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Completed

NCT Number: NCT03638843

Endoscopic Gastric Mucosal Devitalization (GMD) as a Primary Obesity Therapy - Part 2

Rapid metabolic improvements seen with sleeve gastrectomy are likely a result of changes in gastric origin. The gastric mucosa is an endocrine organ that regulates satiation pathways and is a complex regulator of food intake as well as lipid and glucose metabolism. This study aims to assess the efficacy and safety of endoscopic selective gastric mucosal devitalization (GMD) for the management of obesity and its related comorbidities.

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Key information

Age range

28 year–60 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Johns Hopkins Medical Institutions

Baltimore, Maryland, 21287, United States

About this study

Endoscopic approaches to obesity may help fulfill the unmet need of over half the US adult population that would benefit from therapy for obesity but are not receiving it. Endoscopic approaches to obesity have the potential to be more efficacious than antiobesity medications and have a lower risk-cost profile compared with bariatric surgery.

Endoscopic approaches to obesity need to be increasingly modeled on the proposed mechanisms contributing to the benefits of bariatric surgery.

The investigators seek to decipher if the gastric mucosa is an independent regulator of food intake, body weight, lipid and glucose metabolism and serum gut hormones. The investigators also wish to ascertain if selective devitalization of the gastric mucosa, without alteration in gastric volume, will improve obesity related comorbidities.

This study will be divided into 3 parts. The purpose of completing the 3 phases is to develop a minimally invasive weight loss technique that is effective, safe and ready for more rigorous assessment via a future randomized control trial.

Objectives:

Overall:

To assess the efficacy and safety of gastric mucosal devitalization for the management of obesity and its related comorbidities.

Part 2:

Aims to confirm that the optimal color of the tissue identified by part 1 corresponds to selective mucosal devitalization in the in vivo setting by histopathologic examination. For this, patients will be enrolled in the study after being scheduled to undergo vertical sleeve gastrectomy (VSG). GMD will be performed three days prior to the VSG, and the excised tissue including devitalized gastric mucosa will be evaluated. The degree and correlation of devitalization with mucosal discoloration will be assessed.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Patients scheduled to undergo vertical sleeve gastrectomy

Exclusion criteria

  • Age under 28 or older than 60
  • Insulin dependent Diabetes Mellitus
  • Suspected or biopsy confirmed liver cirrhosis
  • Significant ethanol consumption >21 drinks/week in men and >14 drinks/week in women
  • Presence of other chronic liver disease including hepatitis B-C, autoimmune hepatitis, alpha 1 antitrypsin deficiency, Wilson's disease, and hemochromatosis
  • Pregnant or breast-feeding
  • Patients who already have an intragastric balloon or other gastric implant
  • Patients with gastroesophageal reflux disease
  • Patients with previous gastric surgeries, altered gastrointestinal anatomy such as Billroth I, Billroth II, roux-en-y gastrectomy, roux-en-y hepaticojejunostomy, or any restrictive or bypass bariatric surgery
  • Patients with previous gastric embolization for obesity
  • Presence of inflammatory disorder of the gastrointestinal tract
  • Patients with active peptic ulcer disease
  • Patients with gastroesophageal varices
  • Presence of a large hiatal hernia (grade IV on Hills classification: large hiatal hernia and essentially no fold approximating the endoscope in the retroflexed view and where the lumen of the esophagus is gaping open allowing the squamous epithelium to be seen)
  • Structural abnormality in the esophagus or pharynx
  • Have major esophageal motility disorders as per the Chicago classification including achalasia, diffuse esophageal spasm, jackhammer esophagus, and Esophagogastric junction outflow obstruction
  • Mucosal or submucosal gastric mass that is clinically suspected to be of malignant nature
  • Severe clotting or bleeding disorder
  • Other medical condition that does not allow for endoscopic procedure
  • Severe psychiatric illness
  • Unable to participate in routine medical follow-up
  • On antiplatelet agents including clopidogrel, ticlopidine, prasugrel, and cangrelor. acetylsalicylic acid use will be allowed
  • On anticoagulants including heparin, warfarin, dabigatran, rivaroxaban, apixaban, and edoxaban

Treatment and study plan

Gastric mucosal devitalization

Procedure

Gastric mucosal devitalization is an endoscopic procedure which uses argon plasma coagulation to result in selective damage to the gastric mucosa and submucosa.

Primary outcomes

  1. Pathological changes

    Time frame: 6 months

    Histopathological assessment to determine whether selective devitalization of mucosa and submucosa corresponds with decolorization during the in-vivo procedure.

Secondary outcomes

  1. Technical feasibility

    Time frame: 6 months

    Feasibility of retroflexion technique during the in-vivo devitalization procedure assessed by the endoscopist.

  2. Procedural tolerability

    Time frame: 6 months

    Tolerability of gastric mucosal devitalization after the post-procedural follow up assessed by the endoscopist

Sponsors and collaborators

Lead sponsor

Johns Hopkins University

Other

Collaborators

  • Erbe USA Incorporated

Registry information

Important dates

Study start
2020
Primary completion
2021
Study completion
2021
First posted
Aug 20, 2018
Registry last updated
Jul 20, 2021

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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