Mapping of the Human Brainstem During Continence and Micturition: Noninvasive 7-T fMRI Study

Sponsor
The Methodist Hospital Research Institute (Other)
Overall Status
Active, not recruiting
CT.gov ID
NCT04846387
Collaborator
(none)
20
1
23.4
0.9

Study Details

Study Description

Brief Summary

The lower urinary tract (bladder, bladder neck, urethra and urethral sphincter) has two functions: Storage (Continence) and voiding (micturition). Lower urinary tract dysfunction (LUTD) includes symptoms in the storage phase (such as urinary frequency, urgency, incontinence) or micturition phase (such as voiding dysfunction, hesitancy and urinary retention), or both. Proper urinary tract function is controlled by a complex network of peripheral and central nervous system. A delicate and complex switch exists between storage of urine and elimination of urine and in humans, the control over this switch is located in brain stem. Although significant research efforts have been utilized to understand supraspinal neural control of LUTs in humans, our understanding of the brainstem in humans is very limited, mainly due to the small size of nuclei.

The extensive involvement of the brainstem in LUTS control has urged us to look into a better way to investigate and identify the brainstem nuclei involved throughout the entire bladder cycle, especially in neurogenic patients. To our knowledge, there has been no published study using high-resolution MRI (7 Tesla) to study the role of brainstem specifically in LUT. Brainstem evaluation in regards to LUT function in a thorough and accurate manner using high-resolution techniques is of high priority for benign urology and National Institute of Health. The findings from this proposal will lay the foundation to study of brainstem control in the bladder cycle in neurogenic patients with high-resolution neuroimaging, and will be seminal research in the field.

The investigators hypothesize that Grey matter (blood-oxygen-level-dependent BOLD) signals and functional connectivity (FC) evaluation of the brainstem regions involved in continence and micturition are superior in 7T when compared to 3T in humans allowing assessment of the variations between men and women. Brainstem Regions of Interest (ROIs) include Pontine Storage Center (PSC) ("L region of the pons) and PAG are expected to be activated during the storage (continence) phase and Pontine Micturition Center (PMC) ("M" region of the pons) are expected to be activated during the voiding (micturition) phase.

Condition or Disease Intervention/Treatment Phase
  • Diagnostic Test: Magnetic Resonance Imaging (MRI)
  • Diagnostic Test: Post-Void Residual
  • Diagnostic Test: Uroflowmetry
  • Behavioral: Questionaire - AUA Symptom Score

Detailed Description

The current proposal will be the first 7-Tesla study evaluating brain and specifically brainstem control over LUT. The study will utilize a noninvasive functional MRI (fMRI) protocol that allows for evaluation of brainstem activity during continence and micturition in real-time, using high-resolution neuroimaging techniques (7T fMRI) in both men and women. The study will recruit 20 healthy subjects (10 male and 10 female) for participation in this study. The participants for this study will undergo a few tests including a uroflow, PVR and a protocol training session during screening at visit 1, and a fMRI at visit 2.

During screening, subject will be asked to come to their appointment with a full bladder. For the uroflow, they will urinate into a special funnel connected to a measuring instrument in a private bathroom followed by measuring Post void residual volume through PVR scanner. This is to ensure that they do not have any urological issue which can disqualify them from the study. At this visit, we will also instruct them about the urine voiding-holding task, our noninvasive fMRI paradigm which will involve having the participant drink 500-750 mL of water approximately 20 minutes prior to the start of their scan, which the subjects will be performing during the fMRI portion of the study at visit 2.

The subsequent Grey matter (BOLD) signals and functional connectivity (FC) analysis will allow investigators to further the current understanding of brainstem control of the LUT and bladder cycle.

Study Design

Study Type:
Observational
Anticipated Enrollment :
20 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
High-resolution Mapping of the Human Brainstem During Continence and Micturition: in Vivo Noninvasive 7 Tesla fMRI Study
Actual Study Start Date :
Jan 18, 2021
Anticipated Primary Completion Date :
Dec 31, 2022
Anticipated Study Completion Date :
Dec 31, 2022

Arms and Interventions

Arm Intervention/Treatment
Females with Normal Bladder Function

Diagnostic Tests: functional MRI and urodynamic studies. During screening, subject will be asked to come to their appointment with a full bladder. For the uroflow, they will urinate into a special funnel connected to a measuring instrument in a private bathroom followed by measuring Post void residual volume through PVR scanner. This is to ensure that they do not have any urological issue which can disqualify them from the study. At this visit, we will also instruct them about the urine voiding-holding task, our noninvasive fMRI paradigm, which the subjects will be performing during the fMRI portion of the study at visit 2. A 7-Tesla Siemens MAGNETOM scanner will be used. A urinary pouch will be used to collect the participant's urine while in the scanner.

Diagnostic Test: Magnetic Resonance Imaging (MRI)
A T1-weighted Anatomical Image, Diffusion Weighted Image, and functional MRI (fMRI) of "empty bladder" image will be obtained. Additionally, fMRI image during "full bladder" state and voiding/holding tasks will be obtained.

