Study of Minirin Melt® in Adult Patients With Nocturia

Ferring

Status: Terminated

Conditions: Nocturia

Treatments: Drug: Desmopressin

Study type: Observational

Funder types: Industry

Identifiers

NCT03089073

000208

Details and patient eligibility

About

Observation of safety and efficacy of Minirin Melt® in adult patients with nocturia

Enrollment: 835 patients

Sex: All

Ages: 19 to 65 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Adult aged between 19 and 65 years
• Patients having nocturia
• Decision made to prescribe Minirin Melt according to prescription information
• Willingness and ability to provide written informed consent

Exclusion criteria

• When patients have habitual or psychogenic polydipsia (resulting in a urine production exceeding 40ml/kg/24hours)
• When patients have a history of known or suspected cardiac insufficiency and other conditions requiring treatment with diuresis
• When patients have moderate and severe renal insufficiency (creatinine clearance below 50ml/min)
• When patients have known hyponatremia
• When patients have secretion Syndrome of Inappropriate Antidiuretic Hormone Secretion (SIADH)
• When patients have hypersensitivity to the active substances or to any of the excipients