Comparison of oral tamsulosin with oral tamsulosin and oral isosorbide dinitrate with in improvements trial without catheter (TWOC) for patients with acute urinary retention due to benign prostatic hyperplasia (BPH)

Phase 2

• Conditions: Acute urinary retention.; Retention of urine

• Registration Number: IRCT2017041724606N3
• Lead Sponsor: Vice chancellor for researche, Mazandaran University of Medical Siences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 22 February 2018

Recruitment & Eligibility

• Status: Complete
• Sex: Male
• Target Recruitment: 76

Inclusion Criteria

patients with acute urinary retention caused by benign prostatic hypertrophy(BPH).
Exclusion criteria: end stage renal disease; diabetes; history of urinary system surgery; malignancy; contraindication of tamsulusin and isosurbid consumption.

Exclusion Criteria

Not provided

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Try of urination without a catheter(TWOC). Timepoint: 72 hours after intervention. Method of measurement: Observe of urination without a catheter(TWOC).

Secondary Outcome Measures

Name	Time	Method
Vertigo. Timepoint: 72 hours after intervention. Method of measurement: Observation.;Blood pressure. Timepoint: 72 hours after intervention. Method of measurement: Sphygmomanometer(mmHg).