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A study to evaluate the validity and reliability of instrument of pattern identification for Benign Prostatic Hyperplasia and to analyze correlation between IPSS, uroflowmetry, the remaining urine amounts, sasang constitution

A study to evaluate the validity and reliability of instrument of pattern identification for Benign Prostatic Hyperplasia and to analyze correlation between IPSS, uroflowmetry, the remaining urine amounts, sasang constitution

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
CRIS
Registry ID
KCT0002345
Enrollment
56
Registered
2017-06-02
Start date
2017-03-23
Completion date
Unknown
Last updated
2019-03-11

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

Conditions

None listed

Interventions

None listed

Sponsors

Dunsan Korean Medicine Hospital of Daejeon University
Lead Sponsor

Eligibility

Sex/Gender
Male

Inclusion criteria

Inclusion criteria: - Men over 50 -Complaints of lower urinary tract symptoms, which refer to storage symptoms(urine frequency more than 8 times a day, nocturia, urgency) and voiding symptoms(hesitancy, intermittency, straining) -Ultrasonically sized prostate larger than 25g or diagnosed with benign prostatic hyperplasia

Exclusion criteria

Exclusion criteria: -Prostate cancer, prostatitis syndrome, bladder tumor, urinary stone, urethral stricture, bladder neck structure, lower urinary tract (bladder, urethral) inflammation, urinary tuberculosis -Diagnosed as a neurogenic bladder due to cerebrovascular disease, brain tumor, cerebral palsy, Parkinson's disease, multiple system atrophy, multiple sclerosis, spinal cord injury, autonomic nerve hyperreflexia, spinal cord dysplasia, pelvic surgery, herpes virus infection or diabetes - Prostate specific antigen level = 10 ng / mL - A man who refuse to accept participation in research - A person who is considered to be ineligible for participation in clinical trials due to the test result or other reasons

Design outcomes

Primary

MeasureTime frame
reliability of instrument of pattern identification for Benign Prostatic Hyperplasia;validity of instrument of pattern identification for Benign Prostatic Hyperplasia; analyze correlation between IPSS, uroflowmetry, the remaining urine amounts, sasang constitution and instrument of pattern identification for Benign Prostatic Hyperplasia

Secondary

MeasureTime frame
analyze correlation between tongue diagnosis, pulse diagnosis and instrument of pattern identification for Benign Prostatic Hyperplasia

Countries

Korea, Republic of

Contacts

Public Contactchungsik cho

Dunsan Korean Medicine Hospital of Daejeon University

choo1o2@dju.kr+82-42-470-9135

Outcome results

None listed

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