Efficacy and Safety of Desmopressin Melt for the Treatment of Nocturia
Nocturia
About this trial
This is an interventional treatment trial for Nocturia
Eligibility Criteria
Inclusion Criteria
- Written informed consent prior to the performance of any study-related activity.
- Patients 18 years and older with an average of ≥ 2 nocturnal voids per night as determined by a 3 day frequency-volume chart during the screening period.
Exclusion Criteria:
Males:
- Clinical suspicion of bladder outlet obstruction and/or urine flow < 5 ml/s. If medical history and/or physical examination suggest bladder outlet obstruction, uroflowmetry should be performed to confirm the diagnosis
Surgical treatment for bladder outlet obstruction/benign prostatic hyperplasia performed within the past 6 months
Females:
- Pregnancy. Females of reproductive age must have documentation of a reliable method of contraception.
- Use of pessary for pelvic prolapse.
Unexplained pelvic mass.
Males and Females:
- Clinical suspicion of urinary retention and/or post void residual volume > 150 ml. If medical history and/or physical examination suggest urinary retention, bladder ultrasound or catheterization should be performed to confirm the diagnosis.
- Current or past urologic malignancy (e.g., bladder cancer, prostate cancer).
- Clinical evidence of current genitourinary tract pathology that could interfere with voiding.
- History of neurogenic detrusor activity (previously known as detrusor hyperreflexia).
- Suspicion or evidence of cardiac failure.
- Uncontrolled hypertension.
- Uncontrolled diabetes mellitus.
- Renal insufficiency. Serum creatinine must be within normal limits and estimated glomerular filtration rate (eGFR) >=60 mL/min.
- Active hepatic and/or biliary disease. Aspartate transaminase (AST) or alanine transaminase (ALT) should not be >2 times the upper limit of normal. Total bilirubin should not be > 1.5 mg/dL.
- Hyponatremia. Serum sodium level must be within normal limits
- Syndrome of Inappropriate antidiuretic hormone secretion (SIADH).
- Diabetes insipidus (urine output > 40 ml/kg over 24 hours) as determined by the 3-day voiding diary.
- Psychogenic or habitual polydipsia
Obstructive sleep apnea
Other
- Known alcohol or substance abuse
- Work or lifestyle potentially interfering with regular nighttime sleep (e.g., shift workers)
- Previous desmopressin treatment for nocturia.
- Any other medical condition, laboratory abnormality, psychiatric condition, mental incapacity or language barrier that, in the judgment of the investigator, could impair patient participation in the trial.
- Use of loop diuretics (furosemide, torsemide, ethacrynic acid). Other classes of diuretics (thiazides, triamterene, chlorthalidone, amiloride, indapamide) were permitted, either as monotherapy or combination therapy. Subjects using a diuretic were to be encouraged to take it in the morning, if medically feasible.
- Use of any other investigational drug within 30 days of screening.
Concomitant Medications
The following medications are permitted provided that the subject has been on a stable dose for the 3 months prior to the screening date (i.e. treatment has not been initiated or discontinued and there has been no change in dose):
- Alpha-blockers: Cardura (doxazosin); Flomax (tamsulosin); Hytrin (terazosin); Uroxatral (alfuzosin)
- 5 alpha-reductase inhibitors: Avodart (dutasteride); Proscar (finasteride)
- Antispasmodic, anticholinergic, antimuscarinic therapy for overactive bladder: Detrol, Detrol LA (tolterodine); Ditropan, Ditropan XL (oxybutynin); Enablex (darifenacin); Levsin(hyoscyamine); Oxytrol transdermal (oxybutynin); Sanctura (trospium); Vesicare (solifenacin)
- Sedative/hypnotic medications for sleep disorders
- Selective serotonin and mixed norepinephrine/serotonin reuptake inhibitors: Celexa (citalopram); Cymbalta (duloxetine); Effexor (venlafaxine); Lexapro (escitalopram); Paxil(paroxetine); Prozac (fluoxetine); Zoloft (sertraline)
- Chronic use of nonsteroidal anti-inflammatory agents
- Diabinese (chlorpropamide)
- Carbamazepine (carbatrol/tegretol)
- Amiodarone
Sites / Locations
- Radiant Research
- Radiant Research
- Arkansas Primary Care Clinic
- Advanced Urology Medical Center
- Impact Clinical Trials
- Atlantic Urology Medical Group
- California Professional Research
- San Diego Uro-Research
- Radiant Research
- West Coast Clinical Research
- Western Clinical Research
- Urology Associates PC
- Downtown Women's Health Care
- Genitourinary Surgical Consultants
- Connecticut Clinical Research Center, LLC
- South Florida Medical Research
- Women's Medical Research Group, LLC
- Medsearch Professional Group
- Sunrise Medical Research
- Radiant Research
- Southeastern Research Group, Inc.
