Clinical Trials Directory

Trials / Recruiting

RecruitingNCT06742437

Efficacy and Safety of a New Sperm Capacitation Method

Efficacy and Safety of a New Sperm Capacitation Method: a Prospective in Vitro Study on Semen Samples

Status
Recruiting
Phase
Study type
Observational
Enrollment
300 (estimated)
Sponsor
Fecundis Lab SL · Academic / Other
Sex
Male
Age
18 Years – 60 Years
Healthy volunteers
Accepted

Summary

Prospective, multicenter research study with a split-sample design on semen samples, without intervention, to evaluate the efficacy and safety of HyperSperm, a new sperm capacitation method, in 300 semen samples with various characteristics and abnormalities, in an in vitro study over 12 months.

Conditions

Interventions

TypeNameDescription
DEVICEStandard sperm preparationSperm samples in the control group will undergo traditional processing
DEVICEHyperSpermSperm samples in the experimental group will undergo product-specific processing

Timeline

Start date
2025-01-14
Primary completion
2026-06-01
Completion
2026-06-01
First posted
2024-12-19
Last updated
2026-02-27

Locations

4 sites across 1 country: Spain

Source: ClinicalTrials.gov record NCT06742437. Inclusion in this directory is not an endorsement.