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The effect of red grape seed extract on human semen parameters

Evaluation of the effect of red grape seed extract on idiopathic infertile male patients’ spermogram at Royan infertility center in 2010

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
IRCT
Registry ID
IRCT201010034861N1
Enrollment
50
Registered
2010-10-25
Start date
2010-05-22
Completion date
Unknown
Last updated
2018-02-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Male Infertility. Male Infertility

Interventions

Intervention 1: Intervention: Red Grape Seed Extract, Capsule 300mg, Twice/day, for 3 months. Intervention 2: Control: Placebo, Capsule 300mg, Twice/day, for 3 months.
Treatment - Drugs
Placebo
Intervention: Red Grape Seed Extract, Capsule 300mg, Twice/day, for 3 months
Control: Placebo, Capsule 300mg, Twice/day, for 3 months

Sponsors

Royan Institute
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
20 Years to 45 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: Oligozoospermia with sperm count 5-20 million/ml and astenozoospermia with progressive motility less than 40% Exclusion criteria: Explained infertility (e.g. hormonal disorders, epididimis canal obstruction, epididimorchitis,...) smoking, drug or alcohol addiction, diabetes, renal disorders (creatinine more than 2.0 times), chronic liver diseases (transaminase more than twice as much normal), varicocele, infectious diseases indicated with fever and leukocytosis, sexual arousing-drugs consumption

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Sperm Motility. Timepoint: before intervention and a week after intervention. Method of measurement: Motility velocity and percentage.;ROS (Reactive Oxygen Species) levels. Timepoint: before intervention and a week after intervention. Method of measurement: Concentration assay by chemiluminesence method.;Sperm Concentration. Timepoint: before intervention and a week after intervention. Method of measurement: Counting the sperms.

Secondary

MeasureTime frame
FSH level. Timepoint: Befor intervention and a week after intervention. Method of measurement: ELISA.;LH level. Timepoint: Befor intervention and a week after intervention. Method of measurement: ELISA.;Testosterone level. Timepoint: Befor intervention and a week after intervention. Method of measurement: ELISA.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactReza Salman Yazdi

Royan Institute

r_salman_yazdi@yahoo.com+98 21 2230 6478

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026