Central Nervous System Changes Following BotulinumtoxinA Injection in the Bladder



Status:Recruiting
Conditions:Other Indications, Other Indications, Overactive Bladder, Neurology, Neurology, Multiple Sclerosis
Therapuetic Areas:Gastroenterology, Neurology, Other
Healthy:No
Age Range:18 - Any
Updated:4/17/2018
Start Date:February 2014
End Date:February 2019
Contact:Rashmi Pande, BDS, MS
Email:rpande@houstonmethodist.org
Phone:713-363-9154

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A Prospective Study of Higher Neural Control Changes Following Intradetrusor Injection of BotulinumtoxinA in Patients With Multiple Sclerosis and Lower Urinary Tract Symptoms.

The purpose of this prospective research study is to evaluate higher neural changes following
intradetrusor injection of Botulinum toxin-A (BTX-A) in patients with Multiple Sclerosis
(MS). Concurrent Urodynamic and Functional Magnetic Resonance (fMRI) data will be recorded
pre- and post- intravesical injection of BTX-A in patients with Multiple Sclerosis (MS) and
neurogenic detrusor activity (NDO).

Other objectives are to evaluate the role of urinary biomarkers such as brain-derived
neurotropic factor (BDNF) and nerve growth factor (NGF) associated with bladder overactivity
and, to determine whether the common validated urgency questionnaires correlate with fMRI
findings and urinary biomarker concentration pre- and post- BTX-A injection in patients with
MS and NDO.

Multiple Sclerosis is a severe debilitating disease that affects patient's quality of life.
Up to 90% of patients with MS will develop lower urinary tract dysfunction within the first
18 years of the disease. Lower urinary tract symptoms (LUTS) can range from urgency to urge
urinary incontinence and/or hesitancy and incomplete bladder emptying. Urgency, frequency,
and neurogenic detrusor overactivity (NDO) are the most common urologic findings (34-99%)
during diagnostic evaluations of patients with MS. Even though anticholinergic or beta
agonist drugs have limited effectiveness and adverse side effects, they are the first line
pharmacotherapy for patients with NDO if behavioral modifications and pelvic floor physical
therapy are unsuccessful. Botulinum toxin-A (BTX-A) intradetrusor injection is a highly
effective treatment option for patients with NDO who are refractory to more conservative
management. BTX-A blocks the release of acetylcholine at the neuromuscular junction and leads
to a temporary chemodenervation of the bladder (paralysis of the muscle). Motor effects of
BTX-A on the bladder have been extensively studied and widely reported in the literature, and
the US Food and Drug Administration has approved BTX-A for the treatment of detrusor
overactivity in neurogenic and non-neurogenic patients. However, the sensory effects of BTX-A
injection correlating to central nervous system regional perception/localization of urgency,
frequency, and urge incontinence in humans are not well known.

Over the past decades, functional MRI (fMRI) has been used to study the activation of
supraspinal lower urinary tract control centers in healthy subjects during the storage and
voiding phases. Given these facts, the investigators are interested in evaluating the role of
intradetrusor injection of BTX-A in afferent response in patients with MS and NDO.
High-resolution neuroimaging techniques will help investigators to further understand how MS
affects the bladder-brain controls. This study will use fMRI and task-related blood oxygen
level dependent (BOLD) signal to evaluate patients with MS and NDO prior to, and 6-10 weeks
after intradetrusor injection of BTX-A with simultaneous urodynamic evaluation.

Clinical correlation between women with these chronic urologic problems and new discoveries
at level of CNS activity will give a better understanding of this disorder, leading to the
development of more effective diagnostic and treatment modalities.

Inclusion Criteria:

- Patients with clinical diagnosis of neurogenic bladder.

- History of any neurologic illness or injury (including but not limited to spinal cord
injury, Multiple Sclerosis, spina bifida, Parkinson's, major spine surgery).

- 18 years or older.

- Female patients.

Exclusion Criteria:

- Male

- History of any incontinence surgery (sling, MMK, Burch).

- History of any lower urinary tract surgery or manipulation (urethral dilation).

- Positive urine pregnancy test at enrollment .
We found this trial at
1
site
6550 Fannin St
Houston, Texas 77030
(713) 790-3311
Principal Investigator: Rose Khavari, MD
Phone: 713-363-9154
Houston Methodist Hospital Houston Methodist is comprised of a leading academic medical center in the...
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