The clinical research of lumbar sympathetic ganglion block in the treatment of intractable premature ejaculation

Status

Recruiting

Phases

Early Phase 1

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR2100054840

Enrollment

Unknown

Registered

2021-12-28

Start date

2021-12-28

Completion date

Unknown

Last updated

2022-12-12

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

Conditions

Premature ejaculation

Interventions

intervention group:lumbar sympathetic ganglion block

Eligibility

Sex/Gender

Male

Age

25 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1. 25-60-year-old male, diagnosed with primary premature ejaculation, no obvious improvement after regular drug treatment for 1 month, poor effect of other treatments, strong intention to seek treatment; 2. Understand the treatment content and have signed the informed consent.

Exclusion criteria

Exclusion criteria: 1. Patients with other primary diseases of the urinary system, endocrine diseases, nervous system diseases and mental system diseases; 2. Patients with allergies to anesthetics, puncture site infection, and various preoperative examinations who are not suitable for surgery.

Design outcomes

Primary

Measure	Time frame
Premature ejaculation diagnosis tool;Intravaginal ejaculation latency time;	—

Countries

China

Contacts

Public ContactDeng Chunhua

The First Affiliated Hospital of Sun Yat-Sen University

13501519349@163.com+86 13501519349

Outcome results

None listed

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