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Prospective study on the efficacy of bowel preparation with the two cup one cup method of Sulprep for total colonoscopy.

Not Applicable
Recruiting
Conditions
Colonoscopy
Registration Number
JPRN-UMIN000053562
Lead Sponsor
TT Medical Center Tokyo
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
300
Inclusion Criteria

Not provided

Exclusion Criteria

1. Gastrointestinal obstruction or suspected gastrointestinal obstruction 2. Patients with or suspected of having intestinal perforation 3. Toxic megacolonosis or suspected toxic megacolonosis 4. Patients with or suspected of having gastric evacuation disorder (gastric insufficiency paralysis) 5. Patients with intestinal stenosis or severe constipation 6. Patients with vomiting reflex disorder or those at risk of aspiration 7. Patients with a history of gastrointestinal tract surgery 8. Patients with known glucose-6-phosphate dehydrogenase deficiency 9. Patients with renal dysfunction (creatinine clearance less than 30 mL/min) 10. Persons undergoing or requiring treatment for severe cardiac disease 11. Persons at high risk of arrhythmia 12. Patients who are dehydrated 13. Persons who have been determined to have active inflammatory bowel disease during the screening phase 14. Persons under 18 years of age or over 80 years of age 15. Patients who have had hypersensitivity to any of the ingredients in Sulprep Oral Solution in the past.

Study & Design

Study Type
Observational
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Clinical utility (colon cleansing)
Secondary Outcome Measures
NameTimeMethod
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