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临床试验/NCT02165124
NCT02165124已完成不适用

Bariatric Embolization of Arteries for the Treatment of Obesity

Johns Hopkins University2 个研究点 分布在 1 个国家目标入组 20 人开始时间: 2014年6月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
20
试验地点
2
主要终点
Percent Weight Change

研究概览

简要总结

The purpose of this study is evaluate the safety and effectiveness of bariatric embolization as a minimally-invasive image-guided procedure for morbid obesity. In this procedure, specific blood vessels to the stomach are blocked in order to suppress some of the body's signals for feeling hungry, leading to weight loss.

Morbid obesity is currently treated with diet and exercise, medications, and surgery. This study is designed to help treat obesity using a minimally invasive, non-surgical, angiographic (through the blood vessel) approach. This procedure is similar to a common procedure used to treat bleeding within the stomach. This version of the procedure has been named "bariatric embolization".

Although there are over 40 hormones that limit food intake, there is only one hormone, ghrelin that has been shown to stimulate (prompt) food intake. In obese patients, eating fails to suppress ghrelin levels, which is believed to prevent feeling full after a meal and to lead to overeating. Due to the strong hunger craving effects of ghrelin, this hormone has been a target for the treatment of obesity and weight loss. More recently, ghrelin has been shown to have a significant role in the long-term effect of weight loss in bariatric (obesity) surgery where ghrelin levels are shown to be much lower when compared to untreated patients.

Recent data collected in animals in has shown that blocking blood vessels to a particular portion of the stomach (bariatric embolization) can temporarily decrease levels of the appetite inducing hormone ghrelin, and decrease short-term weight gain. In a study of 5 people, there was a decrease in ghrelin levels and weight loss in the first month after the procedure, but there is no information about the effects of the procedure over longer periods of time.

The investigator hopes to learn if bariatric embolization results in safe and effective weight loss in people who are morbidly obese.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 75 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Willing, able and mentally competent to provide written informed consent.
  • Body mass index (BMI) between 40-
  • Residence within 25 miles of the enrolling institution
  • Vascular anatomy (including celiac, hepatic, and gastric arteries) that in the opinion of the interventional radiologist amenable to Bariatric Embolization, as assessed on 3D CT angiography.
  • Suitable for protocol therapy as determined by the interventional radiology Investigator.
  • Adequate hematological, hepatic and renal function as follows:
  • Hematological Neutrophils > 1.5 x 109/L Platelets > 100 x 109/L International Normalized Ratio (INR) <1.5
  • Hepatic Bilirubin ≤ 2.0 mg/dL Albumin ≥ 2.5 g/L
  • Renal Estimated Glomerular Filtration Rate (GFR) > 60ml/min.1.73m2
  • Aged 18 years or older.

排除标准

  • Prior history of gastric pancreatic, hepatic, and/or splenic surgery
  • Prior radiation to the upper abdomen
  • Prior embolization to the stomach, spleen or liver
  • Portal venous hypertension
  • Prior or current history of peptic ulcer disease
  • Hiatal Hernia
  • Significant risk factors for peptic ulcer disease including daily NSAID use and smoking.
  • Active H. Pylori infection
  • Weight greater than 400 pound
  • Known aortic pathology such as aneurysm or dissection renal insufficiency as evidenced by an estimated glomerular filtration rate of < 60 milliliters per minute
  • Major comorbidity such as cancer, significant cardiovascular disease, diabetes, or peripheral arterial disease.
  • Complicated arterial anatomic variants including left gastric artery arising from the aorta, and/or hepatic arterial supply via a replaced or accessory left hepatic artery arising from the left gastric artery.
  • Preexisting chronic abdominal pain
  • Positive stool occult study
  • Abnormal Endoscopy
  • Abnormal Nuclear Gastric Motility examination
  • American Society of Anaesthesiologists (ASA) Class 4 or 5 (very high risk surgical candidates: class 4= incapacitating disease that is a constant threat to life) at the time of screening for enrollment into the study will be excluded from participation. This exclusion criterion exists because of the possibility that surgical intervention will be needed if the study intervention subsequently leads to severe adverse effects.
  • History of Inflammatory Bowel Disease
  • Autoimmune disease
  • Known history of allergy to iodinated contrast media

结局指标

主要结局

Percent Weight Change

时间窗: 12 Months

This will be assessed by Percentage of excess weight loss (EWL). Percentage of excess weight loss is calculated by measuring the participants excess weight at baseline and then calculating the percentage of excess weight that was lost 12 months after surgery (for example if a participant has 100 pounds of excess weight prior to surgery and loses 30 pounds, their excess weight loss would be 30%).

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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