Diagnostic Test: Post-Void Residual
The patient's post-void residual is determined using a portable ultrasound machine after emptying the bladder just prior to entering the MRI scanner and immediately after the MRI scan.
Other Names:
  • PVR
  • Diagnostic Test: Uroflowmetry
    Patients will urinate into a funnel connected to an electric flow meter to record urine flow rates in mililters per second. This is used as part of the screening process.

    Behavioral: Questionaire - AUA Symptom Score
    Subjects will fill out questionnaire asking about urinary symptoms. The range is 0-35.
    Other Names:
  • AUASS
  • Males with Normal Bladder Function

    Diagnostic Tests: functional MRI and urodynamic studies. During screening, subject will be asked to come to their appointment with a full bladder. For the uroflow, they will urinate into a special funnel connected to a measuring instrument in a private bathroom followed by measuring Post void residual volume through PVR scanner. This is to ensure that they do not have any urological issue which can disqualify them from the study. At this visit, we will also instruct them about the urine voiding-holding task, our noninvasive fMRI paradigm, which the subjects will be performing during the fMRI portion of the study at visit 2. A 7-Tesla Siemens MAGNETOM scanner will be used. A condom catheter will be used to collect the participant's urine while in the scanner.

    Diagnostic Test: Magnetic Resonance Imaging (MRI)
    A T1-weighted Anatomical Image, Diffusion Weighted Image, and functional MRI (fMRI) of "empty bladder" image will be obtained. Additionally, fMRI image during "full bladder" state and voiding/holding tasks will be obtained.

    Diagnostic Test: Post-Void Residual
    The patient's post-void residual is determined using a portable ultrasound machine after emptying the bladder just prior to entering the MRI scanner and immediately after the MRI scan.
    Other Names:
  • PVR
  • Diagnostic Test: Uroflowmetry
    Patients will urinate into a funnel connected to an electric flow meter to record urine flow rates in mililters per second. This is used as part of the screening process.

    Behavioral: Questionaire - AUA Symptom Score
    Subjects will fill out questionnaire asking about urinary symptoms. The range is 0-35.
    Other Names:
  • AUASS
  • Outcome Measures

    Primary Outcome Measures

    1. Blood Oxygen Level Dependent (BOLD) signals intensity [2 years]

      BOLD signal intensity in the regions of interest during empty bladder, full bladder, and micturition in healthy males and females

    Secondary Outcome Measures

    1. Blood Oxygen Level Dependent (BOLD) signals [2 years]

      Differences in BOLD signal intensity in brainstem ROIs during micturition between genders

    2. Uroflow measure [2 years]

      Maximum Qmax of urine (ml/sec): The range is between 0-40 mL/sec.

    3. Postvoid Residual [2 years]

      Postvoid Residual (PVR) of urine in mL: The range is between 0-900 mL.

    4. Urinary symptoms scores [2 years]

      Urinary symptom scores (no unit): The range is between 0-35. A higher score is associated with a worse outcome.

    5. Mean Diffusivity (MD) [2 years]

      MD is a scalar value that describes the degree of diffusivity. MD of white matter tracts that are implicated in brain control of bladder are of interest.

    6. Fractional Anisotropy (FA) [2 years]

      FA is a scalar value between zero and one that describes the degree of anisotropy of a diffusion process. A value of zero means that diffusion is isotropic (equally restricted) in all direction. No units. FA of white matter tracts that are implicated in brain control of bladder are of interest.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    Yes
    Inclusion Criteria:

    • Healthy adult male and female volunteers ≥18 years of age with no neurological disease and genitourinary abnormalities will be screened:

    • Post-Void Residual (PVR) < 20% of their bladder capacity OR

    • Above 10 percentile of Liverpool nomogram

    AND

    • AUASS score < 7 will be eligible to participate in the study.

    Exclusion Criteria:
    • history of clinically relevant genitourinary malignancy or surgery such as:

    • anti-incontinence procedures

    • urethral strictures

    • advanced pelvic organ prolapse

    • any neurological disorders

    • history of seizures,

    • pregnancy or planning to become pregnant,

    • and contraindications to MRI will be excluded.

    • Research team members who are involved with the data collection and the data analysis for this study.

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Houston Methodist Hospital Houston Texas United States 77030

    Sponsors and Collaborators

    • The Methodist Hospital Research Institute

    Investigators

    • Principal Investigator: Rose Khavari, MD, The Methodist Hospital Research Institute

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Rose Khavari, M.D., Principal Investigator, Houston Methodist Hospital Urologist and Research Director, The Methodist Hospital Research Institute
    ClinicalTrials.gov Identifier:
    NCT04846387
    Other Study ID Numbers:
    • PRO00026967
    First Posted:
    Apr 15, 2021
    Last Update Posted:
    Sep 13, 2021
    Last Verified:
    Sep 1, 2021
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Keywords provided by Rose Khavari, M.D., Principal Investigator, Houston Methodist Hospital Urologist and Research Director, The Methodist Hospital Research Institute

    Study Results

    No Results Posted as of Sep 13, 2021