Urinary Nerve Growth Factor (NGF), Prostaglandin E2 (PGE2)and Adenosine Triphosphate (ATP): Potential Biomarkers in Overactive Bladder Patients
NCT01499069 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 191
Last updated 2019-12-02
Summary
Nerve growth factor (NGF), prostaglandin E2 (PGE2)and adenosine triphosphate (ATP) levels in urine were reported to increase in patients with overactive bladder (OAB). Also, administration of the anti-muscarinic agent was reported to decrease urinary NGF and ATP.
The investigators aimed to explore the value of the urinary NGF, PGE2 and ATP as biomarker for predicting the treatment responsiveness and symptom relapse in OAB patients. So, the patients can be categorized into responder or non- responder and relapse or non-relapse groups. Ultimately, they can receive individualized treatments.
Conditions
Interventions
- DRUG
-
Oxybutinin, Fesoterodine, Solifenacin, Propiverin, Trospium
Dosage and frequency can be adjusted according to the patients' symptoms based on the instruction for administration . Duration; 3 or 6 months
Sponsors & Collaborators
-
Samsung Biomedical Research Institute
collaborator UNKNOWN -
Samsung Medical Center
lead OTHER
Principal Investigators
-
Kyu-Sung Lee, Ph.D · Samsung Medical Center
Study Design
- Allocation
- NA
- Purpose
- OTHER
- Masking
- NONE
- Model
- SINGLE_GROUP
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2010-02-28
- Primary Completion
- 2015-11-30
- Completion
- 2016-02-29
Countries
- South Korea
Study Locations
More Related Trials
-
Comparative Effectiveness of Initial OAB Treatment Options Among Older Women at High Risk of Falls
NCT05880862 ·Status: ACTIVE_NOT_RECRUITING ·Phase: EARLY_PHASE1
-
The Efficacy of Pyridostigmine Therapy After Transurethral Resection of Prostate in Cases with Underactive Urinary Bladder.
NCT06753071 ·Status: COMPLETED ·Phase: PHASE4
-
Effect of beta3-adrenoceptor Agonist on Patients With Overactive Bladder and as a Urinary Biomarker
NCT04693897 ·Status: UNKNOWN
-
Urinary Urgency Outcomes Following Propiverine Treatment for an Overactive Bladder
NCT00903045 ·Status: COMPLETED ·Phase: PHASE4
-
Sugammadex v.s. Neostigmine/Glycopyrrolate
NCT06398899 ·Status: COMPLETED ·Phase: NA
-
Efficacy, Tolerability and Impact on Quality of Life of Propiverine in Patients With Overactive Bladder Syndrome
NCT02024945 ·Status: COMPLETED
-
Assessment of Patient-reported Goal Attainment in the Treatment of Female Overactive Bladder
NCT00836381 ·Status: COMPLETED ·Phase: PHASE4
-
Effect of Mirabegron on Bladder Compliance
NCT05745584 ·Status: UNKNOWN ·Phase: NA
-
Comparisons of the Impact of Monotherapy With Mirabegron or Tolterodine Versus Combined Treatment With Mirabegron and Tolterodine on Autonomic Function and Bladder Blow Flow in Women With Overactive Bladder Syndrome: a Randomized Controlled Study
NCT05946902 ·Status: UNKNOWN ·Phase: PHASE4
-
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
-
Comparison of Caffeine Reduction and Anticholinergic Medications for Treatment of Overactive Bladder
NCT00780832 ·Status: TERMINATED ·Phase: NA
-
Comparative Urine Proteomic Studies of Overactive Bladder in Humans
NCT01367886 ·Status: COMPLETED ·Phase: NA
-
Mirabegron, Propevirine, Solifenacin for Treatment of Lower Urinary Tract Symptoms During Intravesical BCG Instillation
NCT05490082 ·Status: UNKNOWN ·Phase: PHASE3
-
Mirabegron for the Treatment of Pain Motivated Urinary Frequency and Urgency in Women
NCT02981459 ·Status: WITHDRAWN ·Phase: PHASE4
-
Therapeutic Efficacy and Safety of Mirabegron Treatment on Patients With Overactive Bladder Syndrome in Taiwan
NCT03044912 ·Status: UNKNOWN ·Phase: PHASE3
-
Investigation of Tolterodine, Pregabalin and a Tolterodine - Pregabalin Combination for the Treatment of Overactive Bladder
NCT00746681 ·Status: COMPLETED ·Phase: PHASE2
-
Predictors Affecting Long-term Use of Solifenacin or Mirabegron in Women With Overactive Bladder Syndrome
NCT05040984 ·Status: UNKNOWN
-
A Prospective, Observational, Multicenter Study of Patients Following Initiation of a New Course of Treatment for Overactive Bladder (OAB)
NCT02386072 ·Status: COMPLETED
-
Safety and Efficacy Study of AGN-214868 in Patients With Idiopathic Overactive Bladder and Urinary Incontinence
NCT01157377 ·Status: COMPLETED ·Phase: PHASE2
-
Treatment Persistence Among Patients With Overactive Bladder: A Retrospective Secondary Data Analysis in Asia Oceania
NCT03602508 ·Status: COMPLETED
-
A Study of the Efficacy and Safety of Vibegron (MK-4618) in Participants With Overactive Bladder (OAB) (MK-4618-008)
NCT01314872 ·Status: COMPLETED ·Phase: PHASE2
-
Investigation of Brain Mechanisms Involved in Urgency Urinary Incontinence
NCT04227184 ·Status: COMPLETED ·Phase: PHASE4
-
The Effect of Nighttime Mirabegron, Solifenacin, Tolterodine, or Oxybutynin on Nocturia, Sexual Function, Autonomic Function, and Lower Urinary Tract Blood Flow Perfusion in Women With Overactive Bladder Syndrome: Randomized Controlled Trial
NCT07114640 ·Status: NOT_YET_RECRUITING ·Phase: PHASE3
-
SMP-986 Phase 2 Proof of Concept in Patients With Overactive Bladder Syndrome (OABS)
NCT00409539 ·Status: COMPLETED ·Phase: PHASE2
-
Examining the Effects of Intra-detrusor Botox at Time of HoLEP in Men With Overactive Bladder Symptoms
NCT05878951 ·Status: RECRUITING ·Phase: PHASE2/PHASE3