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Adding Desmopressin to Tamsulosin for Treatment of BPH

Outcome of Adding Desmopressin to Tamsulosin for Treatment of Nocturnal Polyurea in Patients With Benign Prostatic Obstruction

Status
UNKNOWN
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05945420
Enrollment
160
Registered
2023-07-14
Start date
2023-07-20
Completion date
2024-02-10
Last updated
2023-07-14

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

Conditions

Nocturnal Polyurea in Patients With BPH

Brief summary

In this study investigators will add desmopressin for treatment of patients with benign prostatic hyperplasia and nocturnal polyurea

Detailed description

Investigators will give a group of patients tamsulosin and desmopressin and the other group will take tamsulosin and placepo and compare the outcome regarding symptoms of being prostatic hyperplasia especially nocturia and the effect on nocturnal polyurea in patients

Interventions

DRUGPlacebo

This arm will receive tamsulosin and placebo

This arm will receive tamsulosin and desmopressin acetate daily a

Sponsors

Mansoura University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
MALE
Age
50 Years to 80 Years
Healthy volunteers
Yes

Inclusion criteria

Men with BPH Age more than 50years Patients with nocturia (2voids per night or More) Patients with nocturnal polyurea (urine volume More than 33%of urine allover the day) IPSS more than 12 Obstructed flow curve Post voiding residual less than 150

Exclusion criteria

* men with BPH with : Acute urine retention Neurogenic bladder dysfunction Cardiovascular disease Hyponatremia Urethral stricture Bladder calculi Prostate cancer

Design outcomes

Primary

MeasureTime frameDescription
Change of symptoms and nocturia disappears or improveFollow up for 6 monthsInvestigators will compare symptoms in the pretreatment period and follow up symptoms following treatment and record the outcome

Countries

Egypt

Contacts

Primary ContactAhmed Azmy, Resident
dr.a.azmy93@gmail.com+20 01010623936

Outcome results

None listed

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