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Evaluation of efficacy and safety of terazosin in patients with benign prostatic hyperplasia with lower urinary tract symptoms

Not Applicable
Conditions
Diseases of The genitoruinary system
Registration Number
KCT0005278
Lead Sponsor
Yonsei University, Wonju Severance Christian Hospital
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot yet recruiting
Sex
Male
Target Recruitment
174
Inclusion Criteria

(1) Male over 40 years old
(2) A person with an IPSS total score of 8 or higher
(3) Those whose maximum urine velocity (Qmax) is less than 10mL/s
(4) Those who have a single void volume of 150 mL or more
(5) A person who consented to participate in this study by handwritten signature

Exclusion Criteria

(1) People who are hypersensitive to Alpha-blocker drugs
(2) People with bladder neck stenosis and urinary tract stenosis
(3) Those with renal dysfunction (creatinine concentration in serum>2.0mg/dL)
(4) People who have a severe liver disorder or have a history
(5) People with severe cardiovascular disease
(6) People with severe hypotension
(7) Other research directors judge that it is inappropriate to participate in this research

Study & Design

Study Type
Interventional Study
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Change in IPSS(International Prostate Symptom Score) total score
Secondary Outcome Measures
NameTimeMethod
Change in OABSS(Overactive Bladder Symptom Score) total score;Change in Qmax and Qave;IPSS (International Prostate Symptom Score) Total change rate(~10%, 10-30%, 30%~);Change in IPSS-QoL(International Prostate Symptom Score-Quality of life)
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