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One-Day Versus Three-Day Bowel Preparation for Colonoscopy in Children

One-Day Bowel Preparation With Polyethylene Glycol 3350 (Miralax®) is as Effective and Safe as Three-Day Preparation for Colonoscopy in Children

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02174497
Enrollment
32
Registered
2014-06-25
Start date
2008-02-29
Completion date
2010-06-30
Last updated
2014-06-25

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Bowel Preparation, Pediatric Colonoscopy

Keywords

Pediatric Colonoscopy, Bowel Preparation, Safety, Tolerability

Brief summary

This was a blinded study conducted on the efficacy and safety of a one-day versus a three-day bowel preparation in a pediatric population. Limited data is available in this regard, and this study supports the use of a one-day bowel preparation, as this is both safe and effective.

Detailed description

Colonoscopy in children and young adults is performed by gastroenterologists for a variety of indications, including but not limited to evaluation of rectal bleeding, chronic diarrhea, family history of polyposis syndromes and surveillance for colon cancer in patients with inflammatory bowel disease. A successful bowel preparation that enables clear visualization of the intestinal mucosa is essential to diagnose and treat the underlying pathology. Currently, gastroenterologists use a variety of colon cleansing preparations, but Polyethylene Glycol (PEG) 3350 given for three to four days appears to be standard. Though it is well tolerated, safe and effective the duration of preparation may cause disruption to the routine and missed school days. To date, there is limited data that shows efficacy of a shorter duration of bowel preparation with PEG. This study aims to compare the efficacy and safety of a one-day preparation with that of a three-day preparation with PEG 3350 as preparation for colonoscopy in children and young adults.

Interventions

None listed

Sponsors

St. John Health System, Michigan
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
2 Years to 21 Years
Healthy volunteers
Yes

Inclusion criteria

* Pediatric Patients referred for an outpatient colonoscopy

Exclusion criteria

* None

Design outcomes

Primary

MeasureTime frameDescription
Safety of a one day versus a three day colonoscopy preparation in a pediatric population02/08-06/10 (28 months)The Safety of the different preparations was documented by monitoring serum electrolytes before and after the preparation.

Secondary

MeasureTime frameDescription
Tolerability of a one day versus a three day colonoscopy preparation in a pediatric population02/08-06/10 (28 months)The tolerability was documented by monitoring the patient's clinical ability to consume the entire colonoscopy preparation without abdominal pain, nausea or vomiting. Furthermore, this was objectively documented by monitoring and recording the following parameters: Ease of Administration, Compliance, Willingness to take again

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 19, 2026