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Exploration of peripheral blood immune cell heterogeneity and efficacy of Qianlie Xiaozhuo Formula in the treatment of type III chronic prostatitis patients based on single-cell RNA sequencing

Exploration of peripheral blood immune cell heterogeneity and efficacy of Qianlie Xiaozhuo Formula in the treatment of type III chronic prostatitis patients based on single-cell RNA sequencing

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600117132
Enrollment
Unknown
Registered
2026-01-20
Start date
2026-02-01
Completion date
Unknown
Last updated
2026-01-27

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

Treatment group:Qianlie Xiaozhuo Formula, composition: Anemarrhena 10g, Phellodendron 12g, Chuanxiong 12g, Angelica Dahurica 10g, Raw Astragalus 20g, Corydalis 10g, Cyperus 10g, Dryopteris 15g, Diosco
Control group:Tamsulosin hydrochloride sustained-release capsules, 0.2 mg qn, for 4 consecutive weeks.

Sponsors

Shunyi Hospital of Traditional Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
20 Years to 50 Years

Inclusion criteria

Inclusion criteria: 1. Patients aged 20 to 50 years old; 2. Not taking medications such as Qianlie Antong Capsules, Qianlie Tai Capsules, Qianlie Xin Capsules, etc. to treat the disease within one week before treatment; 3. Evaluation of indicators related to chronic prostatitis: PHQ-9 depression score >= 5 points, GAD-7 anxiety score >= 5 points, IIEF-5 score <= 21 points. 4. Meets the diagnostic criteria for type III CP set by the National Institutes of Health (NIH) and the Chinese Guidelines for Diagnosis and Treatment of Urological and Andrological Diseases (2019 edition); 5. Complies with the syndrome criteria for damp heat and stasis syndrome in the Clinical Research Guidelines for the Treatment of Chronic Prostatitis with Traditional Chinese Medicine; 6. The process of signing informed consent, voluntarily participating in the trial, and obtaining informed consent should comply with GCP regulations.

Exclusion criteria

Exclusion criteria: 1. Recurrent lower urinary tract infections, or suffering from testicular and epididymitis, varicocele, severe urethral stricture, etc; 2. Combined with basic diseases such as benign prostatic hyperplasia, prostate tumors, severe cardiovascular and cerebrovascular diseases, respiratory system diseases, liver and kidney dysfunction, etc; 3. Merge other severe systemic infections; 4. Patients who cannot obtain fully informed consent due to intellectual or behavioral impairments; 5. Patients with a history of alcohol and drug abuse, suspected or confirmed; 6. Patients who are prone to loss to follow-up, according to the researchers' judgment, may have a lower likelihood of inclusion or be complicated by other lesions; 7. Patients who have experienced dizziness with needles or blood in the past, or have a slow coagulation process after blood drawing, or are sensitive to pain and unable to complete blood drawing. 8. Patients who have ever had allergic reactions to oral Chinese medicine or traditional Chinese patent medicines and simple preparations, such as skin rash, itching, redness, dyspnea, nausea, vomiting, diarrhea and other symptoms.

Design outcomes

Primary

MeasureTime frame
NIH-CPSI Points;

Secondary

MeasureTime frame
Traditional Chinese Medicine Syndrome Score;PHQ-9 Depression Score;GAD-7 Anxiety Score;IIEF-5 Score;Urine Routine;Prostate Massage Fluid Routine;

Countries

China

Contacts

Public ContactSheng Deng

Shunyi Hospital of Traditional Chinese Medicine

dengsheng358@sina.com+86 135 2226 4993

Outcome results

None listed

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