Skip to content

Effect of Tamsulosin vs Prazosin in Treatment of Female Voiding Dysfunction

Effect of Tamsulosin vs Prazosin in Treatment of Female Voiding Dysfunction

Status
UNKNOWN
Phases
Phase 1Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00602186
Enrollment
80
Registered
2008-01-28
Start date
2005-07-31
Completion date
2008-03-31
Last updated
2008-01-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Neurogenic Bladder

Keywords

female voiding dysfunction, Tamsolusin, prazosin

Brief summary

The purpose of this study is to determine whether Tamsolusin or Prazosin are effective in the treatment of female voiding dysfunction(BOO)

Detailed description

Voiding dysfunction is not uncommon in Tabriz.About 20% of patients in female urology clinic of Tabriz university of medical sciences sufered from some degrees of voiding dysfunction (due to bladder imparement or bladder outlet obstruction).There is limited information about medical treatment of those patients. On the other hand alpha adrenergic blockers are the first choice medication in BENIGN PROSTATIC HYPERPLASIA. There is some new facts about destribution of alpha adrenergic blockers in female pelvic floor.The purpose of this study is to comparision whether Tamsolusin 0.4/daily or Prazosin 1 mg/daily are effective in the treatment of female voiding dysfunction(BOO)

Interventions

0.4 mg /day

DRUGprazosin

1 mg/day

Sponsors

Tabriz University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Outcomes Assessor)

Eligibility

Sex/Gender
FEMALE
Age
20 Years to 70 Years
Healthy volunteers
No

Inclusion criteria

* Healthy females with voiding difficulty with MFR\<12 and post void residual urine\>50cc

Exclusion criteria

* History of pelvic floor surgury during last 3 month * Any contraindication for Tamsolusin or prazosin

Design outcomes

Primary

MeasureTime frame
patient symptoms improvement(Standard questionare)every month untile 3 months

Secondary

MeasureTime frame
Urodynamics parameters improvementthree months later

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026