between 21 to 50 years 2. Sperm count ? < 50 million/cu mm 3. Sperm motility < 50 % (according to World Health Organization [WHO] 1999 criteria) 4. Normal Sperm morphology < 50 % 5. No history of taking therapy for infertility 6. No history of obstructive azoospermia 7. Normal female partner 8. Willing to sign Informed consent 9. Subjects likely to be available for all visits during follow‐up period