Diabetic GastroparesisEarly Phase 1ThorS-MagNTNCT04706832
Thoracic Splanchnic Magnetic Neuromodulation Therapy (ThorS-MagNT) for Grade 3 Diabetic Gastroparesis: Pilot Study
A Early Phase 1 study testing Thoracic Splanchnic Magnetic Neuromodulation Therapy in people with Diabetic Gastroparesis, run by Augusta University at 1 site in United States.
Trial 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. Read more about this study
- Who is it for?
- Ages 18 to 85 years
- Conditions the study is for
- Diabetic Gastroparesis
- What is being tested?
- Thoracic Splanchnic Magnetic Neuromodulation Therapy
- Type of treatment
- Medical device
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 7 participants
- Where
- 1 siteUnited States
- Study dates
- 5 Nov 2020to 30 Dec 2022
- Phase
- Early Phase 1
- 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 18 to 85 years
- All sexes
- No healthy volunteers
- Adult, Older adult
Who may be able to join
- Previously diagnosed diabetic gastroparesis patients admitted with persistent symptoms after correction of metabolic disturbance;
- Men or women age less than 85;
- No known mucosal disease
Who cannot join
- Postsurgical gastroparesis;
- Gastrointestinal obstruction or presence of gastric bezoar;
- Prior gastric surgery (fundoplication, gastric resection or pyloroplasty);
- Active inflammatory bowel disease;
- Eosinophilic gastroenteritis;
- Connective tissue disease;
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- Chronic liver disease;
- Use of opioids, tricyclic antidepressants;
- Active depression;
- Severe cardiac disease and arrhythmias;
- Metal implants, including gastric electrical stimulators (GES) deep brain stimulators (DBS), sacral nerve stimulators (SNS), or pacemakers;
- Pregnant women or nursing mothers.
Trial locations and contacts
1 site in 1 country.
About this study
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.
Read the detailed description
The global burden of diabetes, both type 1 (TIDM) and type 2 (T2DM), is increasing. Gastroparesis is an under-recognized and significant complication of diabetes, whose lack of effective treatment has severely handicapped diabetic management. Diabetic gastroparesis (DG) can range up to half of T1DM patients in tertiary care. Recently, a 4-fold increase in hospitalizations has been seen in DG patients with refractory symptoms despite medical therapy and inability to maintain oral nutrition - Grade 3 gastroparesis or gastric failure. A critical barrier to progress has been both a lack of pathophysiological understanding of DG and absence of effective treatments. A key dysfunction in DG is felt to be diabetic autonomic neuropathy (DAN) that causes gastric atony and segmental hypomotility of the small intestine, in addition to disruption of urinary bladder function, sudomotor, pilomotor, and vasomotor activities. Autonomic testing of DG patients in the NIDDK Gastroparesis Clinical Research Consortium (GpCRC) showed sympathetic hypofunction was the only significant abnormality that distinguished DG from diabetics with normal gastric emptying. The greater splanchnic nerve carries a mix of sympathetic and parasympathetic nerve fibers in the abdomen6. Stimulation of the thoracic dorsal roots or the greater splanchnic nerve in the thorax, pure sympathetic stimulation, may enhance gastric contractility especially in states of gastric atony or hypocontractility, as demonstrated in multiple animal studies.
Investigators have developed a novel, safe, noninvasive, and effective peripheral nerve treatment, translumbosacral neuromodulation therapy (TNT), using repetitive magnetic stimulation, for fecal incontinence (FI). In FI patients, investigators have demonstrated that TNT can correct neuropathy and improve bowel function. The goal of this study is to build on investigators' 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. Central hypothesis is that ThorS-MagNT will improve sympathetic hypofunction, gastric hypomotility/atony, and spino-gut interactions and thereby improve symptoms of DG. The impact of this work is to develop a safe, non-invasive neuromodulation therapy for severe DG.
Specific Aim #1 - Evaluation of the Safety and Effectiveness of Thoracic Splanchnic Magnetic Neuromodulation Therapy (ThorS-MagNT) in patients with Grade 3 Diabetic Gastroparesis. To test the hypothesis that ThorS-MagNT will reduce symptoms of gastroparesis, improve gastric emptying, and is well-tolerated. ThorS-MagNT is performed by low-frequency, low-intensity repetitive magnetic stimulation bilaterally around T7-8 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.
Specific Aim #2 - Determination of predictive factors for response to ThorS-MagNT for Diabetic Gastroparesis. To test the hypothesis that subjects with more severe disease as assessed by the Patient Global Impression of Severity (PGI-S), poorly controlled diabetes, increased Brain-derived neurotrophic factor (BDNF), and significant neuroinflammation will predict better response to ThorS-MagNT.
Successful completion of this proposal will establish thoracic splanchnic neuromodulation as a promising, safe, and non-invasive therapy for diabetic gastroparesis, a condition sorely lacking in effective treatments, with potential to induce neuroplastic changes along the spino-gastrointestinal pathway and result in a paradigm and conceptual shift in current management of DG.
