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Comparison of ultrasonography and uroflowmetry in diagnosis of bladder outlet obstruction due to benign prostatic hyperplasia

Not Applicable
Conditions
Bladder outlet obstruction.
Bladder-neck obstruction
Registration Number
IRCT2016022326718N1
Lead Sponsor
rology Research Center
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
Male
Target Recruitment
250
Inclusion Criteria

patients peresenting with lower urinary tract symptom (LUTS) due to benign prostate hyperplasia (BPH)

Exclusion criteria: history of prostatitis; urinary tract surgery; trauma; Urethritis; urinary stone passage; Catheterization; abnormal prostate specific antigene (PSA) and digital rectal exam (DRE); BPH surgical criterias; Neurogenic bladder

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Prostate volume. Timepoint: During hospitalization. Method of measurement: Ultrasonography.;Urine residue. Timepoint: During hospitalization. Method of measurement: Ultrasonography.;Bladder wall thickness. Timepoint: During hospitalization. Method of measurement: Ultrasonography.;Intravesical protrusion of prostate. Timepoint: During hospitalization. Method of measurement: Ultrasonography.;Qmax. Timepoint: During hospitalization. Method of measurement: Uroflowmetery.;International Prostate Symptom Score. Timepoint: During hospitalization. Method of measurement: Based on a standard questionnaire with scores of 0 to 35.;Prostate specific antigen. Timepoint: During hospitalization. Method of measurement: Blood test.
Secondary Outcome Measures
NameTimeMethod
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