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Study of Different Endoscopic Preparations Used in Pediatric Colonoscopy

NCT04153084 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 126

Last updated 2019-11-08

No results posted yet for this study

Summary

The aim of this study is to evaluate the quality, acceptance, tolerability and adverse effects of colonoscopy preparations with the different available preparation guidelines.

Conditions

  • Digestive Illness

Interventions

DRUG

Polyethylene Glycol 4000 with electrolytes

The high volume electrolytes PEG will be administered at a 4 mg/kg dose the day before the procedure in 4-8 hours.

DRUG

PEG-3350 with electrolytes

The low volume electrolytes PEG will be administered at a 4 mg/kg dose the day before the procedure in 4-8 hours.

DRUG

Sodium picosulfate

The Sodium picosulfate will be administered the day before the procedure at different doses depending on the patient´s age: * From 1 to 2 years old: ¼ sachet reconstituted in ¼ glass of water/juice in the afternoon (15:00 h) and ¼ sachet reconstituted in ¼ glass of water/juice 6 hours later (21:00 h) * From 2 to 4 years old: ½ sachet in ½ glass of water/juice in the afternoon and ½ sachet in ½ glass of water/juice at night. * From 4 to 9 years old: 1 sachet in 1 glass of water/juice in the afternoon and ½ sachet in ½ glass of water/juice at night. * Of 9 years old and older: 1 sachet in the afternoon and 1 sachet at night.

Sponsors & Collaborators

  • Fundación Pública Andaluza para la gestión de la Investigación en Sevilla

    lead OTHER

Principal Investigators

  • Alejandro Rodríguez Martínez · Hospital Universitario Virgen Rocío

Eligibility

Min Age
1 Year
Max Age
16 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2018-10-01
Primary Completion
2019-12-15
Completion
2019-12-31

Countries

  • Spain

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04153084 on ClinicalTrials.gov