DRUG
Desmopressin Acetate
This arm will receive tamsulosin and desmopressin acetate daily a
Status
Unknown
Phase
Phase 4
Enrollment
160
Locations
1
Results
Not posted
Publications
0
Study summary
In this study investigators will add desmopressin for treatment of patients with benign prostatic hyperplasia and nocturnal polyurea
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
DRUG
This arm will receive tamsulosin and desmopressin acetate daily a
DRUG
This arm will receive tamsulosin and placebo
Timeline
First posted
Jul 14, 2023
Study start
Jul 20, 2023
Primary completion
Jan 10, 2024
Study completion
Feb 10, 2024
Results posted
Not reported
Registry updated
Jul 14, 2023
Outcomes
Change of symptoms and nocturia disappears or improve
Time frame · Follow up for 6 months
Investigators will compare symptoms in the pretreatment period and follow up symptoms following treatment and record the outcome
Not reported in the indexed record.
Eligibility
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
Study locations
Egypt. Showing up to 24 locations stored in the fast local snapshot.
Urology and nephrology center
Al Mansurah, Outside U.S./Canada, Egypt
Publications
No PMID-linked publications were present in this registry snapshot.
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