Skip to content

A Clinical Study on the Combined Use of Abdominal Four Needles and Regulating the Spirit Acupuncture Method for the Treatment of Type III Chronic Prostatitis

A Clinical Study on the Combined Use of Abdominal Four Needles and Regulating the Spirit Acupuncture Method for the Treatment of Type III Chronic Prostatitis

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2026001355
Enrollment
Unknown
Registered
2026-05-26
Start date
2026-05-27
Completion date
Unknown
Last updated
2026-06-01

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

Conditions

Type III chronic prostatitis

Interventions

Experimental Group:Acupuncture
Control Group:Tamsulosin Hydrochloride Controlled-Release Capsules

Sponsors

Shanghai Research Institute of Acupuncture and Meridian
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
18 Years to 55 Years

Inclusion criteria

Inclusion criteria: (1) Meets the Western medical diagnostic criteria for Type III chronic prostatitis and the Traditional Chinese Medicine diagnostic criteria for chronic prostatitis with a pattern of damp-heat and blood stasis, with a disease duration of >3 months; (2) Male, aged 18–55 years; (3) NIH-CPSI score =15; (4) HAMD score =8 or HAMA score =8; (5) No other medications for chronic prostatitis have been taken within the past month, and no other treatments for chronic prostatitis have been received; (6) Willing to participate in this study and sign an informed consent form. Translated with DeepL.com (free version)

Exclusion criteria

Exclusion criteria: (1) Acute prostatitis or chronic bacterial prostatitis; (2) Conditions that may cause perineal pain or urinary tract irritation, such as urinary tract infections, urinary stones, diseases of the testicles, epididymis, or spermatic cord, urinary tract tumors, urethral obstruction, overactive bladder, or neurogenic bladder; (3) Patients with conditions affecting lower urinary tract function, such as senile dementia, spinal cord injury, acute or sequelae of cerebrovascular disease, multiple sclerosis, Parkinson's disease, and multiple system atrophy; (4) Patients with severe primary diseases of the heart, brain, liver, or hematopoietic system; (5) Patients with a history of psychiatric disorders or significant cognitive impairment who are unable to cooperate with treatment or complete efficacy assessments; (6) Patients with known contraindications to acupuncture treatment, such as spontaneous bleeding or uncontrolled bleeding following injury, skin infections, or ulcers; or patients with known drug allergies to tamsulosin hydrochloride sustained-release capsules.

Design outcomes

Primary

MeasureTime frame
NIH-CPSI;

Secondary

MeasureTime frame
International Prostate Symptom Score,IPSS;Visual Analogue Scale, VAS;Hamilton Depression Rating Scale,HAMD;Hamilton Anxiety Rating Scale, HAMA;Traditional Chinese Medicine (TCM) Syndrome Scoring Scale;prostate ultrasound;Residual urine ultrasound;urine flow rate;5-HT;IL-1ß;TNF-a;

Countries

China

Contacts

Public ContactLiu Hui Rong

Shanghai Research Institute of Acupuncture and Meridian

lhr_tcm@139.com13816024323

Outcome results

None listed

Source: ITMCTR (via WHO ICTRP) · Data processed: Jun 11, 2026