"Swallow my Urine Back" : Inhibition of Detrusor Overactivity by Swallowing Maneuver
NCT01408771 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 20
Last updated 2011-08-09
Summary
The purpose of this study is to find out whether swallowing has an effect on the degree of urinary urgency and on the amplitude of detrusor contraction during filling cystometry in patients with detrusor overactivity (DO).
Conditions
- Overactive Detrusor
Sponsors & Collaborators
-
Assaf-Harofeh Medical Center
lead OTHER_GOV
Principal Investigators
-
Kobi Stav, MD · Assaf Harofeh Medical Center, Zeriffin, Israel
Eligibility
- Min Age
- 30 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2011-04-30
- Primary Completion
- 2011-07-31
- Completion
- 2011-07-31
More Related Trials
-
Observational Study to Estimate the Dry Mouth in OAB Patients With Solifenacin
NCT01437670 ·Status: COMPLETED
-
Post-treatment Novmalized Urodynamiz Findings as the Golden Standard of Objective Cure for Female Overactive Bladder Patients Receiving Antimuscarinic Drug
NCT01627145 ·Status: UNKNOWN ·Phase: NA
-
A Study Measuring and Tracking Changes in Overactive Bladder (OAB) Medication
NCT01317810 ·Status: WITHDRAWN
-
Effect of Long Acting Anticholinergic on Nocturnal Incontinence After Radical Cystectomy and Orthotopic Neobladder
NCT02877901 ·Status: COMPLETED ·Phase: PHASE2/PHASE3
-
Examining the Effects of Intra-detrusor Botox at Time of HoLEP in Men With Overactive Bladder Symptoms
NCT05878951 ·Status: RECRUITING ·Phase: PHASE2/PHASE3
-
A Pilot Trial in a Sleep Laboratory Setting to Observe Night Time Bladder Function of Subjects With Overactive Bladder (OAB)
NCT01099345 ·Status: TERMINATED
-
Evaluating a Digital Intervention for Overactive Bladder
NCT05170100 ·Status: COMPLETED ·Phase: NA
-
A Study to Evaluate the Efficacy of Tolterodine on Specific Symptoms in Adult Patients With Overactive Bladder.
NCT00645281 ·Status: COMPLETED ·Phase: PHASE4
-
A Multicenter VESIcare® Efficacy and Safety Study for the Treatment of Urgency Associated With Overactive Bladder (OAB)
NCT00454896 ·Status: COMPLETED ·Phase: PHASE3
-
Effect of Detrol LA on Overactive Bladder Symptoms, Sexual Quality of Life and Sexual Function in Women
NCT00143481 ·Status: COMPLETED ·Phase: PHASE4
-
Bladder Diary for Diagnosing Bladder Oversensitivity
NCT04981015 ·Status: COMPLETED
-
Validation of a Real-time Urodynamic Measure of Urinary Urgency
NCT00909428 ·Status: COMPLETED ·Phase: PHASE4
-
Study of Topically Administered Oxybutynin Gel in Patients With Urge Incontinence
NCT00909181 ·Status: COMPLETED ·Phase: PHASE3
-
Urodynamics and Clinical Factors That Are Associated With Bladder Over-sensitivity
NCT03486639 ·Status: UNKNOWN
-
Comparison of Caffeine Reduction and Anticholinergic Medications for Treatment of Overactive Bladder
NCT00780832 ·Status: TERMINATED ·Phase: NA
-
Study Evaluating the Safety, Tolerability, and Efficacy of Dexmecamylamine (TC-5214) for Treatment of Overactive Bladder
NCT01868516 ·Status: COMPLETED ·Phase: PHASE2
-
A Study to Assess the Long Term Effect, Safety and Metabolism of a Solifenacin Liquid Suspension in Participants 5 to 18 Years of Age With Neurogenic Detrusor Overactivity
NCT01565694 ·Status: COMPLETED ·Phase: PHASE3
-
URO-902 in Female Subjects With Overactive Bladder and Urge Urinary Incontinence
NCT04211831 ·Status: COMPLETED ·Phase: PHASE2
-
Effects of Antimuscarinic Drugs on Overactive Bladder (OAB) Symptoms After Insertion of Ureteral Stents
NCT01210859 ·Status: WITHDRAWN
-
A Therapeutic Exploratory Clinical Study of DA-8010 in Patients With Overactive Bladder
NCT03566134 ·Status: COMPLETED ·Phase: PHASE2
-
Age-specific Prevalence and Comparisons of UDS and Bladder Diary Between OAB-wet and -Dry Women
NCT03807024 ·Status: COMPLETED
-
Feasibility of "At-home" Titration of Solifenacin
NCT00759577 ·Status: TERMINATED ·Phase: PHASE4
-
AQUA: Anticholinergic Side Effects QUestionnAire
NCT04791111 ·Status: COMPLETED
-
Developing a Simple Test to Diagnose Overactive Bladder
NCT05572918 ·Status: UNKNOWN
-
A Two-week Open-label Pharmacodynamic and Pharmacokinetic Study of Multiple Doses of a Darifenacin Liquid Oral Suspension in Children (2 - 15 Years) With Neurogenic Detrusor Overactivity
NCT00712322 ·Status: TERMINATED ·Phase: PHASE2