Current partner codePEPTIDESDE
NCT01729819·Phase 2·INTERVENTIONAL

Interventional Clinical Trial in Patients in Overactive Bladder With Nocturia in Women

Status

Completed

Phase

Phase 2

Enrollment

106

Locations

24

Results

Posted

Publications

0

Study summary

What the protocol is testing.

The purpose of the trial is to investigate the efficacy of combining tolterodine and desmopressin compared with tolterodine monotherapy in the treatment of women with overactive bladder with nocturia in terms of reduction of nocturnal voids during 3 months of treatment

Interventions

Treatment arms and agents.

DRUG

Tolterodine tartrate extended release capsules

DRUG

Desmopressin orally disintegrating tablets

DRUG

Placebo orally disintegrating tablets

Timeline

From registration to results.

  1. First posted

    Nov 20, 2012

  2. Study start

    Jan 2013

  3. Primary completion

    Nov 2014

  4. Study completion

    Nov 2014

  5. Results posted

    Aug 14, 2018

  6. Registry updated

    Sep 12, 2018

Outcomes

What the study measures.

Primary outcomes

Change in Mean Number of Nocturnal Voids From Baseline

Time frame · Baseline to 3 months of treatment

A nocturnal void was defined as a void occurring at least 5 minutes after going to bed, but before getting up the next morning. The mean estimate was the average over 3 consecutive 24-hour periods prior to the respective visit as captured in the voiding and sleep diary.

Secondary outcomes

Change in Mean Time to First Nocturnal Void From Baseline

Time frame · Baseline to 3 months of treatment

The time to first nocturnal void was defined as the time from going to bed with the intention of sleeping until first nocturnal void or until waking in the morning in the case there is no nocturnal void. The time to first void was calculated as the average over three consecutive 24-hour periods prior to the respective visits.

Change in Mean Nocturnal Urine Volume From Baseline

Time frame · Baseline to 3 months of treatment

The mean nocturnal urine volume was derived from the three-day urine volume diary. The nocturnal volume was defined as the sum of the volumes for all nocturnal voids including the volume of the first morning void within 30 min of waking up in the morning.

Responder Status

Time frame · Baseline to 3 months of treatment

Responder status was defined as ≥33% decrease in the mean number of nocturnal void and at least one night with no voids out of the 3-day diary period.

Onset of Effect as Seen in Change in Mean Number of Nocturnal Voids From Baseline for Each Visit During Three Months of Treatment

Time frame · Baseline to 3 months of treatment

A nocturnal void was defined as a void occurring at least 5 minutes after going to bed, but before getting up the next morning. The mean estimate was the average over 3 consecutive 24-hour periods prior to the respective visit as captured in the voiding and sleep diary.

Change in the Impact on Sleep as Measured by the Sleep Rating Scales From Baseline

Time frame · Baseline to 3 months of treatment

An electronic diary was used in the trial to document the impact on sleep quality (sleep rating scales). The sleep rating scales included three questions that ranged from 0 (poor) to 10 (good). The average of each question for each visit was summarised and the change from baseline was analysed longitudinally during the three months of treatment.

Eligibility

Who can take part.

