Phase II Study of Evaluation of the Safety and Effectiveness of Stomaphyx for Transoral Incisionless Reduction of the Enlarged Gastric Pouch and Stoma
试验速览
- 阶段
- 2 期
- 状态
- 已完成
- 入组人数
- 14
- 试验地点
- 2
- 主要终点
- Primary Outcome: Change in Body Weight
研究概览
简要总结
Executive Summary
Aims and Hypotheses of the Study:
The aim of the study will be to evaluate the safety, effectiveness and early outcome of the StomaphyX procedure for reducing the enlarged gastric pouch and stoma in post-bariatric patients. The study will test a hypothesis that the StomaphyX procedure will be effective in promoting the loss of regained weight, reducing the risk for comorbidities and improving patients' quality of life.
Type of Study: Prospective non-randomized Study Duration: 12 months Number of Patients: 20
Inclusion Criteria:
18-70 years of age, BMI ≥ 35, ≥ 2 years after primary Roux-en-Y gastric bypass with evidence of enlarged gastric pouch volume or enlarged stoma diameter of ≥ 20 mm via endoscopy or fluoroscopy. Pts also demonstrate a weight regain of 15% of excess body weight loss.
Exclusion Criteria:
Esophageal stricture, or any anatomic conditions that preclude passage of transoral endoluminal instruments, has another causal factor for weight regain other than stoma or pouch dilatation, portal hypertension, coagulation disorders or chronic use of anticoagulants, any active medical condition that would preclude the patient from completing the study or would result in an unreasonable risk to the patient.
Intervention Treatment: Creation of multiple full-thickness plications within the gastric pouch using the StomaphyX device (EndoGastric Solutions, Inc., Redmond, WA, USA)
Evaluation Criteria Primary Outcome: Change in body weight at 6 and 12 months Secondary Outcome: Gastric pouch volume assessment, stoma diameter determination, quality of life scores, waist circumference, co-morbidity resolution Effectiveness and Safety Assessment Clinical: Weight, height, waist circumference quality of life questionnaires (Impact of Weight QOL-Lite, Eating and Weight Patterns, Three-factor Eating, Emotional Eating Scale, GI QoL, GSRS and/or PGWB) Anatomical: Upper GI endoscopy, computed tomography or barium radiography Biochemical: Blood and urine tests (glucose, cholesterol, triglyceride, HDL, LDL, uric acid) Safety: Adverse events, complications, co-morbidities, hospital stay
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 70 Years（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Age 18-70 years
- •BMI 35 or greater with one or more comorbidities
- •At least 2 years post-Roux-en-Y gastric bypass surgery
- •At enrollment, has regained at least 15% of excess body weight loss
- •Enlarged Stoma Diameter
- •Enlarged gastric pouch
- •Completed successful nutritional screening and compliant with nutritional programs
- •Completed successful cardiopulmonary evaluation
- •Patient willing to cooperate with follow-up assessment tests
- •Signed informed consent
排除标准
- •Esophageal stricture or any anatomic conditions that preclude passage of transoral endoluminal instruments
- •Has another causal factor for weight regain other than stoma or pouch dilatation such as non compliant with nutritional and exercise programs
- •Portal hypertension
- •Coagulation disorders or chronic use of anticoagulants
- •Any active medical condition that would preclude the patient from completing the study or would result in an unreasonable risk to the patient
结局指标
主要结局
Primary Outcome: Change in Body Weight
时间窗: At 6 months comparing to baseline weight
Body weight changes at 6 months after StomaphyX procedure comparing to baseline weight.
次要结局
未报告次要终点
研究者
Shahzeer Karmali
BSc, MD, FRCSC
University of Alberta