Shen Hai Long Capsule for Male Asthenospermia
Efficacy and Safety of Shen Hai Long Capsule for Mild to Moderate Asthenospermia in Men
About this trial
This is an interventional treatment trial for Efficacy and Safety of Shen Hai Long Capsule for Mild to Moderate Asthenospermia in Men focused on measuring efficacy, safety
Eligibility Criteria
Inclusion Criteria: Age range from 22 to 50 years old; Patients with mild to moderate asthenospermia, that is, at least two normative semen analyses indicated that 10%≤PR percentage < 32% and the total number of PR sperm ranged from 5 million to 20 million; At least two standard semen analyses indicated that sperm concentration ≥15×106 /ml; Sperm normal morphology rate ≥4%; No other Chinese and Western drugs for the treatment of oligospermia, weak and malformed spermia have been taken in the past 3 months; The subject voluntarily participates and signs the informed consent. Exclusion Criteria: Varicocele, ejaculatory duct/seminal vesicle cyst, anti-sperm antibody (+); Genital tract infection: seminal plasmic elastase > 1000ng/ml or leukocyte semen disease (peroxidase positive cell concentration in semen more than 1×10^6/mL); Erectile dysfunction, ejaculation disorders; suffer from mental disorders, immune system diseases; Severe impairment of liver and kidney function (serum transaminase ≥2× upper limit of medical reference value, creatinine clearance ≤40ml/min or active stage of chronic kidney disease); Patients with allergic history or constitution to therapeutic drugs; Patients who have taken drugs affecting the study within 3 months, such as antitumor and antiepileptic drugs, etc.
Sites / Locations
- Zhongnan Hospital of Wuhan University
Arms of the Study
Arm 1
Arm 2
Experimental
Active Comparator
Shen Hai Long Group
Sheng Jing Group