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临床试验/NCT00580502
NCT00580502已完成2 期

A Prospective Study to Evaluate the Safety and Efficacy of LAP-BAND® Adjustable Gastric Band (LAGB®) Operations for Patients With BMI Between 30-40 kg/m2 With Co-morbidities

NYU Langone Health0 个研究点目标入组 50 人开始时间: 2004年3月1日最近更新:
适应症
干预措施

试验速览

阶段
2 期
状态
已完成
入组人数
50
主要终点
To Determine Percent of Excess Weight Loss (%EWL) After Laparoscopic Adjustable Gastric Banding Surgery

研究概览

简要总结

This study is to evaluate the safety and efficacy of Gastric Banding for patients with body mass index (BMI) between 30-40 kg/m2 with medical conditions related to obesity.

详细描述

TITLE OF STUDY:A prospective study to evaluate the safety and efficacy of LAP-BAND® Adjustable Gastric Band (LAGB®) operations for patients with BMI between 30-40 kg/m2 with co-morbidities

CLINICAL PHASE: Phase III new indication for use of the device not yet approved by FDA

STUDY OBJECTIVES

  • To determine the safety and efficacy of the LAP-BAND® Adjustable Gastric Band (LAGB®) for patients with BMI between 30-40 kg/m2 with co-morbidities
  • To determine long-term effects on patients' co-morbidities

STUDY VARIABLES: Morbidity & mortality, percent of excess weight loss, nutritional status, improvement of pre-operative co-morbidities, weight loss maintained, and quality of life evaluation

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 60 Years(Adult)
性别
All
接受健康志愿者
否

入选标准

  • •Be at least 18 and equal to or less than 60 years of age.
  • •BMI of at least 30 and maximum BMI of 40 with co-morbidities
  • •Willingness to comply with dietary restrictions required by the protocol
  • •History of obesity for at least 5 years
  • •History of at least 6 months of documented failures with traditional non-surgical weight loss methods
  • •Willingness to follow protocol requirements
  • •If female with childbearing potential, using an appropriate form of contraception

排除标准

  • •Age less than 18, age greater than 60
  • •Pregnancy
  • •History of major depressive disorder or psychosis
  • •Previous bariatric surgery or previous gastric surgery
  • •Presence of achalasia
  • •Presence of portal hypertension, cirrhosis, and/or varices
  • •Patient with inflammatory disease of the gastrointestinal tract such as Crohn's Disease
  • •Patients with autoimmune connective tissue disorders
  • •Patients with acute abdominal infections
  • •Any condition that, in the judgment of the investigator, would place a subject at undue risk, or potentially compromise the results or interpretation of the study

研究组 & 干预措施

LAGB for low BMI patients

Experimental

the LAP-BAND® Adjustable Gastric Band (LAGB®) for patients with BMI between 30-40 kg/m2 with co-morbidities

干预措施: LAP-BAND® Adjustable Gastric Band (LAGB®) (Device)

结局指标

主要结局

To Determine Percent of Excess Weight Loss (%EWL) After Laparoscopic Adjustable Gastric Banding Surgery

时间窗: 5 years

Change in weight from baseline at 5 years by calculating the percentage of the weight loss from the total excess weight.

次要结局

  • Level of LDL (Bad Cholesterol) After Laparoscopic Adjustable Gastric Band Surgery(5 years)
  • Level of Triglycerides (Bad Cholesterol) After Laparoscopic Adjustable Gastric Band Surgery(5 years)
  • Level of HbA1c (Blood Test for Diabetes) After Laparoscopic Adjustable Gastric Band Surgery(5 years)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Heekoung A Youn

Research coordinator

NYU Langone Health

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