AzTrials
AzTrials

Urinary Incontinence, UrgeNCT04271852

An Experimental Protocol for the Study of Brain Functional Magnetic Resonance Imaging in Female With Urgent Urinary Incontinence

A study testing bio-feedback treatment in people with Urinary Incontinence, Urge, run by Second Affiliated Hospital of Wenzhou Medical University at 1 site in China.

Unknown status

Status not confirmed. The sponsor has not verified this record for over two years, so it may be out of date.

Official record
Search all trials

Trial summary

Background: Patients' life quality and physical and mental health are seriously affected by Urgent Urinary Incontinence(UUI). The cause is not clear at present. It has been found that the injury of the prefrontal lobe and damage to the surrounding cerebral cortex leads to significant lower urinary tract dysfunction. Read more about this study

Who is it for?
Ages 20 to 70 years, women onlyHealthy volunteers can take part
Conditions the study is for
Urinary Incontinence, Urge
What is being tested?
bio-feedback treatment
Type of treatment
Medical device
Could I receive a placebo?
No, everyone receives an active treatment
How many people
100 participants
Where
1 siteChina
Study dates
23 Oct 2019to 31 Dec 2022
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 20 to 70 years
  • Women only
  • Healthy volunteers accepted
  • Adult, Older adult

Who may be able to join

  • People in the group should meet the following inclusion criteria:
  • 20-70 years old, medical history ≥ 3 months.
  • According to International Continence Society, ICS, people in the group should be patients diagnosed with UUI.

Who cannot join

  • Exclusion standards should be met by both patient group and the control group ( Not included in if meeting one of the following items ):
  • Scan contraindication :(1)reactive metal.(2)cardiac pacemaker.(3)magnetic implantation.(3)no spring steel wire in eyelid.(4)artificial cochlea.(5)electrodes/wires, pregnancy, etc.
  • Patients with severe organ diseases :·(1)liver disease.(2)lung disease.(3)kidney disease.(4)Other diseases that may interfere with the effectiveness and safety assessment of the test or may place the patient at some particular risk.
  • People who is unable to cooperate with each other.
  • A neurological or other medical disease that affects the function of the central nervous system :(1) anemia.(2) vitamin B12 deficiency .(3)folic acid deficiency.
  • People who abuse drug.
Show all 15Show fewer
  • People who has dependence history
  • Hyperthyroidism in active period
  • cerebrovascular disease (e.g. transient ischemic attack, ischemic or hemorrhagic stroke, aneurysm)
  • Central nervous system infection
  • Alcoholic dementia
  • Uncontrolled epilepsy
  • Autoimmune disease
  • Diabetes mellitus
  • Detrusor hyperreflexia (cystitis, tuberculosis, tumor, stone, bladder outlet obstruction) and other organic lesion.

Trial locations and contacts

1 site in 1 country.

Ledan Wang, Doctor contact

13858850907

ledanwang331@163.com

Jiaorong Li, Master contact

19884692686

2026634592@qq.com

China1 site, 1 recruiting
  • Department of Gynecology of Second Affiliated Hospital of Wenzhou Medical University

    Wenzhou, Zhejiang, 325000

    Jiaorong Li, Master, +8619884692686, 2026634592@qq.com

    Recruiting

Other trials in China

About this study

Background: Patients' life quality and physical and mental health are seriously affected by Urgent Urinary Incontinence(UUI). The cause is not clear at present. It has been found that the injury of the prefrontal lobe and damage to the surrounding cerebral cortex leads to significant lower urinary tract dysfunction. Therefore, some scholars believe that urinary axis of the brain exist between the urinary system and the central nervous system, and the two are controlled by each other. Therefore, to study central conduction in patients with UUI and changes of physiology, pathology, brain chemical, brain structure in brain functional area caused by central sensitivity, in particular, changes in urine control cognition and midbrain limbic system (including memory function areas) in the brain, is beneficial to more in-depth understanding of its pathogenesis and treatment options. The Functional Magnetic Resonance Imaging provides a possibility for the study.

