Status:

COMPLETED

Patient Preference With Visicol Tablet Preparation for Colonoscopy

Lead Sponsor:

Mayo Clinic

Collaborating Sponsors:

InKine Pharmaceutical

Conditions:

Preparation for Colonoscopy

Eligibility:

All Genders

18+ years

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 colonosc...

Eligibility Criteria

Inclusion

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

Exclusion

  • 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

Key Trial Info

Start Date :

March 1 2005

Trial Type :

OBSERVATIONAL

Allocation :

ACTUAL

End Date :

April 1 2006

Estimated Enrollment :

53 Patients enrolled

Trial Details

Trial ID

NCT00318305

Start Date

March 1 2005

End Date

April 1 2006

Last Update

December 2 2009

Active Locations (1)

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1

Mayo Clinic

Scottsdale, Arizona, United States, 85259

Patient Preference With Visicol Tablet Preparation for Colonoscopy | DecenTrialz