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A prospective randomized controlled trial comparing the efficacy and tolerability of bowel preparation method

A prospective randomized controlled trial comparing the efficacy and tolerability of two sachets of sodium picosulphate/magnesium citrate(2SPMC), two liters of polyethylene glycol with ascorbic acid(2L PEG- ASC) in the preparation of patients for morning colonoscopy.

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CRIS
Registry ID
KCT0001228
Enrollment
250
Registered
2014-09-16
Start date
2013-03-06
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

None listed

Sponsors

Korea University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: All patients between the ages of 18 and 80 years who were scheduled to undergo colonoscopy were included.

Exclusion criteria

Exclusion criteria: (i) chronic kidney disease, (ii) severe heart failure (New York Heart Association [NYHA] class III or IV), (iii) uncontrolled hypertension (systolic pressure =170 mm Hg, diastolic pressure =100 mm Hg), (iv) severe constipation, (v) any bowel resection, (vi) significant gastroparesis, or (vii) suspected bowel obstruction or perforation.

Design outcomes

Primary

MeasureTime frame
cleansing quality of bowel preparation(Ottawa scale score, Aronchic score)—

Secondary

MeasureTime frame
patient tolerability—

Countries

Korea, Republic of

Contacts

Public ContactYoo kyung

Korea University

Outcome results

None listed

Source: CRIS (via WHO ICTRP) · Data processed: Feb 4, 2026