Comparison of the effect of mechanical intestinal preparation with Polyethylene glycol
Not Applicable
- Conditions
- Patients under colonoscopy.
- Registration Number
- IRCT20171120037552N2
- Lead Sponsor
- Mashhad University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 100
Inclusion Criteria
To be satisfied to participate in the study .
Aged 18 to 64 years old.
At the present time, Not to be treated for liver and kidney disease.
There are no symptoms of intestinal obstruction (prolonged constipation, abdominal distension and sometimes sensitivity to touch, abdominal pain, nausea and vomiting, certain radiographic findings).
Has not History of surgery to remove all or part of the colon.
Not be Pregnant.
Not have hearing problem.
Exclusion Criteria
The Intestinal preparation protocol Completely dose not implementate.
Do not want to continue to cooperation.
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Adequacy of intestinal preparation, safety and patient acceptance under colonoscopy. Timepoint: Day of recurrences for colonoscopy and the day of colonoscopy. Method of measurement: The adequacy of intestinal preparation through the Boston instrument and the patient's acceptance through a checklist questionnaire and the safety of the patient are measured by checking blood electrolytes.
- Secondary Outcome Measures
Name Time Method