Comparative study of transenteral bowel preparation and peroral preparation for colonoscopy

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

CRIS

Registry ID

KCT0001136

Enrollment

224

Registered

2014-06-16

Start date

2013-05-13

Completion date

Unknown

Last updated

2019-03-11

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Interventions

Others : ?Participants allocated to control group (peroral preparation group)were required to drink 1L solution of poloyethylene glycol and ascorbic acid from 10 o’clock the day before scheduled colon

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: 1)people who was between 18 and 75 years of age. 2)people who has at least 3 times per week of spontaneous bowel motility

Exclusion criteria

Exclusion criteria: 1)patient with surgical abdomen 2)patient with active inflammation of bowel 3)patient with bowel obstruction or ileus 4)patient with acute peptic ulcer 5)patient with cardiac disease - cardiac arrhythmia, uncontrolled angina, acute myocardial infarction within recent three months, congestive heart failure 6) patient with renal failure or electrolyte imbalance 7) patient with history of colorectal or gastrointestinal surgery

Design outcomes

Primary

Measure	Time frame
Degrees of comfort of both modailties of bowel preparation;preference to both modalities of bowel preparation	—

Secondary

Measure	Time frame
grades of bowel preparation;polyp detection rate;colonoscopic insertion time;adverse events of both modalities of bowel preparation	—

Countries

Korea, Republic of

Contacts

Public ContactSung-Won Jung

Hallym University Medical Center-Kangnam

Outcome results