3-day vs. 1-day Low Residue Diet Influence in Colonoscopy Preparation and Patient Tolerability
Primary Purpose
Colon Disease, Colonic Neoplasms
Status
Completed
Phase
Not Applicable
Locations
Portugal
Study Type
Interventional
Intervention
3 day low residue diet prior to the colonoscopy
1 day low residue diet prior to the colonoscopy
Sponsored by
About this trial
This is an interventional diagnostic trial for Colon Disease focused on measuring Randomized controlled trial, Colonoscopy, Colon Disease, Low residue diet, Colon preparation
Eligibility Criteria
Inclusion Criteria:
- Consecutive series of patients scheduled for total colonoscopy
- Signed informed consent
Exclusion Criteria:
- inpatients
- sedation
- urgent procedures
- colonoscopies not intended to reach the caecum
- patient with previous partial colectomy.
Sites / Locations
- Portuguese Oncology Institute - Coimbra
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Placebo Comparator
Arm Label
3-day low residue diet
1-day low residue diet
Arm Description
Group A - 3 day low residue diet prior to the colonoscopy
Group B - 1 day low residue diet prior to the colonoscopy
Outcomes
Primary Outcome Measures
Score of mucosal visualization
Using Boston Bowel Preparation Scale during the exam
Secondary Outcome Measures
Patient assessment of diet protocol
Patient assessment, by written questionnaire, of tolerance and acceptance of diet protocol.
Polyp detection rate, location and configuration
One of the quality indicators for colonoscopy is polyp detection rate, which is defined as the percentage of colonoscopies with a detection of at least one polyp. At the same time the endoscopist will assign the colonic location of the polyp (ascendent, transverse, descendent).
(PDR to be presented as %; Location to be discriminated in the endoscopist report).
Adenoma Detection Rate
Adenoma detection rate (ADR) is the one of the strongest quality indicators for colonoscopy. This rate represents the percentage of colonoscopies with at least one adenoma identified. (to be presented as %)
Cecum intubation rate
Defined as colonoscopy quality indicator the photo documentation of cecum, in at least 95% of the colonoscopies. Photo documentation of the cecum is a mark for effective total colonoscopy. (to presented as %)
Withdrawal time
In a negative colonoscopy (no polyp identification) is defined that the withdrawal time should be at least 6 minutes for proper and safe colonic mucosa evaluation. (to be presented in minutes)
Full Information
NCT ID
NCT02955901
First Posted
October 25, 2016
Last Updated
July 13, 2019
Sponsor
Portuguese Oncology Institute, Coimbra
1. Study Identification
Unique Protocol Identification Number
NCT02955901
Brief Title
3-day vs. 1-day Low Residue Diet Influence in Colonoscopy Preparation and Patient Tolerability
Official Title
A 3-day Versus 1-day Low Residue Diet to Improve Colonoscopy Preparation Result and Patient Tolerability: A Prospective, Randomized, Single-blinded, Controlled Trial
Study Type
Interventional
2. Study Status
Record Verification Date
July 2019
Overall Recruitment Status
Completed
Study Start Date
January 1, 2017 (Actual)
Primary Completion Date
December 2018 (Actual)
Study Completion Date
May 2019 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Portuguese Oncology Institute, Coimbra
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
Colonoscopy is one of the most common methods for the diagnosis and treatment of lower gastrointestinal tract diseases and provides a unique opportunity to identify early neoplastic lesions.
Adequate bowel preparation is important for optimal colonoscopy. New bowel-cleansing regimens, study of patient-related risk factors to fail a proper preparation and diet adaptations have been studied recently.
A low residue diet is the standard in the day before the colonoscopy. Some endoscopists prescribe this dietary plan for a 3-day period prior to the exam, although no study compared the recommended 1-day versus 3-day diet regime, or the influence in bowel preparation results.
The aim of this project is to determine if the use of a 3-day low residue diet improves bowel preparations results and the influence in patient tolerability and adherence.
Detailed Description
a. Study type: prospective, randomized, single-blinded trial:
i. Prospective inclusion of ambulatory patients;
ii. Randomization by computer generated tables;
iii. Allocation concealment by sealed, opaque envelopes;
iv. Patient not blinded to diet;
v. Endoscopist blinded to the diet followed by each patient.
b. Patient selection: Consecutive series of patients scheduled for total colonoscopy; Exclusion criteria: inpatients, sedation, urgent procedures, colonoscopies not intended to reach the caecum, patient with previous partial colectomy.
