EUCTR2012-004877-26-AT
Active, not recruiting
Phase 1
BOTOX® in the Treatment of Urinary Incontinence Due to Neurogenic Detrusor Overactivity in Patients 8 to 17 Years of Age
DrugsBOTOX®
Overview
- Phase
- Phase 1
- Intervention
- Not specified
- Conditions
- Not specified
- Sponsor
- Allergan Limited
- Enrollment
- 132
- Status
- Active, not recruiting
- Last Updated
- 7 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •1\. written informed consent has been obtained from the legally authorized representative and written minor assent has been obtained, in accordance with local laws and institutional review board (IRB)/independent ethics committee (IEC) requirements.
- •2\. written documentation has been obtained in accordance with the relevant country and local privacy requirements, where applicable (eg, Written Authorization for Use and Release of Health and Research Study Information (US sites) and written Data Protection consent (European sites).
- •3\. male or female, aged \= 8 years to \= 17 years of age at the time of informed consent.
- •4\. patient has NDO based on either:
- •\- presence of an IDC during the urodynamic assessment performed in the screening period or on day 1 (prior to randomization), or
- •\- documented presence of an IDC from an historical urodynamic assessment within 12 months of screening
- •5\. patient has NDO due to either:
- •\- spinal dysraphism, which includes spina bifida (eg, myelomeningocele, meningocele) and all forms of tethered cord ), or
- •\- acquired NDO from a spinal cord injury, with the injury having occurred at least 6 months prior to screening, or
- •\- acquired NDO due to transverse myelitis with diagnosis at least 18 monthsprior to screening
Exclusion Criteria
- •patient has an uncontrolled systemic disease, previous or current diagnosis of malignancy.
- •patient has had surgery of the spinal cord within 6 months of screening.
- •patient has a history or evidence of any pelvic or urological abnormalities, except NDO, including:
- •o bladder neck surgery resulting in an open bladder neck, or reconstructive surgery of the lower urinary tract (eg, urinary diversion, urostomy), except for the Mitrofanoff procedure, which is permitted.
- •o anatomical evidence of bladder outlet obstruction, urethral or urethral valve obstruction/stricture at screening
- •o surgery of the urinary tract including minimally invasive surgery (eg, bulking agents,
- •sling), within 6 months of screening (except those listed above which are exclusionary for any time period).
- •o circumcision within 1 month of screening
- •patient has cerebral palsy
- •patient has uncontrolled epilepsy, defined as:
Outcomes
Primary Outcomes
Not specified
Similar Trials
Completed
Phase 3
BOTOX® in the Treatment of Urinary Incontinence Due to Overactive Bladder in Patients 12 to 17 Years of AgeOveractive Bladderurinary incontinence10004994NL-OMON42096Allergan Limited15
Active, not recruiting
Phase 1
BOTOX® in the Treatment of Urinary Incontinence Due to Overactive Bladder in Patients 12 to 17 Years of AgeEUCTR2014-000464-17-GBAllergan Limited108
Active, not recruiting
Phase 1
BOTOX® in the Treatment of Urinary Incontinence Due to Overactive Bladder in Patients 12 to 17 Years of AgeEUCTR2014-000464-17-ITAllergan Limited108
Active, not recruiting
Phase 1
BOTOX® in the Treatment of Urinary Incontinence Due to Overactive Bladder in Patients 12 to 17 Years of Agerinary Incontinence Due to Overactive BladderMedDRA version: 18.0Level: PTClassification code 10046543Term: Urinary incontinenceSystem Organ Class: 10038359 - Renal and urinary disordersTherapeutic area: Not possible to specifyEUCTR2014-000464-17-FRAllergan Limited108
Active, not recruiting
Phase 1
BOTOX® in the Treatment of Urinary Incontinence Due to Overactive Bladder in Patients 12 to 17 Years of Agerinary Incontinence Due to Overactive BladderMedDRA version: 17.1Level: PTClassification code 10046543Term: Urinary incontinenceSystem Organ Class: 10038359 - Renal and urinary disordersTherapeutic area: Not possible to specifyEUCTR2014-000464-17-BEAllergan Limited108