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Application of special thickening condom in the treatment of premature ejaculation

Application of special thickening condom in the treatment of premature ejaculation

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200057934
Enrollment
Unknown
Registered
2022-03-22
Start date
2022-04-01
Completion date
Unknown
Last updated
2023-11-21

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

Conditions

premature ejaculation

Interventions

Group 1 :special thickening condom
Group 2:common condom

Sponsors

The First Affiliated Hospital, Zhejiang University School of Medicine
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
18 Years to 30 Years

Inclusion criteria

Inclusion criteria: 1. All patients were married or cohabiting, and had stable and regular sex life; 2. The patient or spouse is not satisfied with the incubation period of ejaculation and tries to prolong it; 3. The course of disease ranged from 6 months to 12 years, with normal prostate volume and normal sex hormone levels.

Exclusion criteria

Exclusion criteria: 1. None of the patients had serious diseases of nervous system, endocrine system, cardiovascular system, genital system or other diseases that seriously affected sexual function; 2. Have not used any sex hormone, psychotropic or cardiovascular drugs in the past 3 months; 3. No erectile dysfunction or other serious physical diseases; 4. No associated impotence.

Design outcomes

Primary

MeasureTime frame
Penile biological shock sensory threshold ;

Countries

China

Contacts

Public ContactYu Jianjun

The First Affiliated Hospital, Zhejiang University School of Medicine

yujj917@163.com+86 15158844956

Outcome results

None listed

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