The Efficacy Side Effects and the Tolerance of Polyethylene Glycol 3350 as a Bowel Prep in Children
NCT ID: NCT01164410
Last Updated: 2017-10-24
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
45 participants
OBSERVATIONAL
2009-08-31
2010-06-30
Brief Summary
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Hence a Cross sectional study looking at the safety,efficacy,tolerability of PEG 3350 mixed in Gatorade G(TM) as a bowel prep in children needs to be conducted. Consent will be obtained from parents and assent will be obtained from patients. Previous laboratory tests for each patient will be reviewed. All patients in the study will be required to consume MiralaxTM/Gatorade GTM the day prior to their procedure. The patients will be given written instructions as to how to much solution to take and how to prepare and consume the solution. The patient shall be maintained on a clear liquid diet the day prior to the procedure. Once patients arrive for the colonoscopy they will be asked to complete a questionnaire regarding their bowel preparation. Prior to the administration of IV fluids, 1ml of blood will be obtained a basic metabolic panel. The patient will then undergo a colonoscopy by routine procedure and technique. The endoscopist will complete a questionnaire when done with the colonoscopy to rate the cleanliness of the colon.
We propose that MiralaxTM combined with Gatorade GTM given the day prior to colonoscopy is a safe, tolerable and efficacious cleansing regimen for colonoscopy in children.
Detailed Description
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1. Patients five years old or older that present to the pediatric GI clinic and are capable of taking oral liquids and have been scheduled for a colonoscopy.
2. Patients who are able to communicate their discomfort and preferences.
Exclusion Criteria:
1. Patients that are neurologically compromised
2. Patients in need of emergent colonoscopy
3. Patients with known metabolic, endocrine, renal or cardiac conditions.
4. Presence of pre-existing ostomy, short bowel syndrome, gastric retention, intestinal obstruction or swallowing difficulties.
5. Patients with known electrolyte abnormalities.
6. Patients who are allergic to PEG-3350.
7. Patients that are known to be pregnant.
8. Patients with known fructose intolerance.
9. Patient younger than five years old.
Conditions
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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Pediatric Colonoscopy
Patients undergoing colonoscopy in the Department of Pediatric Gastroenterology at the Cleveland Clinic Children's Hospital in Cleveland, Ohio.
No interventions assigned to this group
Eligibility Criteria
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Inclusion Criteria
* Patients who are able to communicate their discomfort and preferences.
Exclusion Criteria
* Patients in need of emergent colonoscopy
* Patients with known metabolic, endocrine, renal or cardiac conditions.
* Presence of pre-existing ostomy, short bowel syndrome, gastric retention, intestinal obstruction or swallowing difficulties.
* Patients with known electrolyte abnormalities.
* Patients who are allergic to PEG-3350.
* Patients that are known to be pregnant.
* Patients with known fructose intolerance.
* Patient younger than five years old.
5 Years
21 Years
ALL
No
Sponsors
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The Cleveland Clinic
OTHER
Responsible Party
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Locations
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Cleveland Clinic Childrens Hospital
Cleveland, Ohio, United States
Countries
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Other Identifiers
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CCF 09-378
Identifier Type: -
Identifier Source: org_study_id