c. Sample Size:
i. 412 individuals; 2 groups of 206 patients
ii. Primary goal: to achieve a reduction from 15 to 5% of inappropriate preparation result; The Boston Bowel Preparation Scale (BBPS) will be used as grading system. Inappropriate is defined as total BBPS < 6 or < 2 in any segment. The chosen scale is the most systematically validated and appropriate for the clinical setting. iii.Both groups, from a community-based outpatient ambulatory center, used the same split dose regimen with Polyethylene glycol (PEG).Patients were instructed to drink 3 L of PEG preparation on the afternoon of the day prior to the exam and 1 L four hours before the scheduled exam time. All the exams scheduled for morning period. Assuming a normal distribution, a power of 90% and a type I error of 0.05, the calculated sample size for each group was 188; allowing a 10% dropout rate, the sample size is 206 per group (412 patients overall); Groups: Group A: 3-day low residue diet + split dose preparation; Group B: 1-day low residue diet + split dose preparation
d. Endoscopist:
Exams to be conduct by 5 board-certified gastroenterologists and 2 supervised fellows in training; All physicians were trained in the use of BBPS by online training available at http://cori.org/bbps/, and have been using the BBPS for at least 3 months.
e. Data collection methods: form sheet filled by the endoscopist and patient opinion regarding the assigned bowel preparation protocol.
f. Analyzed variables:
i. Primary outcome: BBPS score
ii. Secondary outcome: Patient assessment of tolerance and acceptance of the preparation and diet
iii. Tertiary outcome: polyp detection rate (PDR), polyp location, size and configuration; adenoma detection rate (ADR), cecum intubation rate
iv. Other variables and patients characteristics (age, gender, chronic medication, risk factors for inappropriate preparation), withdrawal time.
g. Statistical analysis: T-test for groups comparing quantitative variables with normal distribution (primary outcome); Qui square test for groups comparing proportions (secondary and tertiary outcomes)
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Colon Disease, Colonic Neoplasms
Keywords
Randomized controlled trial, Colonoscopy, Colon Disease, Low residue diet, Colon preparation
7. Study Design
Primary Purpose
Diagnostic
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Care Provider
Allocation
Randomized
Enrollment
412 (Actual)
8. Arms, Groups, and Interventions
Arm Title
3-day low residue diet
Arm Type
Active Comparator
Arm Description
Group A - 3 day low residue diet prior to the colonoscopy
Arm Title
1-day low residue diet
Arm Type
Placebo Comparator
Arm Description
Group B - 1 day low residue diet prior to the colonoscopy
Intervention Type
Other
Intervention Name(s)
3 day low residue diet prior to the colonoscopy
Intervention Description
3 day low residue diet prior to the colonoscopy
Intervention Type
Other
Intervention Name(s)
1 day low residue diet prior to the colonoscopy
Intervention Description
3 day low residue diet prior to the colonoscopy
Primary Outcome Measure Information:
Title
Score of mucosal visualization
Description
Using Boston Bowel Preparation Scale during the exam
Time Frame
1 day (during colonoscopy)
Secondary Outcome Measure Information:
Title
Patient assessment of diet protocol
Description
Patient assessment, by written questionnaire, of tolerance and acceptance of diet protocol.
Time Frame
1 day (the day of the exam)
Title
Polyp detection rate, location and configuration
Description
One of the quality indicators for colonoscopy is polyp detection rate, which is defined as the percentage of colonoscopies with a detection of at least one polyp. At the same time the endoscopist will assign the colonic location of the polyp (ascendent, transverse, descendent).
(PDR to be presented as %; Location to be discriminated in the endoscopist report).
Time Frame
1 day (during colonoscopy)
Title
Adenoma Detection Rate
Description
Adenoma detection rate (ADR) is the one of the strongest quality indicators for colonoscopy. This rate represents the percentage of colonoscopies with at least one adenoma identified. (to be presented as %)
Time Frame
Within 30 days from colonoscopy date
Title
Cecum intubation rate
Description
Defined as colonoscopy quality indicator the photo documentation of cecum, in at least 95% of the colonoscopies. Photo documentation of the cecum is a mark for effective total colonoscopy. (to presented as %)
Time Frame
1 day (during colonoscopy)
Title
Withdrawal time
Description
In a negative colonoscopy (no polyp identification) is defined that the withdrawal time should be at least 6 minutes for proper and safe colonic mucosa evaluation. (to be presented in minutes)
Time Frame
1 day (during colonoscopy)
Other Pre-specified Outcome Measures:
Title
Patients characteristics questionnaire
Description
Evaluate, using proper data collecting sheet, patient relevant data (age, gender, chronic medication, risk factors for inappropriate preparation)
Time Frame
1 day
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
Consecutive series of patients scheduled for total colonoscopy
Signed informed consent
Exclusion Criteria:
inpatients
sedation
urgent procedures
colonoscopies not intended to reach the caecum
patient with previous partial colectomy.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Filipe Taveira, MD
Organizational Affiliation
Portuguese Oncology Institute, Coimbra
Official's Role
Principal Investigator
Facility Information:
Facility Name
Portuguese Oncology Institute - Coimbra
City
Coimbra
ZIP/Postal Code
3001 - 651
Country
Portugal
12. IPD Sharing Statement
Plan to Share IPD
No
Citations:
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25480100
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Links:
URL
http://cori.org/bbps/
Description
BBPS training
Learn more about this trial
3-day vs. 1-day Low Residue Diet Influence in Colonoscopy Preparation and Patient Tolerability
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