Status:
COMPLETED
Polyethylene Glycol Safety in Children
Lead Sponsor:
Children's Hospital of Philadelphia
Collaborating Sponsors:
Food and Drug Administration (FDA)
Conditions:
Polyethylene Glycols
Children, Only
Eligibility:
All Genders
Up to 16 years
Brief Summary
The primary objective is to measure levels of selected PEG 3350 components and metabolites in the blood and urine of children who are already taking PEG 3350 compared to children who are not taking PE...
Detailed Description
For subjects taking PEG 3350, blood and urine will be collected 1.5 to 4 hours after subjects take PEG 3350. For subjects who are not taking PEG 3350, the same PEG 3350 components and metabolites wil...
Eligibility Criteria
Inclusion
- Group 1: Children who do not have bowel or nervous system disease, or neuropsychiatric symptoms.
- Inclusion criteria:
- Children less than 17 years old who have been taking PEG 3350 for at least one month.
- Dose of PEG 3350 greater than or equal to 0.4 grams/kg/day currently recommended by the North American Society for Pediatric Gastroenterology, Hepatology and Nutrition (NASPGHAN) and European Society for Pediatric Gastroenterology, Hepatology and Nutrition (ESPGHAN) guidelines (2). Preferences will be given to children taking at least 17 grams/day.
- Normal Physical and neurological development for age. Weight and height percentiles ≥ 5% and ≤ 95% for age.
- Exclusion criteria:
- Children with underlying bowel problems that might be expected to increase bowel permeability (are included in group 2). In this group we will specifically exclude children with:
- Diarrhea within the past month. Note that PEG 3350 may cause loose stool and this is often the intended therapeutic effect. Therefore, we will exclude children with presumed infectious diarrhea since this may alter gut permeability but will include children whose loose stool is attributed to PEG 3350. If loose or watery stool began after initiation of PEG 3350 or after an increase in PEG 3350 dose within prior 3 days, children may be enrolled for GROUP 1.
- Children whose stool had a recognized diarrhea causing pathogen within the past 4 months will be excluded since the time required to repair epithelial lining is not clear. Enteric pathogens that would prevent enrollment include Salmonella, Shigella, Campylobacter, Yersinia, E. Coli (enterotoxigenic, enteropathogenic, enteraggregative, enterohemorrhagic), Clostridum difficile, Rotavirus, Norovirus, Astrovirus, and other known or suspected diarrhea causing organisms.
- H. pylori infection since this causes a stomach inflammation. HIV infection since this may alter bowel permeability (17) and predispose to other types of infection Symptoms neurologic disease or dysfunction (since they will be enrolled in Group 3).
- Group 2: Children with problems that might increase intestinal epithelial permeability.
- Inclusion criteria:
- Children less than 17 years old who have been taking PEG 3350 for at least one month.
- Dose of PEG 3350 greater than or equal to 0.4 grams/kg/day currently recommended by the NASPGHAN and ESPGHAN guidelines (2). Preferences will be given to children taking at 17 grams/day.
- c. Any of the following problems associated with increased bowel permeability:
- Weight ≤ 5% for age. Malnutrition is associated with increased intestinal permeability.
- Children who had a pathogen (see Group 1 Exclusion Criteria "A. b." for list of pathogens) isolated from their stool within the past month.
- Children with celiac disease who are untreated or began treatment within the past 3 months.
- Children with inflammatory bowel disease
- Children with Hirschsprung disease. This intestinal motility disorder predisposes to bowel injury called enterocolitis (18-20).
- Children with intestinal motility disorders other than Hirschsprung disease.
- Exclusion criteria:
- a. Children with neurologic or neuropsychiatric symptoms. These children will be enrolled in Group 3.
- Group 3: Children with underlying neurologic disease or with neuropsychiatric disorders or symptoms.
- Inclusion criteria:
- Children less than 17 years old who have been taking PEG 3350 for at least one month.
- Dose of PEG 3350 greater than or equal to 0.4 grams/kg/day currently recommended by the NASPGHAN and ESPGHAN guidelines (2). Preference will be given to children taking at least 17 grams/day.
- Any of the following problems with the nervous system:
- Diagnosed with a disease that affects nervous system function before starting PEG 3350.
- Diagnosed with a disease that affects nervous system function after starting PEG 3350.
- Abnormal nervous system function without a specific diagnosis.
- Episodic nervous system dysfunction. This might include seizure disorder, metabolic disease, or mitochondrial disease.
- Note: Included in Group 3 are children with cerebral palsy, neuronal migration defects, traumatic brain injury, hypoxic ischemic encephalopathy, seizure disorder, tics, migraine, clinical depression, anxiety disorder, obsessive-compulsive disorder, post-surgical brain injury, autism spectrum disorder as well as genetic defects that affect the nervous system (Cornelia de Lange, Rett Syndrome, Pelizaeus-Merzbacher disease, etc.).
- Any weight and height (i.e., no exclusions based on growth percentiles). Abnormalities in any organ including the bowel are acceptable.
- Exclusion criteria:
- a. There are no specific exclusion criteria. This is important since this group may be at the highest risk for PEG 3350 side effects.
- Group 4: Children who are not taking PEG 3350. We will enroll 75 children who are not taking PEG 3350. Inclusion and exclusion criteria for these children will be the same as those detailed above for children who are taking PEG 3350 except that they may not have taken PEG 3350 within the last month.
- Enrollment targets for Groups 1, 2 and 3:
- 15 children taking PEG 3350, age 0-6 years old (for each Group).
- 6 children taking PEG 3350, age 7-12 years old (for each Group).
- 4 children taking PEG 3350, age 13-17 years old (for each Group).
- An equal number of children in each age group who are not taking PEG 3350.
Exclusion
Key Trial Info
Start Date :
September 30 2022
Trial Type :
OBSERVATIONAL
Allocation :
ACTUAL
End Date :
August 9 2025
Estimated Enrollment :
158 Patients enrolled
Trial Details
Trial ID
NCT05424757
Start Date
September 30 2022
End Date
August 9 2025
Last Update
November 4 2025
Active Locations (1)
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1
Children's Hospital of Philadelphia
Philadelphia, Pennsylvania, United States, 19104