Minimum age
18 Years
Maximum age
Not reported
Sex
FEMALE
Healthy volunteers
No

Inclusion Criteria: * Written informed consent prior to performance of any trial-related activity * Female sex, at least 18 years of age (at the time of written consent) * Nocturia and overactive bladder symptoms present for ≥6 months prior to trial entry (patient-reported) * At least 2 nocturnal voids each night as documented in 2 diary periods during the screening. A mean of at least 8 daytime voids per day over 3 days with a minimum of at least 6 daytime voids each day as documented in 2 diary periods during the screening. At least 1 urgency episode each 24 hours as documented in 2 diary periods during the screening. Each diary period consists of 3 consecutive days, with at least 14 days between each period. Exclusion Criteria: * Evidence of severe voiding dysfunction defined as: More than 10 nocturnal voids per 24 hours as documented on any of the days in both diary periods during screening. More than 20 daytime voids per 24 hours as documented on any of the days in both diary periods during screening. * Genito-urinary tract pathology that can in the investigator's opinion be responsible for urgency or urinary incontinence e.g., symptomatic or recurrent urinary tract infections, interstitial cystitis, bladder related pain, or stone in the bladder and urethra causing symptoms * Current or a history within 5 years of lower urologic malignancies (e.g., bladder cancer), lower urinary tract surgery, previous pelvic irradiation, or severe neurological disease affecting bladder function or muscle strength (e.g., multiple sclerosis, Parkinson's disease, spinal cord injury, spina bifida) * Symptoms of severe stress urinary incontinence in the opinion of the investigator * Urinary retention or a post void residual volume in excess of 150 mL as confirmed by bladder ultrasound performed after suspicion of urinary retention * Habitual or psychogenic polydipsia (fluid intake resulting in a urine production exceeding 40 mL/kg/24 hours) or a mean volume voided per void of 350 mL or more during one or more 24-hour periods as assessed by the screening diaries * Central or nephrogenic diabetes insipidus * Syndrome of inappropriate antidiuretic hormone (SIADH) * Gastric retention * Myasthenia gravis * Uncontrolled narrow-angle glaucoma * Suspicion or evidence of cardiac failure * Uncontrolled and clinically relevant (in the judgement of the investigator) hypertension or diabetes mellitus * History and/or current treatment of obstructive sleep apnoea * Hyponatraemia:Serum sodium level must not be below 135 mmol/L * Evidence of potential renal impairment:Serum creatinine must be within normal laboratory reference intervals AND estimated glomerular filtration rate must be more than or equal to 50 mL/min * Hepatic and/or biliary diseases: Aspartate aminotransferase and/or alanine aminotransferase levels must not be more than twice the upper limit of normal range. Total bilirubin level must not be more than 1.5 mg/dL * Pregnancy, breastfeeding, or a plan to become pregnant during the period of the trial. Women of reproductive age must have documentation of a reliable method of contraception. All pre- and perimenopausal women have to perform pregnancy tests. Amenorrhea of more than 12 months duration based on the reported date of the last menstrual period is sufficient documentation of post-menopausal status and does not require a pregnancy test * Known alcohol or substance abuse; work or lifestyle that may interfere with regular night-time sleep e.g., shift workers; or any other medical condition, laboratory abnormality, psychiatric condition, mental incapacity, illiteracy or language barrier which, in the judgement of the investigator, would impair participation in the trial * Known or suspected hypersensitivity to any active ingredient or excipients in the investigational medicinal products used in the trial * Previous participation in any desmopressin trial within the last 5 years * Use of any prohibited therapy, as defined in the protocol

Study locations

24 registered sites.

United States. Showing up to 24 locations stored in the fast local snapshot.

NEA Baptist Clinic

Jonesboro, Arkansas, United States

Lynn Institute of The Ozarks

Little Rock, Arkansas, United States

Moez Khorsandi, DO

Los Angeles, California, United States

Urology Group of Southern California

Los Angeles, California, United States

Riverside Clinical Research

Edgewater, Florida, United States

Health Awareness, Inc.

Jupiter, Florida, United States

Pines Clinical Research, Inc.

Pembroke Pines, Florida, United States

Palm Beach Research Center

West Palm Beach, Florida, United States

Clinical Research Atlanta

Stockbridge, Georgia, United States

Northshore Center for Gastroenterology

Evanston, Illinois, United States

Remedica, LLC

Rochester, Michigan, United States

The Urological Institute of Northeastern New York

Albany, New York, United States

Premier Medical Group of the Hudson Valley, P.C.

Poughkeepsie, New York, United States

Parkhurst Research Organization, LLC

Bethany, Oklahoma, United States

Philadelphia Clinical Research, LLC

Philadelphia, Pennsylvania, United States

Medical University of South Carolina

Charleston, South Carolina, United States

Coastal Carolina Research Center

Mt. Pleasant, South Carolina, United States

Vanderbilt University Medical Center

Nashville, Tennessee, United States

Research Across America

Dallas, Texas, United States

Advances in Health

Houston, Texas, United States

Pioneer Research Solutions, Inc.

Houston, Texas, United States

Radiant Research

San Antonio, Texas, United States

Clinical Research Associates of Tidewater

Norfolk, Virginia, United States

Seattle Women's: Health, Research, Gynecology

Seattle, Washington, United States

Publications

Results and literature.

No PMID-linked publications were present in this registry snapshot.

Primary links

Continue at the source.

Related trials

More studies on Desmopressin.

Related PeptideStat pages

Put the record in context.

Research pages describe evidence. Vendor pages, where available, describe independently tracked research-product listings and are not clinical recommendations.