Blocking stomach blood flow to fight obesity: a new approach?
NCT ID NCT04207424
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study planned to test a procedure called bariatric embolization for people with morbid obesity who cannot have standard weight-loss surgery. The procedure involves injecting tiny particles into blood vessels near the stomach to reduce blood flow, which may lower hunger hormones and help with weight loss. However, the study was withdrawn before any participants were enrolled, so its safety and effectiveness remain unknown.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Embolization of the gastro-epiploic arcade using polyvinyl-alcohol microparticles
- What this could lead to
- If it worked, this procedure could offer a less invasive option for weight loss in people who cannot have bariatric surgery.
- What could go wrong
- The study was withdrawn before enrolling anyone, so no results are available. The procedure carries risks like allergic reaction to contrast dye and potential complications from blocking blood vessels.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
-
Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Started
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Mar 2020
- Expected to finish
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May 2025
An estimate. End dates often move.
- Lead sponsor
-
Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 to 71 years
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Adult patient aged ≥18 and ≤ 71 years old * BMI ≥ 40 or BMI ≥ 35 in association with one of the following comorbidities: hypertension, type 2 diabetes, obstructive sleep apnea * Relative contraindication to bariatric surgery * Able to sign informed consent. Exclusion Criteria: General * Impossible or unwilling to attend follow-up visits. * Weight \> 250kg (weight limit of angiography table) * Confirmed allergy to intravenous contrast agents. * Pregnancy, breast feeding or willingness to conceive during the following year * Impossible to maintain dorsal decubitus during intervention * Life expectancy \< 1 year * Current enrollment in another clinical trial * Arterial anatomy rendering embolization very difficult or impossible (as evaluated by investigators) * Patient under the protection of justice * Patient under guardianship or trusteeship Gastro-intestinal * Pre-existing chronic abdominal pain * History of inflammatory bowel disease * History of gastroparesis * History of gastric surgery, gastric embolization or radiotherapy * History of peptic ulcer * Significant risk factors for peptic ulcer, including daily use of non-steroidal anti-inflammatory drugs, active smoking or active infection with Helicobacter pylori * Abnormal upper digestive endoscopy Hepatic * Cirrhosis * Portal venous hypertension * Bilirubin \> 2,0 mg/dL * Albumin \< 2,5 g/L Cardiovascular * Known aortic pathology i.e. aneurysm or dissection * Severe peripheral arterial disease Renal \- Renal failure, Creatinine Clearance \< 60ml/min/1,73 m2 Hematologic/Immunologic/Oncologic/Infectious * Acute or chronic infection * Active cancer * Auto-immune disease requiring immunosuppression * Neutrophil count \< 1,5 x 10 \^ 9/L * Platelet count \< 100 x 10 \^ 9/L Contraindication to contrast medium Visipaque solution for injection * Hypersensitivity to the active substance (Iodixanol) or to any of the excipients * History of immediate major or delayed skin reaction to the injection of the product * Decompensated heart failure * Thyrotoxicosis * Contraindication to the use of the embogold microsphere
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
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