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Neuromodulation
Neuromodulation for Bowel Incontinence (TNT Trial)
N/A
Recruiting
Research Sponsored by Augusta University
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
On a 2-week stool diary patients reported at least one episode of solid or liquid FI/week
Recurrent episodes of FI for 6 months
Must not have
rectal prolapse
Ulcerative and Crohn's colitis
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 6 weeks, 48 weeks
Summary
This trial is testing a new treatment called Translumbosacral Neuromodulation Therapy (TNT) for people with fecal incontinence (FI), especially women and elderly individuals. TNT uses magnetic pulses to stimulate nerves in the lower back, helping to improve control over bowel movements. The goal is to provide a more effective, non-invasive treatment option for those who struggle with FI.
Who is the study for?
This trial is for adults who've had bowel incontinence for at least 6 months, with weekly episodes. They must not have mucosal diseases, be on opioids, or have a range of other conditions like Crohn's disease, severe heart issues, metal implants near the treatment area, pacemakers, or certain past surgeries.
What is being tested?
The study tests Translumbosacral Neuromodulation Therapy (TNT) against a sham (fake) therapy to see if TNT can improve bowel control by stimulating nerves with magnetic fields. It aims to find the best dose and understand how it works over short and long terms.
What are the potential side effects?
While specific side effects are not listed here, non-invasive magnetic stimulation therapies like TNT may cause discomfort at the site of application or mild headaches. Serious side effects are rare but could include seizures in susceptible individuals.
Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowSelect...
I have had at least one episode of incontinence per week.
Select...
I have had recurring episodes of fecal incontinence for 6 months.
Exclusion Criteria
You may be eligible for the trial if you check “No” for criteria below:Select...
I have a condition where part of my rectum sticks out of my anus.
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I have been diagnosed with either ulcerative colitis or Crohn's disease.
Select...
I do not have severe heart issues, chronic kidney failure, or major GI surgery history except for gallbladder or appendix removal.
Select...
I have no active issues like anal fissures, abscesses, malformations, fistulae, or severe hemorrhoids.
Select...
I experience severe diarrhea, with more than 6 liquid stools a day.
Select...
I have had a radical hysterectomy or pelvic surgery/radiation.
Select...
I have a neurological condition like epilepsy or MS, or have had a serious head injury.
Select...
I am currently experiencing depression.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 6 weeks,4 8 weeks
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~6 weeks,4 8 weeks
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
AIM 1 measure is the proportion of patients achieving >50% of reduction in fecal incontinence episodes/weeks at the end of 6 weeks compared to baseline.
AIM 2: Latencies for lumbo-anal Magnetic Evoked Potentials (MEP) responses compared to baseline
AIM 2: Latencies for sacro-anal MEP responses compared to baseline
+5 moreSecondary study objectives
Amplitudes (Milivolts of the nerve) for lumbo-rectal MEP compared to baseline
Amplitudes (Milivolts of the nerve) for recto-cortical CEP responses
Amplitudes (Milivolts of the nerve) for sacro-rectal MEP
+24 moreTrial Design
3Treatment groups
Active Control
Placebo Group
Group I: 1 Hz 2400 TNT TreatmentActive Control1 Intervention
Intervention: TNT treatment intervention with 2400 total stimulations with the magnetic coil..
Group II: 1 Hz 3600 TNT TreatmentActive Control1 Intervention
Intervention: TNT treatment intervention with 3600 total stimulations with the magnetic coil.
Group III: Sham TNT TreatmentPlacebo Group1 Intervention
This arm will have the sham treatment session. First we will assess the motor threshold intensity described above. Next, a sham coil is placed on each of 4 regions (2 lumbar \& 2 sacral), and 600 stimulations will be given at each site in 2 trains, with a 5 minutes rest period between each site and 3 minutes between trains.
Research Highlights
Information in this section is not a recommendation. We encourage patients to speak with their healthcare team when evaluating any treatment decision.Mechanism Of Action
Side Effect Profile
Prior Approvals
Other Research
The most common treatments for Bowel Incontinence, such as Translumbosacral Neuromodulation Therapy (TNT), work by enhancing neural excitability and inducing neuroplasticity. These mechanisms improve sensory and motor control by modulating neuronal perturbations, which in turn enhance bidirectional gut-brain signaling, anal sphincter strength, and rectal sensation.
This is important for Bowel Incontinence patients as it offers a durable, non-invasive, and low-risk treatment option that addresses the underlying neurobiologic dysfunctions contributing to their condition.
Find a Location
Who is running the clinical trial?
Massachusetts General HospitalOTHER
3,010 Previous Clinical Trials
13,308,888 Total Patients Enrolled
Augusta UniversityLead Sponsor
215 Previous Clinical Trials
85,558 Total Patients Enrolled
National Institutes of Health (NIH)NIH
2,811 Previous Clinical Trials
8,161,126 Total Patients Enrolled
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:- You are pregnant.I have had at least one episode of incontinence per week.I have a condition where part of my rectum sticks out of my anus.I have been diagnosed with either ulcerative colitis or Crohn's disease.I do not have severe heart issues, chronic kidney failure, or major GI surgery history except for gallbladder or appendix removal.I have no active issues like anal fissures, abscesses, malformations, fistulae, or severe hemorrhoids.I experience severe diarrhea, with more than 6 liquid stools a day.I have had a radical hysterectomy or pelvic surgery/radiation.I have a neurological condition like epilepsy or MS, or have had a serious head injury.You are currently taking opioids for pain management.I am currently experiencing depression.I have had recurring episodes of fecal incontinence for 6 months.
Research Study Groups:
This trial has the following groups:- Group 1: Sham TNT Treatment
- Group 2: 1 Hz 2400 TNT Treatment
- Group 3: 1 Hz 3600 TNT Treatment
Awards:
This trial has 0 awards, including:Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
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