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

NCT02536729 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 600

Last updated 2015-09-01

No results posted yet for this study

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

  • Bowel Preparation

Interventions

DRUG

Oral Sodium Phosphate - Normal preparation

DRUG

Oral sodium phosphate - Modified Preparation

DRUG

polyethylene glycol + Electrolytes

Sponsors & Collaborators

  • Tecnoquimicas S.A

    collaborator UNKNOWN

  • Fundación Salutia

    lead OTHER

Eligibility

Min Age
18 Years
Max Age
65 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2015-09-30
Primary Completion
2016-06-30

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02536729 on ClinicalTrials.gov