Method / design:Taking female UUI patients as target, through questionnaire survey, voiding diary, specialist physique, examination,ultrasonic examination of pelvic floor muscle, urodynamic examination and three sequence magnetic resonance scanning, after analyzing structural image of brian, resting functional images, dispersion tensor image, comparing with the normal control group and the female UUI group, before and after behavioral therapy in patients with UUI, and those who have no urinary incontinence and those who still have urinary incontinence after behavioral treatment, specific brain function biomarkers for female UUI patients are found and the brain function mechanism of the female UUI is to be explored in this project.

Discussion: This study breaks through the traditional limitations on the cause of incontinence.And it is the first time,the mental/behavior indicators of uui patients were combined with fMRI(Functional Magnetic Resonance Imaging) to explore biomarkers of brain and brain structural changes in patients .Then,it is becoming more and more important that the personalized treatment by building a UUI digital model using fMRI.

Read the detailed description

The study is a randomized controlled trial that study on the mechanism of brain function in women with urgent urinary incontinence by using fMRI. According to the exclusion criteria, 50 healthy volunteers and 50 UUI patients are recruited to carry out the related experimental research.This study had been approved by the Ethics Committee of the second affiliated Hospital of Wenzhou Medical University (No. LCK2019-291) .

1.50 UUI patients and 50 healthy volunteers who meet the inclusion criteria were selected.

(1) Approved by the Scientific Research Ethics Review Committee of the second affiliated Hospital of Wenzhou Medical University, 20- 70 years old female volunteers are recruited by studying advertising, reminding volunteers that the study is recruiting women with well bladder control function through the answer to the relevant questionnaires as a screening tool.

2.1 Healthy volunteers (n=50) should empty thier bladder first ;than they perform a fMRI scan.

2.2 The selected patients (n=50) will be inserted into 8F catheter for urine emptying, determination of bladder pressure and injection of aseptic water. First of all, the subjects empty their urine through the catheter, perform a fMRI scan first, and perform the following cycle module after the first scan is complete:①Paused for 11s ②.Injecting 22ml aquae sterilisata into bladder through catheter (completed in 11s ) ③.Paused for 11s ④.withdraw15ml liquid through catheter (completed in 11s ) , running 1-5 modules in circles until the subject issues a urination signal. With the subject's consent, the above cycle is repeated once, to exclude dropout who will be marked as a failure in the study. The rest of the patients completed the above circulation and patients with urine leakage scan the fMRI again.

3.Every fMRI scan of each subject included in the study will be scanned on GE-Discovery 7503T magnetic resonance machine for three sequences (T1,rsfMRI, DTI). The total scanning time is about 25 minutes. The brain structural image (T1) uses GE BRAVO sequence for about 5 minutes and the specific parameters are as follows:TR/TE=7.7/3.4 ms, Flip angle=12°, FOV=256 mm×256 mm, Resolution=256×256, Slice per volume=176, Slice thickness=1 mm. The rsfMRI(resting-state functional magnetic resonance) uses a single EPI sequence for about 10 minutes and the specific parameters are as follows.TR/TE=2000/30 ms, Flip angle=90°, FOV=220 mm×220 mm, Resolution=64×64, Slice thickness=4 mm, Slices per volume=32, Number of volumes=230. The diffusion tensor image (DTI) uses a single diffusion-weighted spin echo EPI sequence for about 10 minutes and the specific parameters are as follows:TR/TE=8000/80 ms, Flip angle=90°, FOV=256 mm×256 mm, Resolution=128×128, Slice thickness=2 mm, Slices per volume=75. In order to use the latest method to analyze the gray microstructure of the brain,investigators will choose two non-zero b values:b=1000 s/mm2 , with a total of 23 dispersion directions; b = 2000 s/mm2 , with a total of 49 dispersion directions.

