Solifenacin Succinate (VESIcare) for the Treatment of Overactive Bladder in Parkinson's Disease (URGE-PD)
This study is currently recruiting participants.
Verified March 2012 by University of South Florida
Sponsor:
University of South Florida
Collaborator:
Astellas Pharma Inc
Information provided by (Responsible Party):
Theresa Zesiewicz, University of South Florida
ClinicalTrials.gov Identifier:
NCT01018264
First received: November 19, 2009
Last updated: March 26, 2012
Last verified: March 2012
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Purpose
This study will assess the effectiveness of solifenacin succinate (VESIcare) in reducing symptoms of overactive bladder in Parkinson's disease (PD) patients.
| Condition | Intervention | Phase |
|---|---|---|
|
Overactive Bladder in Parkinson's Disease |
Drug: solifenacin succinate (VESIcare) Drug: placebo |
Phase 4 |
| Study Type: | Interventional |
| Study Design: | Allocation: Randomized Endpoint Classification: Efficacy Study Intervention Model: Parallel Assignment Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor) Primary Purpose: Treatment |
| Official Title: | URGE-PD: A Multi-site, Double-blind, Randomized, Placebo Controlled Trial of Solifenacin Succinate (VESIcare) for the Treatment of Overactive Bladder in Parkinson's Disease |
Resource links provided by NLM:
Further study details as provided by University of South Florida:
Primary Outcome Measures:
- The primary objective of this study is to measure the efficacy of solifenacin succinate (VESIcare) in reducing the mean number of micturitions per 24 hour period in Parkinson's disease (PD) patients as measured by voiding diaries. [ Time Frame: 12 weeks ] [ Designated as safety issue: No ]
Secondary Outcome Measures:
- To examine the effect of solifenacin succinate (VESIcare) on urinary incontinence severity [ Time Frame: 12 weeks ] [ Designated as safety issue: No ]
- To examine the effect of solifenacin succinate (VESIcare) on Parkinson's disease severity [ Time Frame: 12 weeks ] [ Designated as safety issue: No ]
- To examine the effect of solifenacin succinate (VESIcare) on quality of life [ Time Frame: 12 weeks ] [ Designated as safety issue: No ]
| Estimated Enrollment: | 30 |
| Study Start Date: | January 2010 |
| Estimated Study Completion Date: | March 2013 |
| Estimated Primary Completion Date: | March 2013 (Final data collection date for primary outcome measure) |
| Arms | Assigned Interventions |
|---|---|
| Experimental: solifenacin succinate (VESIcare) |
Drug: solifenacin succinate (VESIcare)
up to 10mg every day orally
|
| Placebo Comparator: placebo |
Drug: placebo
placebo matching solifenacin succinate (VESIcare) up to 10mg orally every day
|
Eligibility| Ages Eligible for Study: | 40 Years to 80 Years |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Criteria
Inclusion Criteria:
- Outpatients with idiopathic PD according to the UK Parkinson's Disease Society Brain Bank Clinical Diagnosis Criteria.
- Age 40 years to 80 years.
- Stable dose of antiparkinsonian medication 4 weeks prior to study entry.
- Patients must score 1.0 to 3.0 on the Modified Hoehn and Yahr scale.
- Women of child-bearing potential must use a reliable method of contraception.
- Must be experiencing symptoms of overactive bladder according to the ICS definition of a minimum voiding 8 or more times/24 hours and a daily average of at least 1 episode of urgency and/or urinary incontinence (urge incontinence predominately as measured by 3IQ diary) per 24 hours during a 3-day micturition diary period. Patients must have documentation of OAB within the last 6 months.
- The patient must have evidence of PSA less than or equal to 4 (males only) within the last 12 months (obtained from primary care physician).
- The patient must have had a bladder scan within six months of the screening visit. This scan uses ultrasound technology to measure residual fluid levels in the bladder after urination. This scan must document post void residual of 200 mls or less. A bladder scan printout or a note documenting these findings must be provided before baseline.
- Clearance from the patient's internist or primary care health provider who has examined the patient within the last 6 months.
Exclusion Criteria:
- Any illness that in the investigator's opinion preclude participation in this study.
- Pregnancy or lactation.
- Concurrent participation in another clinical study.
- Dementia or other psychiatric illness that prevents the patient from giving informed consent (Mini Mental Status Exam scores less than 27).
- Legal incapacity or limited legal capacity.
- History of prostate cancer or Transurethral resection of the prostate (TURP) (males only).
- Presence of severe renal disease. BUN 50% greater than normal (normal BUN levels should be within a range of 5 to 20 mg/ d L and creatinine between .7 and 1.4 mg/ d L). Labs within the past 12 months will be requested from the patient's health care provider or urologist. If labs are not available within this time-frame or if results are abnormal, labs will be obtained as part of the screening visit.
- Presence of major hepatic impairment (cirrhosis, viral hepatitis, nonalcoholic steatohepatitis, Wilson's disease, or Hemochromotosis).
- Currently taking ketaconazole (anti-fungal) or any CYP3A4 inhibitor such as itraconazole, ritonavir, nelfinavir, clarithromycin, or nefazadone.
- Any history of bladder outflow obstruction or gastrointestinal obstructive disorders.
- History of narrow angle glaucoma.
