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The preliminary prospective study of Treatment with A thiazide-based diuretic for Nocturnal polYuria associated with hypertensiO

Not Applicable
Conditions
octurnal polyuria
Registration Number
JPRN-UMIN000030330
Lead Sponsor
Department of Urology, Nara Medical University
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete: follow-up complete
Sex
All
Target Recruitment
20
Inclusion Criteria

Not provided

Exclusion Criteria

- Administration of diuretics as antihypertensive drugs - Untreated lower urinary tract dysfunction including benign prostatic hyperplasia and overactive bladder - Post-void residual urine: 100 mL and more - Chronic renal disease: G3b and more (eGFR <45 mL/min/1.73m^2) - Chronic heart failure: NYHA Class 3 or 4 - Insomnia associated with mental illness

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Change in slow wave sleep time after 4 weeks from the start of administration
Secondary Outcome Measures
NameTimeMethod
Changes after 4 weeks from the start of administration - Nocturnal polyuria index - Nocturnal urinary volume - Diurnal urinary volume - Nocturnal excretoin of sodium in urine - Diurnal excretoin of sodium in urine - Total sleep time - Sleep efficiency - Body fluid
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