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临床试验/NCT05379491
NCT05379491已完成不适用

An Efficacy and Safety Evaluation of Linaclotide in Bowel Preparation by Patients at High Risk of Inadequate Bowel Preparation: a Multicenter, Randomized, Double-Blind, Controlled Clinical Trial

Zhiguo Liu8 个研究点 分布在 1 个国家目标入组 720 人开始时间: 2022年8月1日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
720
试验地点
8
主要终点
Bowel preparation adequate rate

研究概览

简要总结

The purpose of this study is to compare the colon cleansing quality of linaclotide versus control in adult patients at high risk of inadequate bowel preparation: one group will receive polyethylene glycol solution (PEG) split dose (1 L + 2 L) plus linaclotide and the other group PEG (1 L + 2 L) plus placebo before colonoscopy.

详细描述

The objective of this trial is to compare the colon cleanliness achieved with PEG split dose (1 L + 2 L) + linaclotide versus PEG split dose (1 L + 2 L) + placebo for patients scheduled for a colonoscopy at high risk of inadequate bowel preparation. The target patients are those with constipation, poor bowel preparation history, history of abdominal/pelvic surgery, comorbidity (diabetes, Parkinson's disease, stroke, or history of spinal cord injury), BMI > 25 kg/m2, age > 70, tricyclic antidepressants usage, or opioid usage, as defined by the latest version of Bowel Preparation Guidelines.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Supportive Care
盲法
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

盲法说明

A randomized grouping sequence by block randomization with a block size of 4 is generated using a web-based service. Linaclotide or placebo is allocated according to the sequence and labelled in numerial order (1 - 720) without labelling the allocation information. Therefore, patients, endoscopists, and other investigators at each center will be unaware of the drug allocation.

入排标准

年龄范围
18 Years 至 75 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • scheduled for colonoscopy
  • meet any of the followings: functional constipation according to Rome IV criteria, poor bowel preparation history, BMI > 25 kg/m2, age > 70, history of abdominal/pelvic surgery, comorbidity (diabetes, Parkinson's disease, stroke, or history of spinal cord injury), antidepressant usage, opioid usage
  • willing to provide informed consent

排除标准

  • unable to cooperate with questionnaires
  • uncontrolled hypertension (systolic .170 mm Hg and diastolic.100mmHg)
  • pregnancy or lactation
  • toxic colitis, or megacolon
  • allergy to preparation components
  • active inflammatory bowel disease
  • clinically significant electrolyte abnormalities
  • a history of severe renal, liver, or cardiac insufficiency
  • has already been enrolled in the study
  • gastrointestinal obstruction
  • obvious gastroparesis or gastric retention
  • bowel perforation
  • polyp syndrome
  • history of colectomy
  • any other condition that is inappropriate for enrollment as judged by the investigator.

研究组 & 干预措施

3 L PEG + Linaclotide

Active Comparator

Bowel preparation for colonoscopy was performed with 3 L polyethylene glycol solution combined with 2-day linaclotide.

干预措施: 3 L PEG + linaclotide (Drug)

3 L PEG + Placebo

Placebo Comparator

Bowel preparation for colonoscopy was performed with 3 L polyethylene glycol solution combined with 2-day placebo.

干预措施: 3 L PEG + placebo (Drug)

结局指标

主要结局

Bowel preparation adequate rate

时间窗: 48 hours

The rate of participants with all colon segment scores (proximal colon, transverse colon, distal colon) are ≥ 2 according to Boston Bowel Preparation Scale.

Number of adenomas per patient

时间窗: 48 hours

If there is no significant difference in the first primary outcome between the two groups, compare the average number of adenomas per patient detected by colonoscopy.

次要结局

  • Subject willingness to repeat the preparation(1 Day of colonoscopy)
  • Tolerance to bowel preparation(1 Day of colonoscopy)
  • Tolerance to colonoscopy(1 Day of colonoscopy)
  • Average number of polyps per patient(1 Day of colonoscopy)
  • Average number of adenomas per patient(1 Day of colonoscopy)
  • Withdrawal time(1Day of colonoscopy)
  • Cecal intubation rate for colonoscopies(1 Day of colonoscopy)

研究者

发起方
Zhiguo Liu
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

Zhiguo Liu

Associate Professor

Xijing Hospital of Digestive Diseases

研究点 (8)

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