- Conditions
- Diabetic Gastroparesis
- Being tested
- Thoracic Splanchnic Magnetic Neuromodulation Therapy
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Thoracic Splanchnic Magnetic Neuromodulation TherapyDevice
Also called ThorS-MagNT
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.
| Study group | Role | What they receive |
|---|---|---|
| ThorS-MagNT Treatment | Other | Low-frequency, low-intensity repetitive magnetic stimulation bilaterally at T7-8 intravertebral space twice a day for 5 days with a total 1200 magnetic stimulations per treatment session at 1 Hz. Receives: Device: Thoracic Splanchnic Magnetic Neuromodulation Therapy |
What is being measured
The primary outcome is the main question the study is designed to answer.
Responder rate
The responder rate is defined as an improvement in the Gastroparesis Cardinal Symptom Index-daily diary (ANMS GCSI-DD) score (e.g., >20% decrease in total symptom score from baseline) in at least 50% of the days of treatment.
Measured: 1 week
Secondary outcomes (3)
Sub-scores of the ANMS GSCI-DD
The change in 1. severity of nausea, 2. severity of early satiety, 3. severity of postprandial fullness, 4. severity of upper abdominal pain, 5. number of vomiting episodes, and 6. severity of gastroparesis during 5 days of ThorS-MagNT treatment.
Measured: 1 week
Gastric emptying time
The change in gastric emptying time after 5 days of ThorS-MagNT treatment and 14 days after treatment.
Measured: 3 weeks
Patient Global Impression of Improvement (PGI-I)
The change in Patient Global Impression of Improvement (PGI-I) score after 5 days of ThorS-MagNT treatment and 14 days after treatment.
Measured: 3 weeks
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted13 Jan 2021
- Study start5 Nov 2020
- Primary completion30 Oct 2022
- Study completion30 Dec 2022
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (1)Papers the sponsor has linked to this study.
- Other trials for Diabetic GastroparesisStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Early Phase 1
- Primary purpose
- Treatment
- Allocation
- Not applicable
- Intervention model
- Single group
- Model description
- Intervention type: FDA regulated device
- Masking
- None (open label)
- Enrolment
- 7 participants (actual)
Sponsor and investigators
- Lead sponsor
- Augusta University
- Sponsor type
- University, hospital or other
- Responsible party
- Sponsor
- Investigators
- Amol Sharma, MD, MS, Principal investigator, Augusta University
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT04706832
- Sponsor's protocol ID
- ThorS-MagNT
- Other IDs
- U24DK115255-04, U24DK076169-13
- Acronym
- ThorS-MagNT
- Status last verified
- Jan 2025
- First submitted
- 11 Jan 2021
- Last updated
- 30 Jan 2025
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- Yes
- Individual data sharing
- No
Publications
Karunaratne T, Yan Y, Eubanks A, Inman B, Rao S, Sharma A. Thoracic Spinal Nerve Neuromodulation Therapy for Diabetic Gastroparesis: A Proof-of-Concept Study. Clin Gastroenterol Hepatol. 2023 Oct;21(11):2958-2959.e3. doi: 10.1016/j.cgh.2022.09.012. Epub 2022 Sep 22. No abstract available.
PubMed 36152902
Study at a glance
From the registry record, last updated by the sponsor on 30 Jan 2025. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Thoracic Splanchnic Magnetic Neuromodulation Therapy (ThorS-MagNT) for Grade 3 Diabetic Gastroparesis: Pilot Study
- ClinicalTrials.gov ID
- NCT04706832
- Acronym / sponsor ID
- ThorS-MagNT / ThorS-MagNT
- Conditions
- Diabetic Gastroparesis
- Phase
- Early Phase 1
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 7 participants (actual)
- Lead sponsor
- Augusta UniversityUniversity, hospital or other
- Collaborators
- National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
- Study start
- 5 Nov 2020 (actual)
- Primary completion
- 30 Oct 2022 (actual)
- Study completion
- 30 Dec 2022 (actual)
- First posted
- 13 Jan 2021 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
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.
Detailed description
The global burden of diabetes, both type 1 (TIDM) and type 2 (T2DM), is increasing. Gastroparesis is an under-recognized and significant complication of diabetes, whose lack of effective treatment has severely handicapped diabetic management. Diabetic gastroparesis (DG) can range up to half of T1DM patients in tertiary care. Recently, a 4-fold increase in hospitalizations has been seen in DG patients with refractory symptoms despite medical therapy and inability to maintain oral nutrition - Grade 3 gastroparesis or gastric failure. A critical barrier to progress has been both a lack of pathophysiological understanding of DG and absence of effective treatments. A key dysfunction in DG is felt to be diabetic autonomic neuropathy (DAN) that causes gastric atony and segmental hypomotility of the small intestine, in addition to disruption of urinary bladder function, sudomotor, pilomotor, and vasomotor activities. Autonomic testing of DG patients in the NIDDK Gastroparesis Clinical Research Consortium (GpCRC) showed sympathetic hypofunction was the only significant abnormality that distinguished DG from diabetics with normal gastric emptying. The greater splanchnic nerve carries a mix of sympathetic and parasympathetic nerve fibers in the abdomen6. Stimulation of the thoracic dorsal roots or the greater splanchnic nerve in the thorax, pure sympathetic stimulation, may enhance gastric contractility especially in states of gastric atony or hypocontractility, as demonstrated in multiple animal studies.
