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Efficacy and Safety Evaluation of Buyu No.1 Formula in the Intervention of Varicocele Associated with Oligoasthenozoospermia

Efficacy and Safety Evaluation of Buyu No.1 Formula in the Intervention of Varicocele Associated with Oligoasthenozoospermia

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2025002328
Enrollment
Unknown
Registered
2025-11-28
Start date
2025-12-01
Completion date
Unknown
Last updated
2025-12-08

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

Conditions

Varicocele with Oligoasthenospermia

Interventions

Buyu No.1 Formula + Placebo (Tablet) Group:The treatment involves taking the kidney-tonifying Buyu No.1 Formula ready-to-drink granules and Mai Zhiling placebo tablets (as a control), with a 12-week c
B (Mai Zhiling tablets + placebo (granules) group):Treatment involves taking Mesilium tablets and Chinese herbal placebo (granules), with a 12-week course. Mesilium tablets: 2 tablets per dose, twice

Sponsors

Beijing University of Chinese Medicine Dongzhimen Hospital
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
22 Years to 50 Years

Inclusion criteria

Inclusion criteria: (1) Males aged between 22 and 50 years (inclusive of 22 and 50 years); (2) Meet the diagnostic criteria for varicocele with oligoasthenospermia; (3) Have not taken medications for the treatment of varicocele or oligoasthenospermia within the past month; (4) Are able to maintain a regular sexual life; (5) Voluntarily participate in this study and sign the informed consent form.

Exclusion criteria

Exclusion criteria: (1) Non-varicocele-associated oligoasthenozoospermia; (2) Combined with congenital malformations, underdeveloped or atrophic testes, chromosomal abnormalities, genitourinary system infections, endocrine disorders, etc.; (3) Spouse infertility; (4) Combined with abnormal liver or kidney function, neurological diseases, cardiovascular diseases, or other severe primary diseases of other systems; (5) Allergy to the drugs used in this study.

Design outcomes

Primary

MeasureTime frame
Total sperm motility (PR + NP);Sperm concentration;

Secondary

MeasureTime frame
Sperm DNA Fragmentation Index (DFI);Internal diameter of the spermatic vein;TCM syndrome score;Spouse Pregnancy Status;

Countries

China

Contacts

Public ContactWang Bin

Beijing University of Chinese Medicine Dongzhimen Hospital

bucmlkc@126.com010-8401-5602

Outcome results

None listed

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