male infertility
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1) Male patients who are 18 years of age or older at the time of consent 2) Patients who have visited Chiba University Hospital or Kameda IVF Clinic Makuhari with the intention of conception. 3) Patients who have received a thorough explanation of their participation in this study, and who have given written consent of their own free will based on a thorough understanding of the study.
Exclusion criteria
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)
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Changes in semen findings, sORP, DFI, microRNA expression, and diet before and after lifestyle diet modification guidance and urologic intervention | — |
Secondary
| Measure | Time frame |
|---|---|
| 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 | — |
Countries
Japan
Contacts
Chiba University Hospital Department of Urology