Safety Evaluation of the HyperSperm Sperm Preparation Procedure for In Vitro Fertilization
ConditionInfertility
Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age20-45
SponsorFecundis Lab SL
About this trial
Prospective, multicenter, randomized clinical study evaluating the safety of a novel sperm preparation method for in vitro fertilization (IVF), compared to standard sperm preparation procedures.
Eligibility criteria
Qualifiers
Couples undergoing in vitro fertilization (IVF) treatment.
Planned use of fresh sperm samples obtained by masturbation.
Age between 20 and 42 years.
Antral follicle count ≥ 4.
Disqualifiers
Active sexually transmitted infection (STI).
Use of donor sperm.
Medical conditions contraindicating pregnancy or the IVF procedure.
Uterine anomalies associated with distortion of the uterine cavity.
Trial design
Treatments tested in this trial
- Standard Sperm Preparation
- HyperSperm
Treatment groups
202 Participants
are divided into 2 treatment groupsSponsors and collaborators
Source ClinicalTrials.gov