Overactive Bladder Clinical Trial
Official title:
Prospective Randomized Trial of Percutaneous Tibial Nerve Stimulation (PTNS) Versus PTNS and Fesoterodine Fumarate
The investigators are studying two FDA-approved modalities used to treat overactive bladder to determine if they improve overactive bladder with or without urge incontinence when used together rather than separately, percutaneous tibial nerve stimulation (PTNS) versus PTNS and fesoterodine fumarate.
Overactive bladder (OAB) is described as urinary urgency with or without urge incontinence,
usually associated with urinary frequency and nocturia. The primary complaint is a strong
desire to void without the ability to postpone micturition. Two treatments used in the
treatment of OAB are pharmacotherapy and percutaneous tibial nerve stimulation (PTNS).
Pharmacotherapy for OAB is based on medications that block the muscarinic receptors of the
detrusor muscle. These particular receptors are not unique to the bladder, however, and
patients complain of bothersome side effects that are a result of systemic muscarinic
receptor blockade. Medications are successful for many patients but compliance is poor and
many patients discontinue the medications as a result of side effects, cost, and
insufficient symptom improvement.
Percutaneous tibial nerve stimulation (PTNS) is a newer treatment modality that provides
neuromodulation to the pelvic floor by stimulating the posterior tibial nerve. This nerve is
accessed with a fine needle electrode that is inserted in the medial portion of the ankle.
This area has long been recognized as having nerve projections to the sacral nerve plexus
and can modulate bladder activity. Several studies have clearly demonstrated the
effectiveness of neuromodulation to treat urge incontinence.
There have been studies comparing the efficacy of pharmacotherapy versus PTNS. In one study,
49% of subjects taking fesoterodine fumarate for urge incontinence reported an improvement
in symptoms of overactive bladder. In other studies, 79.5% of patients undergoing PTNS
reported improvement or cure. Although studies report similar improvement or cure between
the two treatment modalities, there is no evidence of the efficacy of using both PTNS and
pharmacotherapy concurrently. This study is aimed at proving synergy between the two
treatment modalities when used together in an effort to administer smaller doses of
anticholinergic agents, while obtaining comparable or improved urge incontinence.
;
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Crossover Assignment, Masking: Double Blind (Subject, Investigator), Primary Purpose: Treatment
Status | Clinical Trial | Phase | |
---|---|---|---|
Recruiting |
NCT04578899 -
"The Effectiveness of Transvertebral Magnetic Neuromodulation in Patients With Detrusor Overactivity"
|
N/A | |
Active, not recruiting |
NCT03556891 -
Pivotal Study of eCoin for Overactive Bladder With Urgency Urinary Incontinence
|
N/A | |
Not yet recruiting |
NCT05977634 -
Transcutaneous Tibial Nerve Stimulation for Idiopathic Overactive Bladder
|
N/A | |
Completed |
NCT01955408 -
Severity of Overactive Bladder Symptoms in Patients After Synergo Treatment
|
N/A | |
Recruiting |
NCT06201013 -
Efficacy and Safety of Vitamin D in the Treatment of OAB-wet in Children
|
N/A | |
Recruiting |
NCT03727711 -
TPTNS: Home vs Hospital Treatment for Overactive Bladder
|
N/A | |
Completed |
NCT00768521 -
A Study to Test the Effects of Tolterodine Tartrate in Patients With Overactive Bladder (0000-107)
|
Phase 1 | |
Completed |
NCT03625843 -
Mindfulness Exercises to Reduce Anxiety and Pain During Urodynamic Testing
|
N/A | |
Completed |
NCT02211846 -
A Study to Evaluate the Pharmacokinetics, Safety and Tolerability of Mirabegron OCAS (Oral Controlled Absorption System) in Pediatric Subjects With Neurogenic Detrusor Overactivity or Overactive Bladder
|
Phase 1 | |
Completed |
NCT02857816 -
PRospective Study to Evaluate EffectivenesS With the NURO™ PErcutaneous Tibial Neuromodulation System in Patients With OAB
|
N/A | |
Completed |
NCT02835846 -
Investigation of the Effect of the Female Urinary Microbiome on Incontinence
|
Phase 4 | |
Withdrawn |
NCT02320201 -
Foot Neuromodulation for Overactive Bladder in Children
|
N/A | |
Completed |
NCT02202031 -
Controlling Urgency Through Relaxation Exercises
|
N/A | |
Not yet recruiting |
NCT01423838 -
Comparison of Solifenacin and Oxybutynin in the Treatment of Overactive Bladder
|
Phase 4 | |
Not yet recruiting |
NCT01409512 -
Evaluation of Autonomic System Before and After Anticholinergic Treatment in Women With Overactive Bladder
|
N/A | |
Completed |
NCT01437670 -
Observational Study to Estimate the Dry Mouth in OAB Patients With Solifenacin
|
N/A | |
Completed |
NCT01458197 -
A Phase 2 Study to Compare the Efficacy and Tolerability of Tarafenacin 0.2 mg and Tarafenacin 0.4 mg to Placebo in Patients Suffering From Overactive Bladder.
|
Phase 2 | |
Terminated |
NCT01758848 -
Physical Therapy for Overactive Bladder
|
N/A | |
Withdrawn |
NCT01210859 -
Effects of Antimuscarinic Drugs on Overactive Bladder (OAB) Symptoms After Insertion of Ureteral Stents
|
N/A | |
Completed |
NCT02667470 -
Reproducibility Study of OABSS and Its Response to Treatment
|
Phase 4 |