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临床试验/NCT03503162
NCT03503162已完成不适用

Evaluation of the Bowel Cleansing in Hospitalized Patients Using Pure-Vu System

Motus GI Medical Technologies Ltd1 个研究点 分布在 1 个国家目标入组 95 人开始时间: 2018年5月17日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
95
试验地点
1
主要终点
The Rate of Adequate Cleansing Level Before and After the Use of the Pure-Vu System

研究概览

简要总结

The aim of this study is to evaluate the potential improvement in colonoscopy procedure's outcomes when using the Pure-Vu System in hospitalized patients who are indicated for colonoscopy procedure.

详细描述

This multi-center, prospective, single arm study will include up to 100 patients (20-40 patients per site), aimed at evaluating the performance of the Pure-Vu System in cleansing hospitalized patients' colon who are indicated for standard colonoscopy procedure.

Subjects will be enrolled at up to 4 clinical sites in the United States and Europe. Subjects who meet the eligibility criteria will be prescribed a standard bowel preparation bowel preparation regimen including diet restrictions and oral bowel preparation.

Following the bowel preparation, the patient will undergo colonoscopy with the Pure-Vu system.

In case of inadequate bowel preparation, as per the nurse report and / or BBPS < 2, in at least one of the colon segments, prior Pure-Vu use, the physician will complete a questionnaire on the patient's management standard of care assuming the absence of Pure-Vu.

Follow-up will be conducted at 48 hours (± 48 hours) post procedure.

研究设计

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

入排标准

年龄范围
22 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •Hospitalized patients who are indicated for a screening, diagnostic, surveillance or therapeutic colonoscopy
  • •Patients' age > 22 years
  • •Patient has signed the informed consent

排除标准

  • •Patients with known Inflammatory Bowel Disease and / or active Colitis
  • •Patients with active diverticulitis
  • •Patients with known or detected (during colonoscopy) bowel obstruction
  • •Patients with BMI ≤ 18
  • •Patients with ascites Child Pugh C
  • •Patients who are 30 days post-transplant
  • •Patients treated with Peritoneal dialysis
  • •Patients under active IV inotropic medications
  • •Patients with LVAD
  • •Patients who have active anticoagulant medications (excluding aspirin) or dual antiplatelet therapy in their system prior to the procedure. (Note: to avoid exclusion therapy should be discontinued 48 hours or greater prior to the procedure based on discretion of physician)
  • •Subjects with known coagulation disorder (INR ≥ 2 or platelets <50,000)
  • •Subjects with hemodynamic instability.
  • •Pregnancy (as stated by patient) or breast feeding
  • •Subjects with altered mental status/inability to provide informed consent
  • •Patients who have participated in another interventional clinical study in the last 2 months

研究组 & 干预措施

Colonoscopy with Pure-Vu System

Experimental

Standard colonoscopy procedure with Pure-Vu System

干预措施: Pure-Vu System (Device)

结局指标

主要结局

The Rate of Adequate Cleansing Level Before and After the Use of the Pure-Vu System

时间窗: up to 2 hours

The rate of adequate cleansing level in each colon segment before and after use of Pure-Vu will be evaluated using the Boston Bowel Preparation Scale (BBPS). Segment score of 0-3 given to each of the 3 segments of the colon (Left side, Transverse and right side) summed for the maximum score of 9 (0= dirtiest and 9= pristine). An adequate cleansing procedure will be considered when all the colon segments will be graded as 2 or above.

次要结局

未报告次要终点

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (1)

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