Clinical Trials Directory

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UnknownNCT02536729

Evaluation of the Quality of Life of Patients Requiring Intestinal Cleansing Using Oral Medications to Imaging Procedure by Patient Reported Outcome

Status
Unknown
Phase
Study type
Observational
Enrollment
600 (estimated)
Sponsor
Fundación Salutia · Academic / Other
Sex
All
Age
18 Years – 65 Years
Healthy volunteers
Not accepted

Summary

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)

Conditions

Interventions

TypeNameDescription
DRUGOral Sodium Phosphate - Normal preparation
DRUGOral sodium phosphate - Modified Preparation
DRUGpolyethylene glycol + Electrolytes

Timeline

Start date
2015-09-01
Primary completion
2016-06-01
First posted
2015-09-01
Last updated
2015-09-01

Source: ClinicalTrials.gov record NCT02536729. Inclusion in this directory is not an endorsement.