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NCT Number: NCT06582576

Mechanisms of Action for the Enterra Medical Gastric Electrical Stimulator

Background: Gastric electrical stimulation applied by a surgically implanted device effectively alleviates upper gastrointestinal symptoms in the majority of individuals with medically refractory gastroparesis. Despite its efficacy, the mechanisms of action have been minimally explored in previous studies, and it is unknown why some individuals experience limited symptom-lowering effects.

Aim: The investigators aim to investigate two of the potential mechanisms of action leading to symptom-reducing effects of gastric electrical stimulation: 1) possible central effects in the brainstem and brain by enhanced parasympathetic vagal activity, and 2) peripheral effects in the stomach by improved gastric accommodation.

Methods: Up to thirty individuals with drug-refractory gastroparesis having an implanted gastric electrical stimulator will be enrolled in this cross-sectional and observational study. Of these, 15 will be responders (substantial symptomatic improvement) and 15 non-responders (minor symptomatic improvement). Electroencephalography (EEG) will evaluate the stimulation-induced activity in the brain and brainstem to assess whether the gastric stimulation generates evoked potentials. Electrocardiography (ECG) will investigate stimulation-induced changes in the autonomic regulation of the heart. Gastric ultrasound will investigate the effect of stimulation on stomach accommodation, contractions, and wall tension. These central and peripheral measures will be assessed during one study day before and after activating the gastric electrical stimulator, following an increase in stimulation intensity and post-meal consumption. Furthermore, results will be compared between responders and non-responders.

Perspectives: Adjusting the parameters of gastric electrical stimulation based on objective markers in the brain, heart, or stomach, rather than relying on symptom fluctuations, may enhance the effectiveness of symptom improvement. In the future, these objective markers may aid in differentiating between responders and non-responders, which may lead to optimised selection criteria for surgery.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Department of hepatology and gastroenterology, Aarhus University Hospital

Aarhus N, 8200, Denmark

Location status: Recruiting

Location contact

Ditte Kornum, MD

CONTACT

[email protected]

Klaus Krogh, MD

CONTACT

[email protected]

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Age 18 and above
  • Able to read and understand Danish
  • Have an implanted gastric electrical stimulator for treating gastroparesis
  • Answering 0 or 1 (non-responders) or 3 or 4 (responders) on the Likert scale describing the symptom improvement gained by gastric electrical stimulation.
  • Personally signed and dated the informed consent documents ("Informeret samtykke") indicating that the patient has been informed of all pertinent aspects of the trial
  • Are willing and able to comply with the scheduled visit and trial procedures

Exclusion criteria

  • Previous surgery on the vagus nerve, including cervical vagotomy
  • Prior thoracic, abdominal or brain surgeries that, in the opinion of the investigator, could limit data collection or interpretation.
  • Previous diagnosis or history of orthostatic intolerance, e.g. POTS, neurocardiogenic syncope, orthostatic hypotension or autonomic dysfunction.
  • Patients with an implanted cardiac device (e.g. pacemaker, CRT, etc.) or vagal nerve stimulator (VNS).
  • History of neurological disease that, in the opinion of the investigator, could limit data collection or interpretation.
  • Participants with any clinical abnormalities that, in the opinion of the investigator, may increase the risk associated with trial participation or may interfere with the interpretation of the trial results

Treatment and study plan

Effect of different gastric electrical stimulator stimulation paragdimes on brain, heart, and stomach.

Diagnostic Test

Measuring EEG, ECG, and ultrasound in both groups during different stimulation intensities provided by the previously implanted gastric electrical stimulator.

Primary outcomes

  1. Evoked brain potentials

    Time frame: 5min during maximum stimulation intensity

    Amplitude of evoked brain potentials induced by gastric electrical stimulation

Secondary outcomes

  1. EEG measures between ON/OFF stimulation

    Time frame: 5min

    EEG frequency distribution when comparing the OFF and ON stimulation modes

  2. Meal-related EEG measures

    Time frame: 5min

    EEG frequency distribution in response to an ingested meal when comparing the OFF and ON stimulation modes.

  3. ECG measures between ON/OFF stimulation

    Time frame: 5min

    Heart rate variability, periodic repolarisation dynamic, and the deceleration capacity of the heart rate when comparing the OFF and ON stimulation modes.

  4. ECG measures between stimulation intensities

    Time frame: 5min

    Heart rate variability, periodic repolarisation dynamic, and the deceleration capacity of the heart rate following different stimulation intensities.

  5. Meal-related ECG measures

    Time frame: 5min

    Heart rate variability, periodic repolarisation dynamic, and the deceleration capacity of the heart rate in response to an ingested meal when comparing the OFF and ON stimulation modes.

  6. Meal-related gastric accomodation

    Time frame: 5min

    Gastric accommodation in response to an ingested meal comparing OFF and ON stimulation.

  7. Meal-related gastric tension

    Time frame: 5min

    Gastric tension in response to an ingested meal comparing OFF and ON stimulation.

  8. Meal-related gastric contraction frequency

    Time frame: 5min

    Gastric contraction frequency in response to an ingested meal comparing OFF and ON stimulation.

  9. Symptoms and gastric measures

    Time frame: 5min

    Correlation between gastroparesis symptoms (Gastroparesis Cardinal Symptom Index) and changes in gastric accommodation/tension when turning the stimulation ON after meal ingestion.

Study contacts

Contact information is provided by the study sponsor or research team.

Asbjørn Drewes, MD

CONTACT

[email protected]

29465969

Ditte Kornum, MD

CONTACT

[email protected]

40517858

Sponsors and collaborators

Lead sponsor

University of Aarhus

Other

Collaborators

  • Aalborg University Hospital
  • Aarhus University Hospital

Registry information

Official study title

Investigation of the Putative Mechanisms Underlying the Symptom-lowering Effect of the Enterra Medical Gastric Electrical Stimulator for Gastroparesis Treatment

Important dates

Study start
2024
Primary completion
2025
Study completion
2025
First posted
Sep 3, 2024
Registry last updated
Sep 19, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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