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Evaluation of an Oral Sodium Sulfate Solution for Patients With Prior Difficult or Incomplete Cleansing

NCT06051955 · Status: RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 120

Last updated 2024-04-03

No results posted yet for this study

Summary

This case series aims to evaluate the effectiveness and tolerability of Oral Sulfate Solution (OSS) in patients who had previously experienced poor colonoscopy preparation.

Conditions

  • Colonoscopy
  • Bowel Preparation

Interventions

OTHER

oral sodium sulfate

All participants enrolled in this study will use Oral Sodium Sulfate as their bowel cleansing agent.

Sponsors & Collaborators

  • Pendopharm

    collaborator INDUSTRY

  • Lawrence Charles Hookey

    lead OTHER

Principal Investigators

  • Lawrence Hookey · Queen's University

Study Design

Allocation
NA
Purpose
OTHER
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2023-10-11
Primary Completion
2024-05-30
Completion
2024-09-30

Countries

  • Canada

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 NCT06051955 on ClinicalTrials.gov