Thoracic Splanchnic Magnetic Neuromodulation Therapy (ThorS-MagNT) for Grade 3 Diabetic Gastroparesis: Pilot Study
NCT04706832 · Status: COMPLETED · Phase: EARLY_PHASE1 · Type: INTERVENTIONAL · Enrollment: 7
Last updated 2025-01-30
Summary
Diabetic gastroparesis (DG) is an under recognized and significant complication of diabetes with lack of effective treatments. Recently, a 4-fold increase in hospitalizations has been seen in DG patients with refractory symptoms, defined as Grade 3 gastroparesis. A critical barrier to progress has been both a lack of pathophysiological understanding of DG and absence of effective treatments. Diabetic autonomic neuropathy is felt to be a key dysfunction in DG that causes gastric atony and segmental hypomotility of the small intestine. Autonomic testing of DG patients reveals significant sympathetic hypofunction, a feature distinguishing DG from diabetics with normal gastric emptying. Therefore, stimulation of the thoracic dorsal roots of the greater splanchnic nerve (sympathetic stimulation) could enhance gastric motility, as observed in animal models, and improve DG.
Investigators have developed a novel, safe, noninvasive peripheral nerve treatment using repetitive magnetic stimulation, and have demonstrated improvement in fecal incontinence with neuropathy. The goal of this study is to build on our expertise to conduct a pilot, feasibility study by examining the effect of Thoracic Splanchnic Magnetic Neuromodulation Therapy (ThorS-MagNT) in patients with Grade 3 DG. The aims are to evaluate the safety, effectiveness and feasibility of ThorS-MagNT in patients with Grade 3 DG and to evaluate predictive factors of treatment. The central hypothesis is that ThorS-MagNT will improve sympathetic hypofunction, gastric motility, and spino-gut interactions, and thereby, improve symptoms of DG.
ThorS-MagNT will be performed in 12 patients hospitalized with severe DG by using low-frequency, low-intensity repetitive magnetic stimulation, bilaterally, around T7 intravertebral space, twice a day for 5 days, with a total 1200 magnetic stimulations per treatment session at 1 Hz. The primary outcome is responder rate, defined as ≥20% reduction in the Gastroparesis Cardinal Symptom Index-daily diary (ANMS GCSI-DD) score. Secondary outcomes include subscores of the ANMS GSCI-DD, effects on gastric emptying time, Patient Global Impression of Improvement (PGI-I), safety, and tolerability. The impact of this work is to develop a novel, safe, and non-invasive treatment for severe DG that could result in a paradigm shift in management of DG.
Conditions
- Diabetic Gastroparesis
Interventions
- DEVICE
-
Thoracic Splanchnic Magnetic Neuromodulation Therapy
ThorS-MagNT is performed by low-frequency, low-intensity repetitive magnetic stimulation bilaterally around T7-8 intervertebral space twice a day for 5 days with a total 1200 magnetic stimulations per treatment session at 1 Hz.
Sponsors & Collaborators
-
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
collaborator NIH -
Augusta University
lead OTHER
Principal Investigators
-
Amol Sharma, MD, MS · Augusta University
Study Design
- Allocation
- NA
- Purpose
- TREATMENT
- Masking
- NONE
- Model
- SINGLE_GROUP
Eligibility
- Min Age
- 18 Years
- Max Age
- 85 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2020-11-05
- Primary Completion
- 2022-10-30
- Completion
- 2022-12-30
- FDA Device
- Yes
Countries
- United States
Study Locations
More Related Trials
-
Multi-Channel Gastric Electrical Stimulation for the Treatment of Gastroparesis
NCT00595621 ·Status: COMPLETED ·Phase: NA
-
Safety and Efficacy of IV Infusion of Investigational Agent (TZP-101) in Patients With Severe Diabetic Gastroparesis
NCT00612014 ·Status: COMPLETED ·Phase: PHASE2
-
Evaluating the Safety and Efficacy of Tradipitant vs. Placebo in Idiopathic and Diabetic Gastroparesis
NCT04028492 ·Status: COMPLETED ·Phase: PHASE3
-
Temporary Gastric Electrical Stimulation for Drug Refractory Gastroparesis
NCT00432835 ·Status: COMPLETED ·Phase: PHASE3
-
Safety and Efficacy of IV Infusion of Investigational Agent (TZP-101) in Patients With Diabetic Gastroparesis
NCT00639808 ·Status: COMPLETED ·Phase: PHASE1
-
Enterra Therapy Clinical Study (Gastric Stimulation for Gastroparesis)
NCT00157755 ·Status: TERMINATED ·Phase: NA
-
Escalating Temporary Gastric Electrical Stimulation (GES) for Severe Gastroparesis
NCT02164591 ·Status: TERMINATED
-
Phase 2 Study of Velusetrag in Diabetic or Idiopathic Gastroparesis
NCT01718938 ·Status: COMPLETED ·Phase: PHASE2
-
Gastric Electrical Stimulation (GES) and Pyloroplasty for the Treatment of Gastroparesis
NCT03123809 ·Status: COMPLETED ·Phase: NA
-
Study of Enhanced Programming Stimulation with the Enterra® Therapy System
NCT06560307 ·Status: RECRUITING ·Phase: NA
-
Temporary Gastric Electrical Stimulation for Gastroparesis
NCT01054794 ·Status: COMPLETED ·Phase: NA
-
Gastric vs Jejunal Feeding in Diabetic Gastroparesis
NCT00944593 ·Status: WITHDRAWN ·Phase: PHASE4
-
Feasibility of Aerodigestive Stimulation Therapy Trial
NCT06118697 ·Status: RECRUITING ·Phase: NA
-
Single-Patient Expanded Access Protocol for Tradipitant In A Single Patient With Gastroparesis
NCT04474990 ·Status: AVAILABLE
-
Release of Acetylcholine From the Ganglionated Plexus During the Thaw Phase of Cryoballon Pulmonary Vein Ablation (GP RESPONSE Study)
NCT03636100 ·Status: TERMINATED
-
Neuromuscular Electrical Stimulation (NMES) for Dysphagia in Neonates
NCT02007759 ·Status: TERMINATED ·Phase: NA
-
Feasibility Study to Evaluate Safety of Nutriseal™ Nutriplace™ System
NCT03371160 ·Status: TERMINATED ·Phase: NA
-
Esophageal Food Impaction
NCT03305848 ·Status: COMPLETED ·Phase: PHASE4
-
The Diabetic and Idiopathic Gastroparesis Efficacy, Safety, and Tolerability (DIGEST) Study
NCT02267525 ·Status: COMPLETED ·Phase: PHASE2
-
Comparison of Two Endoscopically Placed Nasojejunal Probes
NCT02705027 ·Status: UNKNOWN ·Phase: NA
-
Intraumbilical Amino Acids and Glucose Supplementation Via Port by Severe IUGR in Human Fetuses
NCT02596594 ·Status: COMPLETED ·Phase: NA
-
Safety and Efficacy Study of Teduglutide in Subjects With Short Bowel Syndrome
NCT00081458 ·Status: COMPLETED ·Phase: PHASE3
-
Small Volume Plasma Exchange (SVPE) for Guillain-Barré Syndrome (GBS) Patients
NCT02780570 ·Status: COMPLETED ·Phase: PHASE2
-
Prospective Monocentric Study on the Efficacy of Lidocain Spray for Patient Comfort During Nasogastric Tube Insertion in Enteral Nutrition
NCT02022059 ·Status: COMPLETED ·Phase: PHASE3
-
Short Bowel Syndrome and Teduglutide Versus Placebo
NCT02099084 ·Status: COMPLETED ·Phase: PHASE4