Preparation for Colonoscopy Clinical Trial
Official title:
Patient Preference and Acceptance With Sodium Phosphate Tablet Preparation for Colonoscopy: A Prospective Study
Verified date | December 2009 |
Source | Mayo Clinic |
Contact | n/a |
Is FDA regulated | No |
Health authority | United States: Institutional Review Board |
Study type | Observational |
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.
Status | Completed |
Enrollment | 53 |
Est. completion date | April 2006 |
Est. primary completion date | April 2006 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | Both |
Age group | 18 Years and older |
Eligibility |
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 |
Observational Model: Case-Only, Time Perspective: Prospective
Country | Name | City | State |
---|---|---|---|
United States | Mayo Clinic | Scottsdale | Arizona |
Lead Sponsor | Collaborator |
---|---|
Mayo Clinic | InKine Pharmaceutical |
United States,
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