None listed
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Those with maximum flow rate (Qmax) is less than 15.0mL/s and postvoid residual urine is more than 50mL due to benign prostatic hyperplasia
Exclusion criteria
Exclusion criteria: 1) Those with complete spinal cord lesion 2) Those with complete urinary retention or with an indwelling catheter 3) Those with bladder outlet obstruction or prostatic cancer or who underwent prostatic surgery 4) Those with severe cardiovascular or hepatic disorder or orthostatic hypotension or severe renal dysfunction. 5) Those who are taking 5a-reductase inhibitor, cholinergics, anti-cholinergics, alpha antagonist or agonist, beta agonist 6) Those with asthma or Parkinson disease. 7) Those who are sensitive to cholinergics or alpha-blocker 8) Those who are judged to be improper for this clinical trial.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| IPSS (International Prostate Symptom Score) | — |
Secondary
| Measure | Time frame |
|---|---|
| Average flow rate;Postvoid Residual Urine Volume | — |
Countries
Korea, Republic of
Contacts
Dongguk University Ilsan Hospital