asthenospermia
Conditions
Interventions
control group:levocarnitine oral solution+Linggui granule mimetics
treatment group:Linggui granule and levocarnitine oral solution mimetics
Sponsors
Xiyuan Hospital of China Academy of Chinese Medical Sciences, Beijing, China
Eligibility
Sex/Gender
Male
Age
22 Years to 40 Years
Inclusion criteria
Inclusion criteria: (1) Study participants must meet the diagnostic criteria of male infertility. (2) Study participants must meet the diagnostic criteria of AZS. (3) Men aged 22 to 45 years (4) The participant must sign informed consent forms
Exclusion criteria
Exclusion criteria: (1)with infertility caused by organic lesions of the reproductive system (2)with infertility caused by the inability to complete sexual intercourse, including but not limited to erectile dysfunction, ejaculatory disorder (3)with reproductive system infection, such as chlamydia trachomatis or mycoplasma infection (4)with abnormal sex hormone (5)with palpable varicocele (6)with a history of allergy to any medicine or ingredients used in this study (7)complicated with mental diseases, malignant tumors, or serious organic diseases (8)use drugs affecting the experimental study within 3 months
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| PR sperm rate; | — |
Secondary
| Measure | Time frame |
|---|---|
| PR+NP sperm rate;spouse pregnancy rate;total effective sperm count;sperm DNA fragmentation index; | — |
Countries
China
Contacts
Public ContactGuo jun
Outcome results
None listed