Clinical Study of Bowel Preparation Before Colonoscopy (NCT06091735) | Clinical Trial Compass
CompletedNot Applicable
Clinical Study of Bowel Preparation Before Colonoscopy
China444 participantsStarted 2023-08-01
Plain-language summary
This study was a single-center, randomized controlled clinical study. Subjects meeting the inclusion criteria will be randomly assigned to magnesium sodium potassium sulfate oral concentrated solution group, magnesium sodium potassium sulfate oral concentrated solution + linaclotide group, PEG group in equal proportion.
Who can participate
Age range
18 Years – 80 Years
Sex
ALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion Criteria:
* Signed written informed consent;
* Age 18-80 years old, gender is not limited;
* The subjects could follow the follow-up plan, objectively describe the symptoms, and cooperate with the completion of the scale;
* Non-lactating pregnant women and no pregnancy plan during the test;
* Do not participate in any clinical trials for 3 months before and during the trial;
* Participate voluntarily and sign informed consent.
Exclusion Criteria:
* NYHA cardiac function grade III or IV;
* Unstable angina pectoris in the convalescence period of acute myocardial infarction or in the near future;
* have serious liver and kidney function diseases;
* Suspected gastrointestinal obstruction or gastrointestinal perforation;
* Pregnant or lactating women;
* Mental illness or physical dysfunction can not cooperate with the examination;
* People who are allergic to intestinal preparation drugs.
* Patients who did not undergo colonoscopy after bowel clearing due to their own reasons;
* Patients who can not tolerate general colonoscopy and terminate the examination;
* Patients who requested withdrawal from the study.
Questions worth asking your doctor
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
Questions for the trial coordinator
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.