Bowel Preparation Clinical Trial
Objective: The primary objective of this study is to assess the quality of life of people
treated with oral phosphate compared with polyethylene glycol + electrolytes to imaging
procedures, according to the outcome variables reported by patients.
Type of study: A non-interventional observational analytic prospective cohort study.
Sample: We will include people who need bowel cleansing for the realization of imaging tests
Exposures: - oral sodium phosphate normal regimen
- Oral sodium phosphate with modified diet
- Polyethylene Glycol + electrolytes
Follow-up time: 8 days after the bowel preparation
Outcomes: Boston Scale measure Safety Differences between groups in blood test (Sodium,
Potassium, Calcium)
n/a
Observational Model: Cohort, Time Perspective: Prospective
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