ISRCTN70400953已完成未知
Prospective randomized trial to compare the clinical efficiency (Adenoma Detection Rate) of G-EYE™ HD Colonoscopy with Standard HD Colonoscopy
适应症
试验速览
- 阶段
- 未知
- 状态
- 已完成
- 入组人数
- 1,000
研究概览
简要总结
2019 results in: https://www.ncbi.nlm.nih.gov/pubmed/30273591 (added 10/04/2019)
研究设计
- 研究类型
- Interventional
入排标准
- 性别
- All
入选标准
- •1. Patients over 50
- •2. Referred to colonoscopy for screening, following positive Fecal Occult Blood Test (FOBT) testing, change of bowel habits or for surveillance colonoscopy (history of adenoma resection)
- •3. The patient must understand and provide written consent for the procedure
排除标准
- •1. Subjects with inflammatory bowel disease
- •2. Subjects with a personal history of polyposis syndrome
- •3. Subjects with suspected chronic stricture potentially precluding complete colonoscopy
- •4. Subjects with diverticulitis or toxic megacolon
- •5. Subjects with a history of radiation therapy to abdomen or pelvis
- •6. Pregnant or lactating female subjects
- •7. Subjects who are currently enrolled in another clinical investigation.
- •8. Subjects with current oral or parenteral use of anticoagulants
- •9. Subjects with recent (within the last 3 mounts) coronary ischemia or CVA (stroke)
- •10. Any patient condition deemed too risky for the study by the investigator
- •11. Previous colonic surgery (except for appendectomy)
研究者
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