  1. The 50 UUI patients who completed the above trial will be treated with behavioral therapy for 3 months under the guidance of medical staff. The behavioral therapy includes: (1) changes in the way of life including quit smoking, lose weight, keep a normal bowel movement, drinking water in a regular basis, no coffee and white spirit, don't eat spicy and irritating foods, regular urination and defecation, etc. (2) Bladder training: set a urination schedule, with a short interval of time at first, when feeling urination is urgent, the tension of bladder can be alleviated by slow deep breathing and mental transfer to increase the interval of urination gradually. (3) have pelvic floor muscle exercise by drawing up the anus such as, hold on to exhaust and defecate from the anus. The contraction lasts 3, 5 or 10 seconds. And then completely relax the anus. The relaxation time is equal to the drawing up time of anus with 10 to 15 times per exercise, and3 to 5 times a day.

5.Patients with UUI who completed 3 months' behavioral therapy repeat the above 2 -5 study steps again.

6.Relevant research parameters:Image parameters of brain function:investigators will first get the whole brain voxel image parameters and investigators get local gray matter density in structural image. Local degree will be gotten in functional image while local fractional anisotropy, FA will be gotten in the dispersion tensor image. Then by calculating global gray matter density, global degree and global FA, investigators will get the global variables of the brain function (structural, functional and white matter connection anisotropy) of the participants.

  1. Data analysis:①By comparing the image parameters of whole brain function with those of the normal control group (Student t-test group comparison, two tails, p < 0.05/3=0.017 (family-wise correction)),investigators will verify one of research assumptions, that is, whether the brain of the UUI patient has a significant change in function and structure (structural, functional, and white matter connection anisotropy) as compared to the brain of a normal person; At the same time, By comparing the image parameters of whole brain voxel image parameters with those of the normal control group (student t group comparison,two tails, p < 0.05, cluster size > 30 (cluster-wise correction)), investigators find out those specific significantly altered data (questionnaire for quality of life of urinary incontinence I-QOL, FSFI- female sexual function index assessment) that shows significant linear correlation (Pearson Correlation, p <0.05, with age as covariate) with praxiology where the brain region is a unique biomarker of brain function in patients with UUI. ②UUI patients will be divided into two groups after treatment, that is, the symptoms of urinary incontinence disappeared after treatment (abbreviated as the disappeared) and the urinary incontinence was not relieved after treatment (abbreviated as the the unrelieved). Through comparing the image parameters (F-test one-way ANOVA,two tails, p < 0.05/3=0.017 (family-wise correction)),of whole brain function among the three groups (normal control group, the disappeared group and unrelieved group), investigators will verify the second hypothesis, that is, for patients with UUI whose symptoms of urinary incontinence disappear after behavioral therapy, whether the function and structure of the brain (structural, functional and white matter connectivity) will change reversibly and return to its original state;

③ Through analysis of changes in behavioral data before and after treatment (questionnaire for quality of life of urinary incontinence I-QOL, FSFI- female sexual function index assessment) and linear correlation analysis of all-brain functional image parameters (Pearson Correlation, p < 0.05, age as covariate), investigators can verify the third hypothesis, that is, the degree of unrelieved urinary incontinence after UUI behavior therapy is significantly correlated with his / her brain function and structural changes.

8.Data analysis tools:FSL software will be applied for brain function image analysis, and MATLAB and SPSS for data statistical analysis.

Being tested
bio-feedback treatment
Medical subject headings
Urinary Incontinence, Urge

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • bio-feedback treatmentDevice

    50 patients will treated with phenix u2 and phenix u4 treating equipment。

Study groups in NCT04271852
Study groupRoleWhat they receive
UUI patientsExperimental50 UUI patients will have biofeedback treatment once a week.
Receives: Device: bio-feedback treatment
ControlNo interventionNot described

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Assessing change of the number of leakages was used to assess the severity of urinary incontinence.

    By ues of voiding diaries.The more frequent leakage, the more serious incontinence.

    Baseline:

    Measured: Baseline,3th month

  2. Brain regional gray matter density change of subjects

    All subjects will be scanned by MRI for contrasting anatomic brain image,and the brain regional gray matter density will be calculated from the contrasting anatomical image.

    Measured: Baseline,3th month

  3. Brain functional connectivity strength

    All the subjects will be scanned by MRI for functional brain images,and the brain functional connectivity strengths will be calculated from the contrasting anatomical images,with number 1presents the maximum positive connectivity between two different brain regions,number-1presents maximum negative connectivity,and number 0 presents 0 connectivity.

