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Therapeutic effect of Xialiqi Capsule on benign prostatic hyperplasia

Phase 4
Recruiting
Conditions
benign prostatic hyperplasia
Registration Number
ITMCTR2100005234
Lead Sponsor
Second Hospital of Tianjin Medical University
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
Male
Target Recruitment
Not specified
Inclusion Criteria

1. Patients with BPH who have symptoms of frequent urination and dysuria, diagnosed by digital rectal examination, B-ultrasound, and uroflowmetry.
2. IPSS>=13 and/or QOL>=3 points.
3. Prostate volume > 25ml.
4. The maximum urine flow rate is less than 15ml/s.
5. Residual urine volume <100ml.
6. Aged > 50 years.
7. The patients voluntarily participated and signed the informed consent.
8. PSA<4ng/ml or PSA>4ng/ml, but exclude patients with prostate cancer.
9. In line with the dialectical standard of TCM spleen-kidney qi deficiency and phlegm stasis syndrome.

Exclusion Criteria

1. With other diseases that cause urination disorders, such as prostate cancer.
2. The patient or his authorizer is unwilling to comply with the study protocol.
3. Upper urinary tract hydrops, bladder stones, repeated hematuria, urinary tract infections caused by benign prostatic hyperplasia.
4. Patients with benign prostatic hyperplasia who have failed invasive treatment and who have a history of pelvic surgery or injury.
5. Patients with severe diabetes, hypertension, cardiovascular and cerebrovascular diseases.
6. Patients with major organ dysfunction, such as liver and kidney insufficiency.
7. Psychopaths.
8. Those with allergies.

Study & Design

Study Type
Interventional study
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod

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