Fact CheckerSign in

NCT02933554Not yet recruiting

Bariatric Embolization of Arteries for the Treatment of Nonalcoholic Steatohepatitis

A Single Center, Non-randomized Study to Evaluate the Safety and Efficacy of Left Gastric Artery Embolization, to Promote Short-term Weight Loss in Obese Patients With Nonalcoholic Steatohepatitis (NASH) and Thereby Improve NASH

Source: ClinicalTrials.gov · Last updated 28 Jul 2025 · Not updated for over 12 months - ask the site whether it is still open

Brief summary (registry, in English)

Obesity is an epidemic in the US. With progression of obesity, Nonalcoholic steatohepatitis (NASH) has been a growing public health issue. Presently there is no cure for NASH.Prevention of progression of fibrosis in NASH is crucial, as they are at a high risk for cirrhosis and may need liver transplant. Recent studies have shown that blocking blood vessels to a particular portion of the stomach (bariatric or left gastric artery embolization) can temporarily decrease levels of the appetite inducing hormone ghrelin, and result in weight loss.The purpose of this study is to determine if Left gastric artery embolization (LGAE) in patients with obesity and NASH leads to clinically significant weight loss with improvement of NASH.

Status (registry)
Not yet recruiting
Study type
Interventional
Enrollment
8 (estimated)
First submitted
11 Oct 2016
Start date
1 Dec 2025
Primary completion date
30 Jun 2026
Lead sponsor
Keith Pereira, MD:
NCT number
NCT02933554

What you commit to

  • Study type: Interventional
  • Planned participants: 8
  • From 1 Dec 2025 to the primary completion date, 30 Jun 2026
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Subjects requiring any anticoagulant medications should be excluded if radial access cannot be obtained.
  • Subjects who are taking aspirin/ NSAIDs and in whom these medications are unable to be withdrawn from aspirin and NSAIDs for at least 3 days prior to the LGAE procedure and for 30 days following the LGAE procedure (because of the potential risks of gastric bleeding following the procedure).
  • prior surgical weight loss procedures including gastroplasty, jejunoileal, or jejunocolic bypass, total parenteral nutrition within the past 6 months; Prior history of gastric pancreatic, hepatic, and/or splenic surgery
  • Prior embolization to the stomach, spleen or liver, unless the prior embolization was a transarterial chemoembolization (TACE) to the liver for HCC.
  • If review of available prior imaging studies (i.e CT, MRI, or US)shows potential anatomical variations, presence of severe atheromatous disease, large arteriovenous shunting of blood.
  • Patient taking hepatotoxic drugs. List of drugs causing steatohepatitis include but are not limited to: amiodarone, chemotherapy (5-fluorouracil, tamoxifen, irinotecan, cisplatin, and asparaginase), glucocorticoids, methotrexate, sulfonamides, antithyroid drugs, phenytoin, tetracyclines, isoniazid, salicylates, and valproic acid.
  • Patients taking other trial medications for NASH.

Other illness

  • Significant psychiatric problems, severe enough to cause suffering or a poor ability to function in life. Center for Epidemiological Studies Depression (CESD) score \> or = 16 without psychiatric evaluation. \[If Center for Epidemiological Studies Depression (CESD) score \> or =16 AND is in care of behavior health specialist who has indicated patient has adequate coping mechanisms to undergo procedure and does not foresee mental health as barrier to participation in study.\]
  • Presence of systemic illness or other medical conditions relevant to survival .(Note that in the HCC pre liver transplant cohort, the presence of HCC will not be considered an exclusion criteria)
  • Metastatic cancer
  • Evidence of decompensated liver disease (uncontrolled ascites, or uncontrolled spontaneous encephalopathy)
  • Abnormal Endoscopy - large sliding hiatal hernia or paraesophageal hernia, active peptic ulcer disease, active H. pylori infection
  • History of abnormal Nuclear Gastric Motility examination-defined as delayed emptying of gastric contents \> 90%, 60% and 10% at 1 hour, 2 hours, and 4 hours respectively.
  • Known aortic disease, such as dissection or aneurysm; peripheral arterial disease or other cardiovascular disease.
  • Type 2 diabetes on anti-diabetic medications that are known to cause hypoglycemia. e.g. sulphonylureas, meglitinides
  • Patients with a known other cause for their increased liver enzyme levels such as viral hepatitis (B or C), autoimmune/chronic immune hepatitis, primary biliary cholangitis, metabolic and genetic hemochromatosis, Wilson's disease, or alpha-1 antitrypsin deficiency

Lab values

  • Subjects with platelets \<35 x 109/L and INR \> 2.0

Other

  • Pregnancy
  • Active substance abuse
  • Significant alcohol consumption ( \>20 g/day in women, \>30 g/day in men)
  • Weight \> 400 lbs, BMI \> 50 kg/m2.
  • Contraindications to obtaining a liver biopsy
  • Subjects with pre-existing abdominal pain will be excluded (because of the potential confusion with pain related to the procedure).
  • Subjects who are intolerant to PPIs
  • ASA Class 4 or 5
  • Child Pugh classification C
  • Contraindications to obtaining a liver biopsy (NASH cohort)

Who the study is looking for

  • Male or Female, aged 22 years or older.
  • Willing, able and mentally competent to provide written informed consent and willing to comply with all study procedures and be available for the duration of the study
  • BMI \>35 kg/m2
  • Adequate hematological, hepatic and renal function as follows:
    • Hematological: Hematological: If the bariatric embolization procedure is being performed by femoral access: platelets \> 50 x 109/L, INR \<1.5. If the bariatric embolization procedure is being performed by radial access: platelets \>35 x 109/L and INR \<1.5 OR platelets \>50 x 109/L and INR between 1.5 and 2."
    • Hepatic : Total bilirubin \<3 mg/dL
    • Renal: Estimated GFR \> 60ml/min.1.73m2
  • If Center for Epidemiological Studies Depression (CESD) score \> or =16 AND is in care of behavior health specialist who has indicated patient has adequate coping mechanisms to undergo procedure and does not foresee mental health as barrier to participation in study.
  • Elevated alanine or aspartate aminotransferase values (ALT \>41 or AST\>34 U/L).
  • Liver biopsy showing evidence of NASH in the past 12 months.
  • No evidence of another form of liver disease.
  • Patients diagnosed with NASH and have evidence of failing other methods of weight loss through diet, exercise and behavior modification.

Age in the registry: 22 years to 65 years · Sex: All · Accepts healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Saint Louis University
Coordinator of this site? Confirm its status
St LouisUnited StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.