Investigators have developed a novel, safe, noninvasive, and effective peripheral nerve treatment, translumbosacral neuromodulation therapy (TNT), using repetitive magnetic stimulation, for fecal incontinence (FI). In FI patients, investigators have demonstrated that TNT can correct neuropathy and improve bowel function. The goal of this study is to build on investigators' 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. Central hypothesis is that ThorS-MagNT will improve sympathetic hypofunction, gastric hypomotility/atony, and spino-gut interactions and thereby improve symptoms of DG. The impact of this work is to develop a safe, non-invasive neuromodulation therapy for severe DG.
Specific Aim #1 - Evaluation of the Safety and Effectiveness of Thoracic Splanchnic Magnetic Neuromodulation Therapy (ThorS-MagNT) in patients with Grade 3 Diabetic Gastroparesis. To test the hypothesis that ThorS-MagNT will reduce symptoms of gastroparesis, improve gastric emptying, and is well-tolerated. ThorS-MagNT is performed by low-frequency, low-intensity repetitive magnetic stimulation bilaterally around T7-8 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.
Specific Aim #2 - Determination of predictive factors for response to ThorS-MagNT for Diabetic Gastroparesis. To test the hypothesis that subjects with more severe disease as assessed by the Patient Global Impression of Severity (PGI-S), poorly controlled diabetes, increased Brain-derived neurotrophic factor (BDNF), and significant neuroinflammation will predict better response to ThorS-MagNT.
Successful completion of this proposal will establish thoracic splanchnic neuromodulation as a promising, safe, and non-invasive therapy for diabetic gastroparesis, a condition sorely lacking in effective treatments, with potential to induce neuroplastic changes along the spino-gastrointestinal pathway and result in a paradigm and conceptual shift in current management of DG.
Study design
- Primary purpose
- Treatment
- Allocation
- Not applicable
- Intervention model
- Single group
- Masking
- None (open label)
- Number of arms
- 1
- Model description
- Intervention type: FDA regulated device
| Arm | Type | Receives |
|---|---|---|
| ThorS-MagNT Treatment | Other | Device: Thoracic Splanchnic Magnetic Neuromodulation TherapyLow-frequency, low-intensity repetitive magnetic stimulation bilaterally at T7-8 intravertebral space twice a day for 5 days with a total 1200 magnetic stimulations per treatment session at 1 Hz. |
Who may qualify
- Ages
- 18 to 85 years
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (3 listed)
- Previously diagnosed diabetic gastroparesis patients admitted with persistent symptoms after correction of metabolic disturbance;
- Men or women age less than 85;
- No known mucosal disease
Key exclusion criteria (12 listed)
- Postsurgical gastroparesis;
- Gastrointestinal obstruction or presence of gastric bezoar;
- Prior gastric surgery (fundoplication, gastric resection or pyloroplasty);
- Active inflammatory bowel disease;
- Eosinophilic gastroenteritis;
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Thoracic Splanchnic Magnetic Neuromodulation TherapyAlso: ThorS-MagNTThorS-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. | Device | ThorS-MagNT Treatment |
Primary outcome
Responder rate
Time frame: 1 week
The responder rate is defined as an improvement in the Gastroparesis Cardinal Symptom Index-daily diary (ANMS GCSI-DD) score (e.g., >20% decrease in total symptom score from baseline) in at least 50% of the days of treatment.
3 secondary outcomes
Sub-scores of the ANMS GSCI-DD
Time frame: 1 week
Gastric emptying time
Time frame: 3 weeks
Patient Global Impression of Improvement (PGI-I)
Time frame: 3 weeks
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 30 Jan 2025.
- Derived from this study: PubMed 36152902Karunaratne T, Yan Y, Eubanks A, Inman B, Rao S, Sharma A. Thoracic Spinal Nerve Neuromodulation Therapy for Diabetic Gastroparesis: A Proof-of-Concept Study. Clin Gastroenterol Hepatol. 2023 Oct;21(11):2958-2959.e3. doi: 10.1016/j.cgh.2022.09.012. Epub 2022 Sep 22. No abstract available.
- Individual participant dataSharing planned: No
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Amol Sharma, MD, MS principal investigator
Augusta University
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A Early Phase 1 study testing Thoracic Splanchnic Magnetic Neuromodulation Therapy in people with Diabetic Gastroparesis, run by Augusta University at 1 site in United States.
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 12 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: finished, as of the sponsor's last update on 30 Jan 2025. 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 United States. 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.
What does this phase mean?
Early Phase 1 (sometimes called Phase 0) studies give a very small amount of a treatment to a few people, mainly to see how the body handles it.
Not every study follows the same path, and some studies (observational studies, device studies) have no phase.
Are results available for this study?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Responder rate (time frame: 1 week). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
On the ClinicalTrials.gov record for NCT04706832, which also lists 1 linked publication.
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 30 Jan 2025.