    The change of brain connection intensity in three months.

    Measured: Baseline,3th month

Secondary outcomes (6)
  1. Assessing change of POP-Q measurements were used to assess pelvic floor prolapse.

    POP-Q(Pelvic Organ Prolapse Quantitive examination):Contrast changes in POP-Q measurements.Measure nine point include Ab,Ba,Ap,Bp,Tvl,gh,pb,C,D.

    POP-Q is based on hymen (0 point), Six points of the anterior wall, posterior wall and the top of the vagina were used as indicator points (two points of the anterior wall, AA and Ba, two points of the posterior wall, AP and BP, two points of the top, C and D), The changes of the six points relative to the hymen were measured in scale (the indication points were negative in the inner side of the hymen margin and positive in the outer side of the hymen margin), and the prolapse was quantified.

    At the same time, total vaginal length (TVL) was recorded, At the same time, the length of gonadal hiatus (GH) was recorded At the same time, the length of perineal body (PB) was recorded. Aa、Ba、Ap、Bp:Normal range at -3cm. C、D:Normal range at -Tvl to-(Tvl-2)

    Measured: Baseline,3th month

  2. Assessing change of the number of millimeters of rectocele used to evaluate the prolapse of the posterior wall of the vagina.

    (By Urodynamic examination)Measurement of rectocele:Degree of swelling 0-15mm is mild,>15mm or above is severe.

    The degree of rectocele was compared before and after three months.

    Measured: Baseline,3th month

  3. Assessing change of the number of millimeters of prolapse used to assess the extent of prolapse.

    (By Urodynamic examination)The distance between the uterus and the margin of hymen.The unit is mm.

    Measured: Baseline,3th month

  4. Assessing change of the measurement of detrusor compliance was used to assist in the evaluation of acute incontinence.(By Urodynamic examination)

    (By Urodynamic examination)Compliance: The ratio of increased detrusor pressure to increased bladder capacity (c = △ v / △ p).(>20ml/cmH2O).Maximum bladder compliance = maximum bladder capacity ÷ (filling resting pressure-empty resting pressure).

    The compliance of bladder was higher than that of three months ago.The unit is >20ml/cmH2O.

    Measured: Baseline,3th month

  5. Assessing change of Bladder neck mobility, used to assess the presence of stress urinary incontinence.

    Bladder neck activity > 15mm, increased bladder neck activity

    Measured: Baseline,3th month

  6. Assessing change of the number of millimeters of cystocele used to evaluate the prolapse of the anterior wall of the vagina.

    (By Urodynamic examination)Measurement of cystocele:Degree of swelling 0-10mm is mild,>10mm or above is severe.

    The degree of cystocele was compared before and after three months.

    Measured: Baseline,3th month

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted17 Feb 2020
  2. Study start23 Oct 2019
  3. Primary completion31 Oct 2022 (estimated)
  4. Study completion31 Dec 2022 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Masking
None (open label)
Enrolment
100 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT04271852
Sponsor's protocol ID
SAHoWMU-CR2019-09-112
Status last verified
Mar 2020
First submitted
28 Nov 2019
Last updated
18 Mar 2020
Results posted
No
Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No

Questions about this trial

What is this clinical trial studying?

A study testing bio-feedback treatment in people with Urinary Incontinence, Urge, run by Second Affiliated Hospital of Wenzhou Medical University at 1 site in China.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 3 inclusion and 15 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: status not confirmed, as of the sponsor's last update on 18 Mar 2020. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in China. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

Results are not available in the source record.

How can a doctor refer a patient or contact the research team?

Contact Ledan Wang, Doctor (13858850907, ledanwang331@163.com), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Assessing change of the number of leakages was used to assess the severity of urinary incontinence. (time frame: Baseline,3th month). The study lists 3 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 18 Mar 2020.

Free account

Log in to keep searching

You’ve used your 3 free searches. AzTrials is free: log in or create a free account to keep searching clinical trials and save the ones you want to follow.

Create a free accountLog in