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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02540031
Other study ID # 2015-06-014-003
Secondary ID
Status Completed
Phase Phase 3
First received
Last updated
Start date September 2015
Est. completion date June 2018

Study information

Verified date July 2018
Source Kyungpook National University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Although adequate bowel preparation is essential for successful colonoscopy, the 23% of patients had shown inadequate bowel preparation. Inadequate bowel preparation may results in incomplete examination, increased patient's discomfort, decreased polyp detection rates, ultimately leading to repeated colonoscopies. One prior study showed that patients reporting their last rectal effluents as brown color or solid stool had a 54% chance of having fair or poor preparation. Thus, recent consensus guideline suggested consideration of additional oral preparation in patients presenting brown effluents on the day of colonoscopy. However, the data supporting additional oral preparation is still spares. Therefore, the investigators aimed to examine the impact of additional oral preparation on the quality of bowel preparation for colonoscopy in patients showing brown effluents on the day of colonoscopy.


Recruitment information / eligibility

Status Completed
Enrollment 156
Est. completion date June 2018
Est. primary completion date April 2018
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 80 Years
Eligibility Inclusion Criteria:

- patients who reporting their last rectal effluents as brown color or solid stool on the day colonoscopy

Exclusion Criteria:

- known hypersensitivity to polyethylene glycol

- severe congestive heart failure [New York Heart Association (NYHA) grade III or grade IV]

- severe renal insufficiency (creatinine clearance <30 ml/min)

- hemodynamic instability

- suspected intestinal obstruction or perforation

- compromised swallowing reflex or altered mental status

- pregnancy or lactating woman

- patients who declined to participate

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Additional oral preparation (3L of PEG+Asc, "Coolprep®")
The interventional or experimental arm will receive 1l of additional PEG+Asc, "Coolprep®" on the day of colonoscopy * Compositions/1L : Sodium Chloride 2.691g Potassium Chloride 1.015g Anhydrous sodium sulfate 7.5g PEG 3350 100g ascorbic acid 4.7g sodium ascorbate 5.9g
Standard oral preparation (2L of PEG+Asc, "Coolprep®")
The control arm will receive currently used oral preparation (2l of PEG+Asc, "Coolprep®") for colonoscopy * Compositions/1L : Sodium Chloride 2.691g Potassium Chloride 1.015g Anhydrous sodium sulfate 7.5g PEG 3350 100g ascorbic acid 4.7g sodium ascorbate 5.9g

Locations

Country Name City State
Korea, Republic of Keimyung University Dongsan Medical Center Daegu

Sponsors (1)

Lead Sponsor Collaborator
Kyungpook National University

Country where clinical trial is conducted

Korea, Republic of, 

References & Publications (1)

Fatima H, Johnson CS, Rex DK. Patients' description of rectal effluent and quality of bowel preparation at colonoscopy. Gastrointest Endosc. 2010 Jun;71(7):1244-1252.e2. doi: 10.1016/j.gie.2009.11.053. Epub 2010 Apr 1. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Quality of bowel preparation The primary outcome will be the endoscopist's assessment of the quality of preparation using a standardized bowel preparation scale Day 1
Secondary Adenoma detection rate Number of adenomatous polyps Day 1
Secondary Patient compliance Patient compliance with preparation instructions self-reported in a pre-procedure questionnaire Baseline
Secondary Patient satisfaction Patient's perception of the preparation method as self-reported on a pre-procedure questionnaire. Baseline
See also
  Status Clinical Trial Phase
Completed NCT03681444 - Diet Selection Pre-Colonoscopy: Comparison Between Clear, Low-residue and Regular Diet N/A