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临床试验/NCT04592601
NCT04592601Unknown不适用

The S.L.I.M.M.S. Procedure for Severe Clinical Obesity

The N.E.W. Program2 个研究点 分布在 1 个国家目标入组 200 人开始时间: 2020年10月26日最近更新:
适应症
干预措施

试验速览

阶段
不适用
发起方
入组人数
200
试验地点
2
主要终点
Weight Loss

研究概览

简要总结

Assessment of Gastric Bypass combined with Vertical Sleeve Gastrectomy as primary treatment for patients with severe clinical obesity.

Average percentage of total weight loss and percentage excess weight loss will be computed at 6 months, one year and then annually. Comorbid conditions, quality of life measures, appetite and satiety measures and adverse events will be tracked.

详细描述

BACKGROUND

Metabolic Disease and Obesity

Obesity is one of the most common chronic diseases in America and is strongly associated with additional metabolic disorders, in particular hypertension, dyslipidemia and insulin resistance. The combination of obesity with this cluster of metabolic disorders increases risk for cardiovascular disease and is widely recognized by the term Metabolic Syndrome.

According to the Centers for Disease Control, in 2017-2018 the "prevalence of severe obesity among U.S. adults was 9.2%", the "age-adjusted prevalence of obesity in adults was 42.4%", and the prevalence of metabolic syndrome (MS) in the obese population is higher than 60%. The economic impact of metabolic syndrome is significant, with risk factors for MS shown to increase a person's annual healthcare costs by more than $2000.

Efforts to treat obesity and obesity-associated metabolic disease currently include medical management and surgical intervention. Success rates with surgical interventions exceed those of medical management but are dependent on patients making permanent changes in eating behaviors.

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 65 Years(Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •Be between 18 and 65 years of age
  • •Have a body mass index of equal to or above 35 kgs per m2
  • •Have identifiable obesity-related comorbidity; medical, physical or psycho-social
  • •A history of attempts at weight reduction within the past five-year period
  • •Ability to understand the non-surgical and surgical options for weight loss
  • •Understand the behavioral changes needed to maximize surgical weight loss success
  • •Agree to comply with recommended follow-up clinical assessments
  • •Agree to comply with lifelong nutritional supplementation

排除标准

  • •Lack of ability to understand weight loss options and requirements for long-term success with surgery
  • •Inability to understand and accept the risks and potential benefits
  • •Inability to understand and agree to the compliance requirements of the study
  • •Prior gastric surgery including all forms of bariatric surgical or endoscopic procedures
  • •A history of previous abdominal surgery which precludes gastric bypass
  • •Medical contra-indications to bariatric surgery
  • •Dementia, active psychosis, unstable psychiatric disease
  • •Concurrent experimental drug use
  • •Pregnancy or intending to conceive within 12 months or current breast-feeding
  • •Recreational drug use or excessive alcohol intake
  • •Use of drugs known to affect body composition
  • •Use of cytotoxic drugs

研究组 & 干预措施

S.L.I.M.M.S. Procedure

Experimental

Prospective collection of data on the safety and efficacy of the S.L.I.M.M.S. Procedure

干预措施: S.L.I.M.M.S. Procedure (Procedure)

结局指标

主要结局

Weight Loss

时间窗: 6 months, 12 months and 2 years

Primary efficacy variable is Weight Loss Weight loss will be measured as: 1. Pounds lost (pre-op weight - post-op weight) 2. Total Weight Loss, calculated as (Pre-op Weight-Current Weight) in pounds (lb) 3. Percent Excess Weight Loss, calculated as \[(Pre-op Weight - Ideal Body Weight)/Ideal Body Weight\] x 100. Ideal Body Weight calculated using the universal IBW formula.

次要结局

  • Metabolic Comorbidity(2 Years)
  • Changes in Quality of Life from baseline(2 Years)
  • Adverse Events(2 Years)

研究者

发起方
The N.E.W. Program
申办方类型
Other
责任方
Principal Investigator
主要研究者

BRIAN B. QUEBBEMANN, M.D., F.A.C.S.

Director

The N.E.W. Program

研究点 (2)

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