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An clinical trial on the efficacy and safety of Shen Hai Long Capsule in the treatment of male asthenospermia

An clinical trial on the efficacy and safety of Shen Hai Long Capsule in the treatment of male asthenospermia

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300068385
Enrollment
Unknown
Registered
2023-02-16
Start date
2023-02-20
Completion date
Unknown
Last updated
2023-05-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

asthenospermia

Interventions

Treatment group:Shen Hai Long Capsule
Control group:Shengjing Capsule

Sponsors

Zhongnan Hospital of Wuhan University
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
22 Years to 50 Years

Inclusion criteria

Inclusion criteria: (1) Age range from 22 to 50 years old; (2) 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; (3) At least two standard semen analyses indicated that sperm concentration =15×106 /ml; Sperm normal morphology rate =4%; (4) No other Chinese and Western drugs for the treatment of oligospermia, weak and malformed spermia have been taken in the past 3 months; (5) The subject voluntarily participates and signs the informed consent.

Exclusion criteria

Exclusion criteria: (1) Varicocele, ejaculatory duct/seminal vesicle cyst, anti-sperm antibody (+); (2) Genital tract infection: seminal plasmic elastase > 1000ng/ml or leukocyte semen disease (peroxidase positive cell concentration in semen more than 1×10^6/mL); (3) Erectile dysfunction, ejaculation disorders; (4) 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); (5) Patients with allergic history or constitution to therapeutic drugs; (6) Patients who have taken drugs affecting the study within 3 months, such as antitumor and antiepileptic drugs, etc.

Design outcomes

Primary

MeasureTime frame
Forward motile sperm ratio (PR);

Secondary

MeasureTime frame
Sperm survival rate;Sperm concentration;Normal morphology rate of sperm;Seminal malondialdehyde (MDA);Seminal superoxide dismutase (SOD);

Countries

China

Contacts

Public ContactYuanzhen ZHANG

Zhongnan Hospital of Wuhan University

zhangyuanzhen@whu.edu.cn18907139066

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026