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Efficacy of pudendal nerve pulsed radiofrequency combined with ganglion impar block for the analgesia treatment of chronic pelvic pain

Efficacy of pudendal nerve pulsed radiofrequency combined with ganglion impar block for the analgesia treatment of chronic pelvic pain

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200061800
Enrollment
Unknown
Registered
2022-07-02
Start date
2023-05-01
Completion date
Unknown
Last updated
2023-05-15

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

Conditions

Pudendal neuralgia, Chronic pelvic pain

Interventions

pudendal nerve pulsed radiofrequency combined with ganglion impar block:pudendal nerve pulsed radiofrequency combined with ganglion impar block
pudendal nerve pulsed radiofrequency:pudendal nerve pulsed radiofrequency

Sponsors

West China Hospital, Sichuan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 85 Years

Inclusion criteria

Inclusion criteria: (1) Non-cyclical, chronic pelvic pain localized in the anterior abdominal wall, umbilicus, posterior lumbosacral region, buttocks, and pudendal nerve distribution area of the anatomical pelvis for more than 6 months. (2) Voluntary participation and pain score according to the Digital Analogue Scale (VAS)=4 (3) 50% reduction in pain in the pudendal nerve distribution area or after pudendal nerve block (4) Patients aged between 18-85 years

Exclusion criteria

Exclusion criteria: (1)Participated in other clinical trials within 3 months (2)Patients who are pregnant or planning to become pregnant (3)There are patients with heart disease (4)Patients with nerve damage (5)Patients who are allergic to local anesthetics (6)Active or recurrent urinary tract infections (more than 5 times in the past 12 months) (7)Patients who are using anticoagulants or have coagulation dysfunction (8)Patients who are allergic to metals

Design outcomes

Primary

MeasureTime frame
VAS score of Pain after treatment;

Secondary

MeasureTime frame
Complications after treatment;

Countries

China

Contacts

Public ContactRurong Wang

Department of Anesthesiology, West China Hospital, Sichuan University

wangrurong@scu.edu.cn+86 18980601563

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 8, 2026