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NCT06666556CompletedPhase 4

Bowel Preparation in Colonoscopy: Lactulose vs Polyethyleneglycol, Randomized Double-blind Comparative Clinical Trial, Multicenter Study.

Source: ClinicalTrials.gov · Last updated 28 Jul 2026

Brief summary (registry, in English)

The goal of this clinical trial it is to bowel the instestinal preparation with lactulose vs poliethylenglicol as better agent to have a quality colonoscopy and demostrate that lactulose is most efective, has a good tolerance and the patient would have a better satisfaction, so the question is: wich is the eficancy of lactulose in comparision with thepoliethylenglycol in the intestinal preparation for the colonoscopy?

Status (registry)
Completed
Phase (registry)
Phase 4
Study type
Interventional
Enrollment
449 (actual)
First submitted
28 Oct 2024
Start date
20 Jul 2024
Primary completion date
31 Jul 2025
Lead sponsor
Hospital Civil de Guadalajara
NCT number
NCT06666556

What you commit to

  • Study type: Interventional · Phase 4
  • Participants enrolled: 449
  • From 20 Jul 2024 to the primary completion date, 31 Jul 2025
  • 3 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study design.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • Patients with a medical record of colonic resection, ostomy status, severe cardiopulmonary and renal diseases, major psychiatric disorders, therapeutic colonoscopy or any contraindications for colonoscopy
  • Active bleeding during the procedure
  • Patients with a known diagnosis of colorectal cancer

Age

  • Patients under 18 or over 80 years old

Other

  • All patients that won´t like to participate in the protocol or won´t sign the informed consent
  • Pregnant women
  • Non compliance with the colonic preparation regimen

Criteria the registry did not label

  • Inclusion Criteria:
  • Patients with indication for colonoscopy in our coloproctology service
  • Both women and men
  • Patients within an age range of 18-79 years
  • Patients who agree having a colonoscopy and who sign the informed consent to participate in the protocol

Age in the registry: 18 years to 79 years · Sex: All · Accepts healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (3)

Sites in registry order. Save your city in your profile to sort them by distance.

SiteCityCountrySite status
Nuevo Hospital Civil de Guadalajara "Juan I. Menchaca"
Coordinator of this site? Confirm its status
GuadalajaraMexicoUnknown status
Antiguo Hospital Civil de Guadalajara "Fray Antonio Alcalde"
Coordinator of this site? Confirm its status
GuadalajaraMexicoUnknown status
IMSS Hospital General Regional 220 "José Vicente Villada"
Coordinator of this site? Confirm its status
MéxicoMexicoUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.