- Patients who have undergone pelvic radiation at any time.
Currently taking any of the following medications:
- Antiarrhythmics: flecainide (Almarytm, Apocard, Ecrinal, Flécaine), digoxin (Lanoxin, Digitek, Lanoxicaps)
- Antipsychotics: thioridazine (Mellaril, Novorizadine, Thioril)
- Tricyclic anti-depressants: amitriptyline (Elavil, Tryptanol, Endep, Elatrol, Tryptizol, Trepiline, Laroxyl), amoxapine (Asendin, Asendis, Defanyl, Demolox, Moxadil), clomipramine (Anafranil), desipramine (Norpramin, Pertofrane), imipramine (Antideprin, Deprenil, Deprimin, Deprinol, Depsonil, Dynaprin, Eupramin, Imipramil, Irmin, Janimine, Melipramin, Surplix, Tofranil), nortriptyline (Aventyl, Pamelor, Nortrilen), protriptyline (Vivactil), trimipramine (Stangyl, Surmontil, Rhotrimine)
- Psychotropics: doxepin (Aponal, Adapine, Sinquan, Sinequan)
- Anticholinergics/Antispasmodics: trihexyphenidyl (Artane, Aparkan), benztropine (Cogentin), oxybutynin (Ditropan, Ditropan XL, Lyrinel XL, Oxytrol), darifenacin (Enablex), emepronium, flavoxate (Urispas), meladrazine, propiverine, solifenacin (Vesicare), tolterodine (Detrol, Detrol LA), trospium (Sanctura)
- Selective Serotonin-Norepinephrine Reuptake Inhibitors (SNRI): duloxetine (Cymbalta, Yentreve), Venlafaxine (Effexor, Effexor XR)
- Arylalkylamines: pseudoephedrine (Sudafed)
- Anti-androgen: bicalutamide (Casodex, Cosudex, Calutide, Kalumid), finasteride (Proscar, Propecia, Fincar, Finpecia, Finax, Finast, Finara, Finalo, Prosteride, Gefina, Finasterid IVAX), dutasteride (Avodart, Avidart, Avolve, Duagen, Dutas, Dutagen, Duprost), Zoladex (goserelin acetate), Eulexin (flutamide), Lupron (leuprolide acetate)
- Antihypertensives: prazosin (Minipress, Vasoflex, Hypovase)
- Estrogens (Menest, Premarin, Premarin IV)
- Acetylcholinesterase inhibitors (rivastigmine (Exelon), galantamine, (Reminyl, donepezil (Aricept), Tacrine.
- Memantine (Namenda)
- Urinary obstruction in male PD patients as diagnosed by a urologist
- Active urinary tract infection.
- Patients with a history of chronic severe constipation (by self report)
Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT01018264
Contacts
| Contact: Kelly Sullivan, MSPH | 813-974-5909 | kbarber@health.usf.edu |
Locations
| United States, Florida | |
| University of Miami | Recruiting |
| Miami, Florida, United States, 33136 | |
| Contact: Wendy Levy, CCRC 305-243-3530 WLevy@med.miami.edu | |
| Principal Investigator: Carlos Singer, MD | |
| University of South Florida | Recruiting |
| Tampa, Florida, United States, 33612 | |
| Contact: Kelly Sullivan, MSPH 813-974-5909 kbarber@health.usf.edu | |
| Principal Investigator: Theresa Zesiewicz, MD | |
| United States, Georgia | |
| Emory University | Recruiting |
| Atlanta, Georgia, United States, 30329 | |
| Contact: Barbara Sommerfeld, MSN, RN 404-728-6944 bsommer@emory.edu | |
| Principal Investigator: Marian Evatt, MD | |
Sponsors and Collaborators
University of South Florida
Astellas Pharma Inc
Investigators
| Principal Investigator: | Theresa Zesiewicz, MD | University of South Florida |
| Principal Investigator: | Marian Evatt, MD | Emory University |
| Principal Investigator: | Carlos Singer, MD | University of Miami |
More Information
No publications provided
| Responsible Party: | Theresa Zesiewicz, Professor of Neurology, University of South Florida |
| ClinicalTrials.gov Identifier: | NCT01018264 History of Changes |
| Other Study ID Numbers: | Sullivan-9 |
| Study First Received: | November 19, 2009 |
| Last Updated: | March 26, 2012 |
| Health Authority: | United States: Institutional Review Board |
Keywords provided by University of South Florida:
|
Overactive bladder Urinary incontinence Urinary frequency Parkinson's disease |
Additional relevant MeSH terms:
|
Parkinson Disease Urinary Bladder, Overactive Parkinsonian Disorders Basal Ganglia Diseases Brain Diseases Central Nervous System Diseases Nervous System Diseases Movement Disorders Neurodegenerative Diseases Urinary Bladder Diseases Urologic Diseases |
Urological Manifestations Signs and Symptoms Quinuclidin-3'-yl-1-phenyl-1,2,3,4-tetrahydroisoquinoline-2-carboxylate monosuccinate Muscarinic Antagonists Cholinergic Antagonists Cholinergic Agents Neurotransmitter Agents Molecular Mechanisms of Pharmacological Action Pharmacologic Actions Physiological Effects of Drugs |
ClinicalTrials.gov processed this record on May 23, 2013