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Evaluating the effects of symbiotic therapy in male infertility with idiopathic oligoastenospermia

Evaluating the effects of symbiotic therapy in male infertility with idiopathic oligoastenospermia

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
IRCT
Registry ID
IRCT20190810044500N6
Enrollment
40
Registered
2020-09-05
Start date
2020-09-22
Completion date
Unknown
Last updated
2020-09-07

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

Conditions

Idiopathic oligoasthenospermia.

Interventions

Intervention 1: Intervention group:They receive FamiLact capsules once a day for 4 weeks. Intervention 2: Control group: They receive placebo once a day for 4 weeks.

Sponsors

Yazd University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
20 Years to 50 Years

Inclusion criteria

Inclusion criteria: Age 20 to 50 years Sperm concentration below 15 million per cc Percentage of progressive motile spermatozoa < 32% Total ejaculated spermatozoa<39*106 Total motility <40% Normal serum levels of free testosterone, Prolactin, Luteinizing hormone, Follicle-stimulating hormone

Exclusion criteria

Exclusion criteria: Drug or alcohol abuse Concentration of white blood cells in semen > 106 per cc Possibility of being treated with gonadotropins, anabolic steroids, cancer chemotherapy, NSAIDs, infertility medications in the last two months Previous history of chemotherapy or radiotherapy for cancer Existence of palpable varicocele X-ray history of the past eight months Y chromosome microdeletion Karyotype alterations Testicular atrophy and testicular failure Other secondary causes of infertility A history of liver problems and a history of allergy to clomiphene Percentage of typical forms<4% Ejaculated volume <1.5 ml Abnormal serum levels of free testosterone, Prolactin, Luteinizing hormone, Follicle-stimulating hormone

Design outcomes

Primary

MeasureTime frame
Sperm concentration in semen. Timepoint: Before the intervention and after the intervention. Method of measurement: Spermatogram test.;Sperm motility in semen. Timepoint: Before the intervention and after the intervention. Method of measurement: Spermatogram test.;Sperm morphology in Semen. Timepoint: Before the intervention and after the intervention. Method of measurement: Spermatogram test.;Semen fluid volume. Timepoint: Before the intervention and after the intervention. Method of measurement: Spermatogram test.;Semen fluid Power Hydrogen. Timepoint: Before the intervention and after the intervention. Method of measurement: Spermatogram test.;Serum concentration of free testosterone, prolactin, luteinizing hormone, follicle-stimulating hormone. Timepoint: Before the intervention and after the intervention. Method of measurement: Blood test.

Secondary

MeasureTime frame
Age. Timepoint: Before the intervention and after the intervention. Method of measurement: Questionnaire.;Height. Timepoint: Before the intervention and after the intervention. Method of measurement: Questionnaire.;Weight. Timepoint: Before the intervention and after the intervention. Method of measurement: Questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactFatemeh Saghafi

Yazd University of Medical Sciences

F.saghafi@ssu.ac.ir+98 35 3820 3419

Outcome results

None listed

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