Study Of Therapeutic Effect Of Desmopressin In The Treatment Of Nocturia In The Patients Who Referred To Urology Ward Of 501 I.R.I Army Hospital
Not Applicable
- Conditions
- octuria.Nocturia
- Registration Number
- IRCT201010234989N1
- Lead Sponsor
- I.R.I Army University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- Male
- Target Recruitment
- 60
Inclusion Criteria
Nocturnal voiding at least 2 times or more
Exclusin criteria: Drug noncompliance, uncontrolled diabetes mellitus, decompensated heart failure, Neurogenic bladder, Diabetes insipidus
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method octurnal Voiding Frequency. Timepoint: Before intervention, 4 weeks after intervention, 8 weeks after intervention. Method of measurement: Interview with patient.
- Secondary Outcome Measures
Name Time Method Drug Adverse Effects. Timepoint: Before intervention, 4 weeks after intervention, 8 weeks after intervention. Method of measurement: Interview with patient.