MedPath

3-day vs. 1-day Low Residue Diet Influence in Colonoscopy Preparation and Patient Tolerability

Not Applicable
Completed
Conditions
Colonic Neoplasms
Colon Disease
Interventions
Other: 3 day low residue diet prior to the colonoscopy
Other: 1 day low residue diet prior to the colonoscopy
Registration Number
NCT02955901
Lead Sponsor
Portuguese Oncology Institute, Coimbra
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)

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
412
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.

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
3-day low residue diet3 day low residue diet prior to the colonoscopyGroup A - 3 day low residue diet prior to the colonoscopy
1-day low residue diet1 day low residue diet prior to the colonoscopyGroup B - 1 day low residue diet prior to the colonoscopy
Primary Outcome Measures
NameTimeMethod
Score of mucosal visualization1 day (during colonoscopy)

Using Boston Bowel Preparation Scale during the exam

Secondary Outcome Measures
NameTimeMethod
Cecum intubation rate1 day (during colonoscopy)

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 %)

Patient assessment of diet protocol1 day (the day of the exam)

Patient assessment, by written questionnaire, of tolerance and acceptance of diet protocol.

Polyp detection rate, location and configuration1 day (during colonoscopy)

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 RateWithin 30 days from colonoscopy date

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 %)

Withdrawal time1 day (during colonoscopy)

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)

Trial Locations

Locations (1)

Portuguese Oncology Institute - Coimbra

🇵🇹

Coimbra, Portugal

© Copyright 2025. All Rights Reserved by MedPath