A Safety and Efficacy Evaluation of 3 Bowel Preparations in the Pediatric Population

Inclusion criteria

• Male or female patients who are undergoing colonoscopy for a routinely accepted indication, including:

• Evaluation of BE results
• Endosonography
• Blood in stool
• Anemia of unknown etiology
• Abdominal Pain
• Polypectomy
• Unknown diarrhea or constipation etiology
• Inflammatory bowel disease
• Between 6 and 16 years of age at screening.
• Otherwise in good health, as determined by physical exam and medical history.
• If female, and of child-bearing potential, is using an acceptable form of birth control (hormonal birth control, IUD, double-barrier method, depot contraceptive, sterilized, abstinent, or vasectomized spouse).
• Negative urine pregnancy test at screening, if applicable
• In the investigator's judgment, parent/guardian is mentally competent to provide informed consent to participate in the study.

Exclusion criteria

• Subjects with known or suspected ileus, gastrointestinal obstruction, gastric retention, bowel perforation, toxic colitis, or toxic megacolon
• Subjects impacted at screening
• Subjects with impaired consciousness that predisposes them to pulmonary aspiration.
• Subjects who are undergoing colonoscopy for foreign body removal and decompression
• Subjects with known difficulties for swallowing tablets
• Subjects with pre-existing electrolyte disturbances, such as dehydration, or those secondary to the use of diuretics.
• Subjects who are taking drugs that may affect electrolyte levels with the exception of routine diuretics.
• Subjects with known clinically significant electrolyte abnormalities such as hypernatremia, hyperphosphatemia, hypokalemia, or hypocalcemia
• Subjects who are pregnant or lactating, or intending to become pregnant during the study.
• Subjects of childbearing potential who refuse a pregnancy test.
• Subjects who are allergic to any preparation components
• Subjects who, in the opinion of the investigator, should not be included in the study for any reason, including inability to follow study procedures.
• Subjects who have participated in an investigational clinical, surgical, drug, or device study within the past 30 days.
• Any condition in parent/guardian associated with poor subject compliance (e.g., substance abuse); inability of parent/guardian to return for scheduled visits with their child.