Actively Recruiting

Phase 1
Age: 18Years - 85Years
All Genders
NCT05273788

Thoracic Neuromodulation for Diabetic Gastroparesis

Led by Medical University of South Carolina · Updated on 2025-09-03

48

Participants Needed

1

Research Sites

200 weeks

Total Duration

On this page

Sponsors

M

Medical University of South Carolina

Lead Sponsor

N

National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)

Collaborating Sponsor

AI-Summary

What this Trial Is About

The global incidence of diabetes is rising. Gastroparesis is a significant complication of diabetes that results in debilitating symptoms and affects quality of life. Current treatment options for diabetic gastroparesis are limited. Significant visceral afferent neuropathy is associated with diabetic gastroparesis and sympathetic overactivity is seen in nausea, both type 1 and 2 diabetes, and diabetic complications. These dysfunctions can result from neuropathy affecting the thoracic spinal nerves that carry both general visceral afferents and preganglionic sympathetic efferents in the greater splanchnic nerve, innervating the foregut. Neuromodulation of the thoracic spinal nerves should improve diabetic gastroparesis symptoms and restore quality of life by improving neuropathy and gastric sensori-motor function. The investigators has developed and refined a novel, noninvasive, neuromodulation treatment, Thoracic Spinal Nerve Magnetic Neuromodulation Therapy (ThorS-MagNT). In an uncontrolled trial of adults with diabetic gastroparesis, ThorS-MagNT the investigators demonstrated feasibility, acceptability, and improvement of DGp symptoms. Whether active neuromodulation is better than sham therapy and the optimal frequency of treatment are not known. The investigators propose to conduct a dose-ranging, sham-controlled trial (pilot NIH Stage 1b) to assess the effect of ThorS-MagNT on symptom severity and quality of life in diabetic gastroparesis (TNM-DGp Trial). The investigators will test the hypothesis that ThorS-MagNT will improve visceral afferent neuropathy, autonomic and gastric dysfunction, compared to sham. The investigators will also test whether any improvements are due to neuromodulation of (a) peripheral spino-gut axis or (b) central structures of the limbic system and autonomic network, or both. Successful completion of this pilot study will provide insights into gastroparesis disease processes and inform mechanisms of action of neuromodulation therapy in addressing disruption of the brain-gut axis. Expected outcomes include development of a novel, non-invasive, safe and efficacious therapy for diabetic gastroparesis. These efforts will inform future true efficacy testing in an NIH Stage 2 trial using multiphase optimization strategy (MOST) design.

CONDITIONS

Official Title

Thoracic Neuromodulation for Diabetic Gastroparesis

Who Can Participate

Age: 18Years - 85Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Outpatient with diabetic gastroparesis and moderate to severe symptoms with a total ANMS GCSI-DD score of 2.0 or higher during screening
  • Men or women younger than 85 years old
  • No known mucosal disease
  • Able to speak, write, and understand English
  • On stable doses of medications for at least 30 days before the study, excluding psychotropic drugs, opioids, and illicit drugs, and agree not to change medications during the study
Not Eligible

You will not qualify if you...

  • Having postsurgical gastroparesis
  • Gastrointestinal obstruction
  • Previous gastric surgery such as fundoplication, gastric resection, or pyloroplasty
  • Diagnosed with achalasia, chronic intestinal pseudo-obstruction, or colonic inertia with fewer than one complete spontaneous bowel movement every two weeks
  • Active inflammatory bowel disease
  • Using opioids more than three times a week or marijuana more than five times a week
  • Changed neuromodulator medication doses in the last three months
  • Using sympathomimetic drugs
  • History of seizures or seizure disorders
  • Active serious psychiatric illness needing independent attention
  • Severe or unstable heart disease and arrhythmias
  • Having metal implants that are not safe for MRI, gastric electrical stimulators, deep brain stimulators, sacral nerve stimulators, or pacemakers
  • Pregnant or breastfeeding women
  • Receiving enteral or parenteral feeding

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Augusta University

Augusta, Georgia, United States, 30912

Actively Recruiting

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How is the study designed?

Study Type

INTERVENTIONAL

Masking

QUADRUPLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

3

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