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Clinical Trials/JPRN-jRCTs051190080
JPRN-jRCTs051190080
Recruiting
Phase 4

Electroencephalography-based investigation of the effects of oral desmopressin on improving slow-wave sleep time in nocturnal polyuria patients - The DISTINCT study

Torimoto Kazumasa0 sites20 target enrollmentDecember 9, 2019

Overview

Phase
Phase 4
Intervention
Not specified
Conditions
Not specified
Sponsor
Torimoto Kazumasa
Enrollment
20
Status
Recruiting
Last Updated
2 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
December 9, 2019
End Date
TBD
Last Updated
2 years ago
Study Type
Interventional
Sex
Male

Investigators

Sponsor
Torimoto Kazumasa

Eligibility Criteria

Inclusion Criteria

  • 1 Nocturnal urinary frequency \= and \>2 and Nocturnal polyuria index (nocturnal urinary volume/24 hours urinary volume) \= and \>0\.33
  • 2 Hours of undisturbed sleep before registration \= and \<2\.5 hours
  • 3 Concentration of serum sodium \= and \>135 mEq/L
  • 4 Creatinine clearance or eGFR (estimate glomerular filtration rate) \= and \>50 mL/min/1\.73m^2

Exclusion Criteria

  • 1 Hyponatremia or the history (Concentration of serum sodium \<135 mEq/L)
  • 2 Habitual or Psychogenic polydipsia
  • 3 Heart failure or the history or suspected heart failure
  • 4 Fluid retention that requires diuretic treatment or the history
  • 5 Antidiuretic hormone incompatible secretion syndrome
  • 6 Moderate or severe renal failure (Creatinine clearance or eGFR \<50 mL/min/1\.73m^2\)
  • 7 Hypersensitivity to desmopressin or the history
  • 8 During or scheduled administration of thiazides, thiazide\-like diuretics, loop diuretics
  • 9 During or scheduled administration of corticosteroids
  • 10 Carciac pacemaker implantation

Outcomes

Primary Outcomes

Not specified

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