Free-residue Nutrients for the Bowel Preparation of Colon Capsule Endoscopy

February 4, 2017 updated by: Kaichun Wu
Colon capsule endoscopy(CCE) is a new diagnostic method of colonic lesions.It has advantages of no requirement for sedation and air insufflation.The bowel preparation has a closely relationship with yield of diagnosing diseases.Bowel preparation of CCE is not only to clean the colon but also to promote capsule propulsion.Now there is not an optimal method for CCE.

Study Overview

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

Interventional

Enrollment (Anticipated)

62

Phase

  • Phase 4

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

14 years to 76 years (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • 18-80 years of age.
  • underwent a diagnostic OC that demonstrated colorectal polyps that required endoscopic treatment.

Exclusion Criteria:

  1. dysphagia/swallowing disorder
  2. prior major abdominal surgery of the gastrointestinal tract, known or suspected bowel obstruction
  3. cardiac pacemaker/implanted electromedical device
  4. pregnant or nursing women
  5. any allergy or contraindication to the drugs used in the study.
  6. refused to sign a informed consent.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

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:
  • polyethylene glycol
These PEG are for boosters. All patients will take 0.75L and 0.5L PEG for two boosters.
Other Names:
  • polyethylene glycol
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:
  • polyethylene glycol
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:
  • polyethylene glycol

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

This is where you will find people and organizations involved with this study.

Sponsor

Investigators

  • Study Director: Wu kaichun, PhD, Xijing Hospital of Digestive Diseases

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start

January 1, 2014

Primary Completion (Anticipated)

July 1, 2017

Study Completion (Anticipated)

July 1, 2017

Study Registration Dates

First Submitted

August 20, 2016

First Submitted That Met QC Criteria

August 29, 2016

First Posted (Estimate)

September 2, 2016

Study Record Updates

Last Update Posted (Estimate)

February 7, 2017

Last Update Submitted That Met QC Criteria

February 4, 2017

Last Verified

February 1, 2017

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

Undecided

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.

Clinical Trials on Colorectal Polyps

Clinical Trials on Free-residue nutrients

Subscribe