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A Randomized Controlled Trial of Zangdi Babao Tablets in the Treatment of Male Infertility

A Randomized Controlled Trial of Zangdi Babao Tablets in the Treatment of Male Infertility

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500108085
Enrollment
Unknown
Registered
2025-08-25
Start date
2025-09-01
Completion date
Unknown
Last updated
2025-09-01

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

Conditions

Male Infertility

Interventions

Test Group:Take Zangdi Babao Tablets, 2 tablets each time, 3 times a day, for 12 consecutive weeks.
Control Group:Take a placebo consistent with Zangdi Babao Tablets in terms of appearance, specifications and usage, for 12 consecutive weeks.

Sponsors

Hospital for Reproductive Medicine Affiliated to Shandong University
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
20 Years to 45 Years

Inclusion criteria

Inclusion criteria: 1. Male, aged 20-45 years; 2. Meeting the diagnosis of male infertility: failure to conceive after 1 year of unprotected intercourse, with normal examination results of the female partner; 3. Baseline sperm progressive motility rate < 32%; 4. Voluntarily participating in the study and signing the informed consent form.

Exclusion criteria

Exclusion criteria: 1. Congenital malformation of the reproductive system or severe acquired injury; 2. Abnormal liver or kidney function (ALT/AST > 1.5 times the upper limit of normal); 3. Use of drugs to improve sperm quality in the past 3 months; 4. Allergy to the ingredients of Zangdi Babao Tablets; 5. Complicated with severe underlying diseases such as malignant tumors and mental illnesses.

Design outcomes

Primary

MeasureTime frame
sperm progressive motility rate;

Secondary

MeasureTime frame
serum testosterone level,;sperm deformity rate,;IIEF-15 score;

Countries

China

Contacts

Public ContactJingmei Hu

Hospital for Reproductive Medicine Affiliated to Shandong University

hujingmei77@163.com+86 151 6886 3682

Outcome results

None listed

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