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2 Regimens of Lactulose for Colonoscopy Preparation in Adults

NCT01887470 · Status: COMPLETED · Phase: PHASE2 · Type: INTERVENTIONAL · Enrollment: 55

Last updated 2015-06-01

Study results available
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Summary

The purpose of the study is to determine the efficacy of 2 regimens of lactulose as a preparation for colonoscopy.

Conditions

  • Colonoscopy Preparation

Interventions

DRUG

Full dose preparation

DRUG

Split dose preparation

Sponsors & Collaborators

  • Cumberland Pharmaceuticals

    lead INDUSTRY

Principal Investigators

  • Richard Krause, M.D · ClinSearch, LLC

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
TRIPLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2013-07-31
Primary Completion
2013-10-31
Completion
2013-10-31

Countries

  • United States

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 NCT01887470 on ClinicalTrials.gov