A Single-arm, Observational, Post-marketing Study to Evaluate the Effects of the A.M.I. Protector Adjustable Gastric Band on Weight Loss, Co-morbidities, Adverse Events and Other Clinical Characteristics.
试验速览
- 阶段
- 不适用
- 发起方
- 入组人数
- 200
- 试验地点
- 1
- 主要终点
- Percentage excess weight loss (%EWL)
研究概览
简要总结
The laparoscopic adjustable gastric band (LAGB) is a safe and effective surgical intervention for chronically obese patients who have exhausted all non-surgical weight loss treatments. Numerous published studies have confirmed both the safety and efficacy of the LAGB and its beneficial impact on obesity-associated conditions, such as type 2 diabetes, joint and back pain and hypertension. The A.M.I. Protector Band is a modification of an existing gastric band (the A.M.I. Soft Gastric Band) which has been in use since 2001 and which has been shown to be both safe and effective. The specific design modification is in the form of a section of mesh, which provides support to the gastric pouch and which further restricts food portion sizes. The expectation is that this will deliver optimal weight loss whilst having the maximum possible impact on obesity-associated conditions such as type 2 diabetes and hypertension. In the longer term, there is also the possibility that the Protector Band will reduce the incidence of band complications such as slippage and dilatation (or stretching) of the gastric pouch. In this study we will recruit approximately 200 patients who will then undergo surgical implantation of the A.M.I. Protector Band. The study participants will then be followed for a period of 3-years, during which time we will record weight loss, changes in co-morbid conditions such as diabetes and the incidence of band complications, including slippage and pouch dilatation.
详细描述
Where patients express an interest in the A.M.I. Protector Band, they will be given a Patient Information Sheet which will form the basis of a discussion with the attending physician. Patients opting for the Protector Band will be told that their anonymised clinical data will be stored in a secure database and used for research purposes. They will also be required to attend for regular follow-up (see below) for a period of three years after implantation.
Following this initial consultation, a minimum period of 2-weeks will be required before the patient is listed for surgery. This will provide a suitable period during which the patient can consider the options and seek clarification on any points about which they are unclear.
In the case of the A.M.I. Protector Band the surgery will be performed in two locations:
- Spire Hospital Parkway (Birmingham)
- Spire Hospital Manchester
All band procedures will be performed by one of two surgeons; Mr. Paul Super and Prof. Franco Favretti according to a standard protocol.
研究设计
- 研究类型
- Observational
- 观察模型
- Cohort
- 时间视角
- Prospective
入排标准
- 年龄范围
- 18 Years 至 70 Years(Adult, Older Adult)
- 性别
- All
- 接受健康志愿者
- 是
入选标准
- •obese subjects with BMI >30kg/m2 with one or more co-morbidities
- •Obese subjects with BMI >40kg/m2 with or without co-morbidities
排除标准
- •previous history of drug abuse
- •history of bleeding disorders
- •On long-term steroid therapy
- •Pregnancy
- •Previous gastric surgery
- •Chronic lung disease
- •history of psychotic disease
- •Inflammatory bowel disease
- •Unstable angina or dysrhythmia
- •liver cirrhosis
- •Autoimmune disease (SLE etc)
结局指标
主要结局
Percentage excess weight loss (%EWL)
时间窗: 3 years
次要结局
- Impact of weight loss on co-morbidities such as type 2 diabetes, hypertension etc(3-years)
- Incidence of band-related complications such as band slippage; erosion; port/tubing complications; port/band infection; pouch dilatation(3 years)
