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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

Status
Not yet recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02933554
Enrollment
8
Registered
2016-10-14
Start date
2025-12-31
Completion date
2027-06-30
Last updated
2025-07-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Body Weight, NAFLD, Nonalcoholic Fatty Liver Disease, Nonalcoholic Steatohepatitis, Obesity, Weight Loss

Keywords

bariatric surgery, minimally invasive, Embolization, NASH, ghrelin, gastric artery embolization

Brief summary

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.

Detailed description

Obesity:In adults, obesity is defined as a BMI of greater than 30 kg/m2. It is estimated that, by the year 2030, 38% of the world's adult population will be overweight and another 20% obese.An expert panel convened by the NIH stated that for the first time in history, the steadily improving worldwide life expectancy could level off or even decline, as the result of increasing obesity. NAFLD and NASH: The Problem: Obesity is a chronic disease that is strongly associated with a number of diseases with an increase in mortality and morbidity. Metabolic syndrome (obesity, diabetes mellitus, hyperlipidemia) has been established as risk factor for primary nonalcoholic fatty liver disease (NAFLD) .In the US, recent estimates suggest that NAFLD affects 30% of the general population, 90% of the morbidly obese . NAFLD can progress to nonalcoholic steatohepatitis (NASH) in up to 25% . Of patients with NASH progression of fibrosis is seen in 26-37% and progressing to cirrhosis in 9-25 % . NASH cirrhosis can result in liver failure, portal hypertension, and hepatocellular carcinoma(HCC) . Current options in management of NASH: The goal of managing NASH is to eliminate risk factors and preventing fibrosis by treating metabolic syndrome, primarily obesity \[10\]. Although dietary modification and exercise can achieve weight loss, this is difficult to sustain . Very few effective medical therapies are available, and are associated with adverse effects. Although weight loss after bariatric surgery has demonstrated histological improvement in NASH, a recent Cochrane review concluded that there is insufficient data to determine if bariatric surgery is an effective treatment. Also high mortality rates are seen post-bariatric surgery. Thus a safe and effective minimally invasive option is needed. Based on currently available data, Left gastric artery embolization (LGAE) appears effective in inducing weight loss of about 10.5% in 3-6 months, with a high safety profile. In patients with NAFLD, a 3-5% weight loss is thought to improve steatosis, 7- 10% may be needed to improve necroinflammation. Thus, LGAE has the potential to reverse the histology of NASH to prevent progression to cirrhosis, HCC and its sequale.

Interventions

Via a radial artery in the wrist or the femoral artery in the groin, arterial access will be obtained.Under live X-ray monitoring and using contrast, a catheter will be advanced into the artery of the stomach (left gastric artery). A CT scan will be performed on the X ray table to confirm the placement of catheter. Once this is confirmed small micro spherical particles (Embopheres Microspheres) will be injected though the catheter to occlude the artery and cut off blood supply to the stomach. Once the procedure is complete, in case of wrist access compression will be achieved with a band; in case of groin access a closure device will be used to plug the site of entry.

Sponsors

Keith Pereira, MD:
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
22 Years to 65 Years
Healthy volunteers
Yes

Inclusion criteria

1. Male or Female, aged 22 years or older. 2. 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 3. BMI \>35 kg/m2 4. Adequate hematological, hepatic and renal function as follows: 1. 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. 2. Hepatic : Total bilirubin \<3 mg/dL 3. Renal: Estimated GFR \> 60ml/min.1.73m2 5. 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. 6. Elevated alanine or aspartate aminotransferase values (ALT \>41 or AST\>34 U/L). 7. Liver biopsy showing evidence of NASH in the past 12 months. 8. No evidence of another form of liver disease. 9. Patients diagnosed with NASH and have evidence of failing other methods of weight loss through diet, exercise and behavior modification.

Exclusion criteria

1. Pregnancy 2. Active substance abuse 3. 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. \[If Center for Epidemiological Studies Depression (CESD) score \> or =16 AND is in care of behavior health specialist who has indicated patient has adequate coping mechanisms to undergo procedure and does not foresee mental health as barrier to participation in study.\] 4. Significant alcohol consumption ( \>20 g/day in women, \>30 g/day in men) 5. Weight \> 400 lbs, BMI \> 50 kg/m2. 6. Contraindications to obtaining a liver biopsy 7. Subjects with pre-existing abdominal pain will be excluded (because of the potential confusion with pain related to the procedure). 8. Subjects who are intolerant to PPIs 9. Subjects requiring any anticoagulant medications should be excluded if radial access cannot be obtained. 10. Subjects with platelets \<35 x 109/L and INR \> 2.0 11. 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). 12. 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

Design outcomes

Primary

MeasureTime frameDescription
Weight12 monthsTotal body Weight loss \> 10 % in 12 months

Secondary

MeasureTime frameDescription
Clinical parameter-Blood pressure12 monthsImprovement in blood pressure measured in mmHg
Laboratory parameter-Ghrelin and other serum obesity hormones(Leptin, GLP-1, PYY)12 monthsReduction in serum Ghrelin and other serum obesity hormones(Leptin, GLP-1, PYY) measured in pg/mL
Laboratory parameter-serum glucose12 monthsReduction in serum glucose levels measured as mg/dL
Laboratory parameters- HbA1c12 monthsReduction in HbA1c measures as percentage(%)
Clinical parameter- Abdominal circumference12 monthsImprovement in abdominal circumference measured in centimeters (cm)
Number of patients with clinical adverse events12 monthsAdverse events like pain, ischemia
Results from endoscopy12 monthsPhotos and clinical reports analyzed
Change in inflammation, fibrosis, steatosis in liver histology12 monthsChange in liver histology between baseline and 12 months in liver histology
NAFLD activity score12 monthsChange in NAFLD Activity score (Kleiner) between baseline and 12 months in liver histology
Laboratory parameters-Lipid profile12 monthsImprovement in lipid profile measured as mg/dL

Countries

United States

Contacts

Primary ContactKeith Pereira, MD
keith.pereira@health.slu.edu314-268-5558

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026