Clinical Trials Directory

Trials / Completed

CompletedNCT00975117

Spermotrend in the Treatment of Male Infertility

Assessment of the Efficacy of Dietary Supplement Spermotrend in the Treatment of Male Infertility

Status
Completed
Phase
Phase 3
Study type
Interventional
Enrollment
86 (estimated)
Sponsor
Catalysis SL · Industry
Sex
Male
Age
19 Years – 60 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to determine whether the administration of the dietary supplement Spermotrend improves spermatogenesis parameters in subjects with male infertility unrelated to major testicular conditions. The duration of this double-blind placebo controlled phase 3 clinical trial will be 24 weeks. The estimated number of males with infertility to be recruited and randomized for the study is 86.

Conditions

Interventions

TypeNameDescription
DIETARY_SUPPLEMENTPlaceboOne Placebo tablet (Orally administered) twice a day, for 12 weeks.
DIETARY_SUPPLEMENTSpermotrendOne Spermotrend tablet (Orally administered) twice a day, for 12 weeks

Timeline

Start date
2009-09-01
Primary completion
2011-03-01
Completion
2011-03-01
First posted
2009-09-11
Last updated
2011-03-08

Locations

1 site across 1 country: Cuba

Source: ClinicalTrials.gov record NCT00975117. Inclusion in this directory is not an endorsement.