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Analysis of the Effect of Preconception Care on Male Fertility

Phase 1
Recruiting
Conditions
male infertility
Registration Number
JPRN-UMIN000053075
Lead Sponsor
Chiba University Hospital
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
Male
Target Recruitment
100
Inclusion Criteria

Not provided

Exclusion Criteria

1) Patients undergoing treatment for any of the following diseases that may affect the results of the study; malignant tumors (including pre-existing), uncontrolled allergic diseases 2) Taking any of the following medications that may affect the study results; Salazopyrine, finasteride, dutasteride, other hormonal drugs, psychotropic drugs, SSRIs, SNRIs, methotrexate 3) Patients with azoospermia 4) Those who have undergone infertility treatment in the past 5) Those who have participated in other clinical trials within one month prior to obtaining consent 6) Other subjects who are deemed by the investigator to be inappropriate for the study (i.e., study implementation may increase the risk to study subjects or may not provide sufficient data)

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Changes in semen findings, sORP, DFI, microRNA expression, and diet before and after lifestyle diet modification guidance and urologic intervention
Secondary Outcome Measures
NameTimeMethod
1) Association of lifestyle and diet with primary endpoints; 2) Association of male factors with primary endpoints; 3) Correlation of primary endpoints with pregnancy rate, time to pregnancy, miscarriage rate, and live birth rate
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