Description
Inclusion Criteria:
- * Central diabetes insipidus (based on routine clinical practice, e.g., clinical symptoms, serum and urinary sodium and osmolality levels or the water deprivation test)
- * Normal FT4 or T4
- * Stable hormone replacement (no change in dose of hormone replacement in six weeks prior to baseline)
Exclusion Criteria:
- * Active substance use disorder within the last 6 months
- * History of psychosis
- * Current suicidal ideation
- * Medication changes within 4 weeks of enrollment or during the study
- * History of cardiac disease, including arrhythmias, coronary heart disease, coronary artery spasms, valvular heart disease, hypertrophic cardiomyopathy (hypertension is not exclusionary)
- * Hyponatremia
- * Creatinine \>1.5mg/dL.
- * ALT or AST \>2.5x upper limit of normal
- * Hematocrit less than 2% below the norm
- * Pregnancy or breastfeeding within the last 8 weeks
- * Unwilling to use a medically acceptable form of contraception throughout the study period (female of child-bearing potential only)
- * Received an investigational drug or medical device in the past 30 days or within 5 half-lives of main study visit or be concurrently enrolled in another investigational product clinical trial.
- * Any significant illness or condition that the Investigator determines could interfere with study participation, data collection, or safety
Ages Eligible for Study:
18 Years to 60 Years (ADULT)
Sexes Eligible for Study: ALL
Accepts Healthy Volunteers:
No