Patient Preference With Visicol Tablet Preparation for Colonoscopy

Patient Preference and Acceptance With Sodium Phosphate Tablet Preparation for Colonoscopy: A Prospective Study

Status

Completed

Phases

Unknown

Study type

Observational

Source

ClinicalTrials.gov

Registry ID

NCT00318305

Enrollment

Registered

2006-04-26

Start date

2005-03-31

Completion date

2006-04-30

Last updated

2009-12-02

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Preparation for Colonoscopy

Brief summary

The purpose of this study is to determine patient preference and acceptance of tablet sodium phosphate bowel preparation in patients who had polyethylene glycol (PEG) solution for their prior colonoscopy. This study will provide answers related to the patient preferences and their acceptance of this new method of bowel preparation.

Interventions

None listed

Study design

Observational model

CASE_ONLY

Time perspective

PROSPECTIVE

Eligibility

Sex/Gender

ALL

Age

18 Years to No maximum

Healthy volunteers

Yes

Inclusion criteria

* Prior colonoscopy with PEG solution in the past one year * Must be able to swallow tablets

Exclusion criteria

* Patients below 18 years and above 100 years. * Congestive heart failure * Chronic renal failure * Pre-existing electrolyte disorder * Pre-existing mega-colon or a motility disorder. * Patients with pre-existing seizure disorder. * Patients scheduled for colonoscopy after 1:00 p.m. will be excluded from the study. * Pregnant or lactating women

Countries

United States

Outcome results