Functional bladder outletobstruction. Disorder of urinary system, unspecified
Conditions
Interventions
Intervention 1: First Intervention group: Patients in this group receive one tamsulosin capsule at a dose of 0.4 mg at night for 3 months. Intervention 2: Second Intervention group: Patients in this g
Sponsors
Esfahan University of Medical Sciences
Eligibility
Sex/Gender
Female
Age
18 Years to 65 Years
Inclusion criteria
Inclusion criteria: Women with at least 3 months of urinary incontinence Functional urinary incontinence (having an obstructive appearance or high PVR in a uroflowmetry study or a high-pressure, low-flow appearance in a urodynamic study) Age range 18 to 65 years Consent to participate in the study
Exclusion criteria
Exclusion criteria: Having a history of anatomic obstruction or catheter passage during urodynamic study Active urinary tract infection Pregnancy Use of diuretics Heypetension Genitourinary malignancies
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Flow rate. Timepoint: Before and after intervention. Method of measurement: Based on bladder tape.;Pressure at Qmax. Timepoint: Before and after intervention. Method of measurement: Based on bladder tape.;Urinary dysfunction score. Timepoint: Before and after intervention. Method of measurement: International Prostate Symptom Score (IPSS). | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactReza Kazemi
Esfahan University of Medical Sciences
Outcome results
None listed