Skip to content

A single-arm, self-controlled study on the efficacy and safety of a premature ejaculation training device for the treatment of premature ejaculation

A single-arm, self-controlled study on the efficacy and safety of a premature ejaculation training device for the treatment of premature ejaculation

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600116567
Enrollment
Unknown
Registered
2026-01-12
Start date
2026-01-12
Completion date
Unknown
Last updated
2026-01-27

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

Conditions

Premature ejaculation

Interventions

Experimental group:Use the premature ejaculation training device with the preset program for behavioral training twice a week.

Sponsors

Renji Hospital, Shanghai Jiaotong University School of Medicine
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
18 Years to 50 Years

Inclusion criteria

Inclusion criteria: 1) Males aged 18 to 50 with stable sexual activity; 2) Self-reported intravaginal ejaculation latency (IELT) = 11 points; 4) Normal external genitalia development; 5) No chronic diseases affecting male sexual function, such as cardiovascular and cerebrovascular diseases, liver and kidney dysfunction, mental illness, etc.

Exclusion criteria

Exclusion criteria: 1) Age 50 years; 2) Patients with moderate to severe erectile dysfunction as defined by the International Index of Erectile Function (IIEF) scale, or patients with multiple sclerosis; 3) Patients using medications that may affect intravaginal ejaculation latency time (IELT), such as SSRIs (selective serotonin reuptake inhibitors) and opioids; 4) Have a history of acute and chronic diseases that affect male sexual function, such as cardiovascular and cerebrovascular diseases, liver and kidney dysfunction, mental illness, etc.; There is a history of major trauma and surgery of the pelvic and nervous system.

Design outcomes

Primary

MeasureTime frame
IELT;

Secondary

MeasureTime frame
Premature Ejaculation Diagnostic Tool (PEDT) Questionnaire Score;

Countries

China

Contacts

Public ContactMujun Lu

Renji Hospital, Shanghai Jiaotong University School of Medicine

lumujun@163.com+86 130 2015 6427

Outcome results

None listed

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