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Kids' laxative study reveals how body handles the drug

NCT ID NCT05424757

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Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed This study
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

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Status unknown
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First seen Jun 27, 2026 · Last updated Jun 27, 2026

Summary

This study measured levels of the laxative PEG 3350 and its breakdown products in the blood and urine of 158 children who were already taking it, compared to children not taking it. The goal was simply to learn how the body processes this medicine, not to change any treatments. Researchers also checked for any behavioral symptoms using questionnaires.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Participants

158 people

The number who actually took part.

Started

Sep 2022

Finished

Aug 2025

Lead sponsor

Other sponsor

The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Who is studied

Study population will be selected from children cared for at The Children's Hospital of Philadelphia.

Ages

0 to 16 years

Sex

Anyone

Healthy volunteers

Accepted

You do not need to have the condition being studied to take part.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

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: 1. 15 children taking PEG 3350, age 0-6 years old (for each Group). 2. 6 children taking PEG 3350, age 7-12 years old (for each Group). 3. 4 children taking PEG 3350, age 13-17 years old (for each Group). 4. An equal number of children in each age group who are not taking PEG 3350.

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Conditions

The condition(s) this trial relates to.

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Contacts and locations

Locations

  • Children's Hospital of Philadelphia

    Philadelphia, Pennsylvania, 19104, United States

More trials for these conditions

Other studies related to the condition(s) this trial covers.