- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02887573
Free-residue Nutrients for the Bowel Preparation of Colon Capsule Endoscopy
Study Overview
Status
Conditions
Detailed Description
Objective: In this study, a new bowel preparation regime of the colon capsule is used.This regime combines free-residue nutrients and polyethylene glycol (PEG) to achieve a better preparation quality.
Methods: Participants who underwent a diagnostic colonoscopy examination that demonstrated a colorectal polyps that required endoscopic treatment will be recruited to patients in the study. The first 32 participants receive a traditional low fiber diet two days before the test.Then the patients will take 2L polyethylene glycol (PEG) at 21:00-23:00 before the test day and 2L PEG at 05:00-07:00 on the test day for bowel preparation. The subsequent 30 participants receive two-days free-residue nutrients without other diet before the test.Then the patients will take 2L PEG at 05:00-07:00 on the examination day for bowel preparation. Then they will take 5mg mosapride citrate at 8:00 and ingest the colon capsule at 8:30.0.75L and 0.50L PEG are administered as boosters.And the therapeutic endoscopy will be given on the following day.Before the therapeutic colonoscopy, the participants will take 2L PEG. The colon capsule results will be reviewed by two experienced endoscopists who are blinded to first endoscopy results.
Study Type
Enrollment (Anticipated)
Phase
- Phase 4
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- 18-80 years of age.
- underwent a diagnostic OC that demonstrated colorectal polyps that required endoscopic treatment.
Exclusion Criteria:
- dysphagia/swallowing disorder
- prior major abdominal surgery of the gastrointestinal tract, known or suspected bowel obstruction
- cardiac pacemaker/implanted electromedical device
- pregnant or nursing women
- any allergy or contraindication to the drugs used in the study.
- refused to sign a informed consent.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Other
- Allocation: Non-Randomized
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Free-residue nutrients+PEG
Diet: Free-residue nutrients Free-residue nutrient will be given when the patients are hungry before the two days of the capsule day.There are no other diet in this arm. Drug: PEG 2L PEG are used at 05:00-07:00 the morning of the test. Drug: Mosapride citrate The patients will take 5mg mosapride citrate at 8:00. Drug:PEG 0.75L and 0.50L PEG are administered as boosters for patients. Procedure: Colon capsule endoscopy The colon capsule will be ingested at 08:30 the day of the test.The images will be reviewed by two experienced endoscopists. Procedure: Colonoscopy On the following day of the test.All participants will undergo therapeutic colonoscopy. |
This trial evaluated the efficiency of free-residue nutrients for the bowel prepartion of CCE.
In the study,all patients should undergo two colonoscopies.The first is for examinations and the second for therapy.
2L PEG are laxatives for experiment group.
Other Names:
These PEG are for boosters.
All patients will take 0.75L and 0.5L PEG for two boosters.
Other Names:
5mg mosapride citrate are used to promote gastric motivity.
|
|
Experimental: Low fiber diet+PEG
Diet: Low fiber diet Before the two days of the capsule day,when the patients hungry,low fiber diet wiil be given. Drug: PEG 4L PEG are used at 21:00-23:00 the night before the test and 05:00-07:00 the morning of the test. Drug: Mosapride citrate The patients will take 5mg mosapride citrate at 8:00. Drug:PEG 0.75L and 0.50L PEG are administered as boosters for patients. Procedure: Colon capsule endoscopy The colon capsule will be ingested at 08:30 the day of the test.The images will be reviewed by two experienced endoscopists. Procedure: Colonoscopy On the following day of the test,All participants will undergo therapeutic colonoscopy. |
In the study,all patients should undergo two colonoscopies.The first is for examinations and the second for therapy.
These PEG are for boosters.
All patients will take 0.75L and 0.5L PEG for two boosters.
Other Names:
5mg mosapride citrate are used to promote gastric motivity.
Low fiber diet often used in the bowel prepartion of CCE.
In this study, it is the control group.
4L PEG are laxatives in the control group.
Other Names:
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Bowel Cleansing Level of Two Different Bowel Preparation Methods
Time Frame: an expected average of 1 months from study procedure
|
The first 32 patients adopted a low fiber diet two days before the CCE procedure.
Bowel preparation included the ingestion of 2L polyethyleneglycol in the evening before test day and 2L PEG in the morning on the test day.
The subsequent 30 patients were received free-residue Nutrients。Then they ingested 2L PEG between 5:00 and 7.00 am of the examination day.
The capsule was scheduled at 8:30 am.
When the capsule reached the small bowel, 0.75L PEG was used as first booster.
If the capsule had not been excreted 3 hours later, the patients was received 0.5L PEG.
|
an expected average of 1 months from study procedure
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Accuracy parameters:assessment the yield of detection of polyps ≥6mm and ≥10mm;
Time Frame: an expected average of 1 months from study procedure
|
an expected average of 1 months from study procedure
|
|
|
The gastrointestinal tract transit times and the colonic transit times between two different bowel preparation methods for CCE;
Time Frame: an expected average of 1 months from study procedure
|
The gastrointestinal tract transit time was defined as the time from initial ingestion to capsule excretion.
The colon transit time defined as first capsule image of the cecum to capsule excretion.
|
an expected average of 1 months from study procedure
|
|
Colon capsule excretion rate between two different bowel preparation methods;
Time Frame: an expected average of 1 months from study procedure
|
an expected average of 1 months from study procedure
|
|
|
Adverse events between two different bowel preparation methods.
Time Frame: the PillCam procedure day
|
the PillCam procedure day
|
Collaborators and Investigators
Sponsor
Investigators
- Study Director: Wu kaichun, PhD, Xijing Hospital of Digestive Diseases
Study record dates
Study Major Dates
Study Start
Primary Completion (Anticipated)
Study Completion (Anticipated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- XijingHDD
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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