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
Name Time Method 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
Name Time Method