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Clinical exploratory study on the Treatment of Type III prostatitis (Damp-heat Descending Syndrome) with Compound Jinqiancao Granules

Clinical exploratory study on the Treatment of Type III prostatitis (Damp-heat Descending Syndrome) with Compound Jinqiancao Granules

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2025001633
Enrollment
Unknown
Registered
2025-09-01
Start date
2025-10-01
Completion date
Unknown
Last updated
2025-09-15

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

Conditions

Type III prostatitis

Interventions

Compound Jinqiancao Granules Group:Compound Jinqiancao Granules

Sponsors

Institute of Basic Research in Clinical Medicine China Academy of Chinese Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
18 Years to 45 Years

Inclusion criteria

Inclusion criteria: 1)It conforms to the diagnosis of type III prostatitis; 2) In traditional Chinese medicine it is diagnosed as damp-heat descending syndrome. 3)18 years old to 45 years old; 4)10 points =NIH-CPSI score =29 points; 5) Those who voluntarily sign the informed consent form.

Exclusion criteria

Exclusion criteria: 1) Patients with pelvic region pain and abnormal urination not caused by prostatitis such as urinary tract infections benign prostatic hyperplasia urinary calculi urethral stricture prostate tumors and other diseases; 2) Those who have used drugs or other related treatments for type III prostatitis within the past two weeks; 3) Patients with severe primary diseases Including but not limited to severe diarrhea uncontrolled cardiovascular and cerebrovascular diseases (such as unstable angina pectoris severe arrhythmia acute stroke etc.) decompensated liver disease (ALT/AST > 1.5 times the upper limit of normal) severe renal insufficiency (serum creatinine > the upper limit of normal) uncontrolled malignant tumors active immune system diseases and hematological diseases (such as severe anemia) (Coagulation disorders) and other diseases that researchers consider may affect the safety of the study; 4) Those with allergic constitutions a history of allergy to the ingredients of this product and those who cannot tolerate the drug; 5) Those with severe mental illnesses (such as major depression schizophrenia etc.); 6) Patients in the preconception period; 7) Have participated in drug clinical research within the past month; 8) The researcher considers it inappropriate to participate in clinical research.

Design outcomes

Primary

MeasureTime frame
The reduction value of NIH-CPSI score;

Secondary

MeasureTime frame
Count of white blood cells and lecithin bodies in prostatic fluid;TCM symptom score;

Countries

China

Contacts

Public ContactXie Yanming

Institute Of Basic Research In Clinical MedicineChina Academy Of Chinese Medical Sciences

ktzu2018@163.com+86 139 1111 2416

Outcome results

None listed

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