- Tampa Bay Urology
- Radiant Research
- Southeastern Medical Research Institute
- Investigational site - PC
- Accelovance
- Radiant Research, Kansas City
- Benchmark Research
- Regional Urology, LLC
- Pierremont Women's Clinic
- FutureCare Studies, Inc.
- Radiant Research Inc.
- Women's Clinic of Lincoln, P.C
- Investigational site
- AdvanceMed Research
- Lawrenceville Urology
- Morristown Urology
- Urology Group of New Mexico, PC
- Upstate Urology
- Investigational site - Adult & Pediatric Urology
- AccuMed Research Associates
- University Urology Associates
- Ferring Pharmaceutical Inc
- Northeast Urology Research
- PharmQuest
- New Hanover Medical Research
- Piedmont Medical Research Associates
- Radiant Research
- Radiant Research - Akron
- Urologic Consultants of SE PA
- Philadelphia Clinical Research, LLC
- Radiant Research
- Advanced Clinical Concepts
- University Medical Group
- Radiant Research, Greer
- Palmetto Medical Research
- Carolina Urologic Research Center
- Holston Medical Group
- Vanderbilt University Medical Center
- Advanced Research Associates
- Health Central Women's Care
- Accelovance
- Regional Medical Center and Diagnostic
- Radiant Research San Antonio
- Urology San Antonio Research, PA
- Virginia Urology Center
- Urology of Virginia PC
- Women's Clinical Research Center
- Investigational site - Medical Professional
- Seattle Urology Research Center
- Southern Interior Medical Center
- Can-Med Clinical Research Inc.
- Investigational site - Clinical Research
- Investigational site - Professional Corporation
- The Male/Female Health and Reserach
- Brantford Urology Research
- Guelph Urology Associates
- Investigational site
- The Fe/Male Health Centres
- Sunnybrook Health Sciences Centre
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm 4
Arm 5
Placebo Comparator
Experimental
Experimental
Experimental
Experimental
Placebo
desmopressin melt 10 μg
desmopressin melt 25 μg
desmopressin melt 50 μg
desmopressin melt 100 μg
Participants took a placebo 'melt' for 28 days to complete part 1 of the study. In part 2, placebo patients were randomized to one of the other 4 treatment arms based on assignments predetermined at the initial randomization, to receive active desmopressin melt for between 1 and 6 months (until the database for part 1 was locked and treatment was unblinded).
Participants took desmopressin melt 10 μg for 28 days to complete part 1 of the study. Participants continued on this dose in part 2 of the study for between 1 and 6 months (until the database for part 1 was locked and treatment was unblinded).
Participants took desmopressin melt 25 μg for 28 days to complete part 1 of the study. Participants continued on this dose in part 2 of the study for between 1 and 6 months (until the database for part 1 was locked and treatment was unblinded).
Participants took desmopressin melt 50 μg for 28 days to complete part 1 of the study. Participants continued on this dose in part 2 of the study for between 1 and 6 months (until the database for part 1 was locked and treatment was unblinded).
Participants will take desmopressin melt 100 μg for 28 days to complete part 1 of the study. Participants will continue on this dose in part 2 of the study for between 1-6 months (until the database for part 1 is locked and treatment is unblinded).