Trials / Unknown
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
| Type | Name | Description |
|---|---|---|
| DRUG | Oral Sodium Phosphate - Normal preparation | |
| DRUG | Oral sodium phosphate - Modified Preparation | |
| DRUG | polyethylene 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.