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

Recruiting N/A Interventional Study
Chronic Prostatitis
No Placebo Group Every participant receives an active treatment — no one gets a placebo.
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At a Glance
Age
18 – 50
Sex
Male
Study type
Interventional
Purpose
Treatment
Participants needed
68 (estimated)
Sponsor
Jiani Wu · Other
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About This Trial
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 sh…
Trial Locations
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Eligibility Criteria
Inclusion Criteria: * Consistent with the diagnostic criteria of CP/CPPS of EAU or CAU, the clinical manifestations were recurrent and persistent prostate pain accompanied by abnormal urination and psychiatric symptoms, without infection or other obvious pathological conditions. The pain symptoms w…
Contacts

Jiani Wu

+8613426116653

jiani_wu@aliyun.com

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