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Clinical Study of Solifenacin Succinate in Patients With Bladder Symptoms Due to Spinal Cord Injury or Multiple Sclerosis (SONIC)

This study has been completed.
Sponsor:
ClinicalTrials.gov Identifier:
NCT00629642
First Posted: March 6, 2008
Last Update Posted: September 1, 2017
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Information provided by (Responsible Party):
Astellas Pharma Inc
February 26, 2008
March 6, 2008
September 1, 2017
March 14, 2008
January 28, 2011   (Final data collection date for primary outcome measure)
Change from baseline in maximum cystometric capacity [ Time Frame: 4 Weeks ]
Same as current
Complete list of historical versions of study NCT00629642 on ClinicalTrials.gov Archive Site
  • Change from baseline in bladder volume at first involuntary contraction [ Time Frame: 4 Weeks ]
  • Change from baseline in pressure at first leak [ Time Frame: 4 Weeks ]
  • Change from baseline in volume at first leak [ Time Frame: 4 Weeks ]
  • Change from baseline in maximum detrusor pressure [ Time Frame: 4 Weeks ]
  • Change from baseline in micturition or catheterization frequency [ Time Frame: 4 Weeks ]
  • Change from baseline in incontinence episodes [ Time Frame: 4 Weeks ]
  • Incidence and severity of adverse events [ Time Frame: 4 Weeks ]
Same as current
Not Provided
Not Provided
 
Clinical Study of Solifenacin Succinate in Patients With Bladder Symptoms Due to Spinal Cord Injury or Multiple Sclerosis
A Randomized, Double Blind, Double Dummy, Placebo Controlled Study to Evaluate the Efficacy and Safety of Solifenacin Succinate (5 and 10mg Once Daily) Against Placebo and Oxybutynin Hydrochloride (5 mg Three Times Daily) in the Treatment of Subjects With Neurogenic Detrusor Overactivity
A clinical study to evaluate the efficacy and safety of solifenacin in patients with bladder symptoms due to spinal cord injury or multiple sclerosis
A clinical study to compare the efficacy and safety of solifenacin succinate in patients with neurogenic detrusor overactivity. In this randomized, double blind, double dummy study solifenacin will be compared to placebo and an active comparator, oxybutynin hydrochloride. Patients will be randomized to one of four treatment arms; solifenacin 10mg, solifenacin 5mg, placebo or oxybutynin 15mg. Patients will be assessed over a four week treatment period.
Interventional
Phase 4
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
Primary Purpose: Treatment
  • Multiple Sclerosis
  • Neurogenic Bladder
  • Spinal Cord Diseases
  • Drug: Solifenacin Succinate
    Oral, 10mg
    Other Names:
    • Vesicare
    • YM905
  • Drug: Solifenacin Succinate
    Oral, 5mg
    Other Names:
    • Vesicare
    • YM905
  • Drug: Oxybutynin Hydrochloride
    Oral, 15mg
  • Drug: Placebo
    Oral
  • Experimental: I.Solifenacin succinate 10mg (2x5mg 1/day)
    Oral
    Intervention: Drug: Solifenacin Succinate
  • Experimental: II.Solifenacin succinate 5mg (5mg 1/day)
    Oral
    Intervention: Drug: Solifenacin Succinate
  • Active Comparator: III.Oxybutynin hydrochloride 15mg (5mg 3/day)
    Oral
    Intervention: Drug: Oxybutynin Hydrochloride
  • Placebo Comparator: IV. Placebo
    Oral
    Intervention: Drug: Placebo
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Completed
249
January 28, 2011
January 28, 2011   (Final data collection date for primary outcome measure)

Inclusion Criteria:

  • Written informed consent has been obtained
  • Subjects with neurogenic detrusor overactivity due to:

    • Multiple sclerosis(MS)(EDSS≤8) or
    • Spinal cord injury(SCI)(partial or complete lesions)
  • MS or SCI symptoms should be stable for >= 6 months
  • Neurogenic detrusor overactivity symptoms should be stable for >= 6 months
  • Subject is willing and able to perform clean, intermittent, catheterization, if required
  • Subject is willing and able to take study medication in compliance with the protocol

Exclusion Criteria:

  • Subjects with neurogenic detrusor overactivity due to Parkinson's or cerebrovascular disease
  • Subjects with Sjögren's Syndrome or any similar symptoms
  • Subjects with evidence of a symptomatic urinary tract infection, chronic inflammation such as interstitial cystitis, bladder stones, previous pelvic radiation therapy or previous or current malignant disease of the pelvic organs
  • Subjects with stress incontinence or mixed incontinence where stress is the predominant factor as determined by the investigator
  • Subjects with evidence of pressure sores >= grade 2
  • Subjects with a history of bladder sphincterotomy
  • Subjects with known history of vesico-ureteral reflux without upper urinary tract infection
  • Any clinically significant condition, which in the opinion of the investigator makes the subject unsuitable for the study or includes a history of acute urinary retention, severe gastrointestinal obstruction (including paralytic ileus or intestinal atony), severe gastrointestinal conditions (including toxic megacolon or ulcerative colitis), myasthenia gravis, narrow angle glaucoma or shallow anterior chamber
  • Subjects undergoing hemodialysis
  • Subjects with severe hepatic impairment
  • Concurrent use of drugs intended to treat symptoms of overactive bladder
  • Use of antidepressants or muscle relaxants which have not been administered at a constant dose for >= 3 months
  • Use of non-drug treatment intended to treat overactive bladder symptoms including electrostimulation therapy, botulinum toxin and vanilloids therapy in the six months prior to the commencement of the study
  • Use of permanent, indwelling catheters
  • Known or suspected hypersensitivity to solifenacin succinate, oxybutynin hydrochloride, other anti cholinergics or lactose
  • Concomitant use of a strong CYP3A4 inhibitor, e.g. ketoconazole
  • Pregnant women, women who intend to become pregnant during the study, women of childbearing potential who are sexually active and practicing an unreliable method of birth control or women who will be lactating during the study. Reliable contraceptive methods are intra-uterine devices, contraceptive pills of combination type, hormonal implants and injectable contraceptives
  • Participation in any clinical study within 30 days of randomization, or the limit set by national law, whichever is longer
  • Employees of the Astellas Group, third parties associated with the study, or the study site
  • Subjects with maximum bladder capacity >= 400ml at visit 2
Sexes Eligible for Study: All
18 Years to 65 Years   (Adult)
No
Contact information is only displayed when the study is recruiting subjects
Australia,   Belgium,   Czechia,   France,   Germany,   Hungary,   Italy,   Netherlands,   Russian Federation,   Spain,   United Kingdom
Czech Republic,   Portugal
 
NCT00629642
905-EC-005
2006-005523-42 ( Other Identifier: EudraCT )
No
Not Provided
Plan to Share IPD: Yes
Plan Description: Details of the IPD sharing plan for this study can be found at www.clinicalstudydatarequest.com.
URL: http://
Astellas Pharma Inc
Astellas Pharma Inc
Not Provided
Principal Investigator: Department of (Neuro) Urology Universitaire Ziekenhuizen Leuven
Astellas Pharma Inc
August 2017

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP