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Clinical research on effectiveness and safety of azoospermia or severe oligozoospermia treated with uFSH

Clinical research on effectiveness and safety of azoospermia or severe oligozoospermia treated with uFSH

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-IPR-14005647
Enrollment
Unknown
Registered
2014-12-10
Start date
2014-08-02
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

severe oligospermia or azoospermia

Interventions

1:75IU uFSH (Livzon Pharm Group Inc., China) being injected into patients every 3 days for 6 months
2:75IU uFSH (Livzon Pharm Group Inc., China) being injected into patients every 3 days for 6 months

Sponsors

Peking University Third Hospital
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
20 Years to 35 Years

Inclusion criteria

Inclusion criteria: Male subjects aged 20~35; They accorded with diagnostic criteria of severe oligospermia or azoospermia; They had'nt been treated with drug which could improve sperm count and quality one month before observation, otherwise, they should have a elution for 1 month before the study.

Exclusion criteria

Exclusion criteria: Gram-positive bacteria, Chlamydia trachomatis, Ureaplasmaurealyticum, or mycoplasma hominis were detected in their semen; Subjects addicted to drug, tobacco, or alcohol; Subjects had heat, chemicals, radioactive material, or toxic contact history within a year; Subjects were under treatment of gonadotropin,anabolic steroid, chemotherapeutic drugs, or nonsteroidal anti-inflammatory drugs; Subjects combined with cardiovascular, liver, kidney, or hematopoietic system severe primary disease, or mental disease; Subjects were allergic or on uFSH allergy, or under the treatment of other drugs for infertility; Subjects did not meet the inclusion criteria, did not according to the prescribed medication, were unable to judge the efficacy, had incomplete information, or affected the efficacy or safety judgment; Subjects were IHH patients.

Design outcomes

Primary

MeasureTime frame
hormonal level in vivo;testicular volume;sperm density;sperm motility of level (a+b);sperm of level a;semen volume;

Countries

China

Contacts

Public ContactJiang Hui
jianghui55@163.com+86 13910776509

Outcome results

None listed

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