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The effect of combination therapy of human chorionic gonadotropin ampoule (HCG) and Letrozole tablet on spermogram parameters in obese men with idiopathic infertility

Phase 2
Recruiting
Conditions
Male idiopathic infertility.
Male infertility
Registration Number
IRCT20100614004181N9
Lead Sponsor
Tabriz University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
Male
Target Recruitment
45
Inclusion Criteria

Obese men with a body mass index greater than 30
Idiopathic infertility
Age 20 to 45 years
Men with informed consent

Exclusion Criteria

Men with a history of genital surgery
Men with a history of infectious disease in the genital system
Men with symptoms of urinary or genital infection
Men with a history of suspected contact or urethritis symptoms
Men with spermatogenesis-damaging drugs such as Sulfasalazine
Men with history of tobacco and alcohol or drugs consuming
Men with a family history of infertility in first degree relatives
Men with testicular atrophy
Men with varicocele
Men with changes in consistency and size of cord and vasodefran and epididymis
Men with abnormalities in hormone or renal and liver tests
Obese men with age less than 20-year old
Obese men with age more than 45-year old
Men without informed consent

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Sperm indices including sperm volume evaluation, sperm count, motility rate and sperm morphology. Timepoint: One day before treatment and 3 months after treatment. Method of measurement: Spermogram test.
Secondary Outcome Measures
NameTimeMethod
Serum levels of testosterone. Timepoint: One day before treatment and 3 months after treatment. Method of measurement: Evaluation of venous blood sample based on laboratory kit.;Serum levels of estradiol. Timepoint: One day before treatment and 3 months after treatment. Method of measurement: Evaluation of venous blood sample based on laboratory kit.
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