TaVNS Improves the Symptoms of Patients With Moderate to Severe CP/CPPS

Status Not yet recruiting

Clinical Trial Summary

This trial aims to evaluate the efficacy and safety of transcutaneous auricular vagus nerve stimulation (taVNS) for moderate to severe chronic prostatitis/chronic pelvic pain syndrome (CP/CPPS). This study is a prospective, randomized, controlled trial. A total of 68 patients with CP/CPPS will be recruited. After baseline assessment, the patients will be randomized into taVNS group (n = 34) and sham-taVNS group (n = 34). The intervention of two group will last for 4 weeks with a 8-week follow-up period after the treatment. The National Institutes of Health chronic Prostatitis Symptom Score index (NIH-CPSI), International Prostate Symptom Score Scale (IPSS), European quality of Life-5 Dimensions Questionnaire (EQ-5D), self-rating anxiety Scale (SAS) and self-rating depression scale (SDS) will be assessed. The adverse events during the whole study will be recorded detailedly.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT06287970
Study type	Interventional
Source	Guang'anmen Hospital of China Academy of Chinese Medical Sciences
Contact	Jiani Wu
Phone	+8613426116653
Email	jiani_wu@aliyun.com
Status	Not yet recruiting
Phase	N/A
Start date	March 15, 2024
Completion date	February 18, 2027

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