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Blocking stomach blood flow to fight obesity: a new approach?

NCT ID NCT04207424

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled This study
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

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 However, the study was withdrawn before any participants were enrolled, so its safety and effectiveness remain unknown.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The study was withdrawn before enrolling anyone, so no results are available.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

Mar 2020

Expected to finish

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

18 to 71 years

Sex

Anyone

Healthy volunteers

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

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

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