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Clinical Trials/NCT04605432
NCT04605432CompletedNot Applicable

Face-to-face Instructions and Personalized Bowel Cleansing Regimens for Inpatients Could Improve Bowel Preparation Quality.

Ningbo No. 1 Hospital1 site in 1 country320 target enrollmentStarted: October 30, 2020Last updated:
Conditions
Interventions
Drugs

Trial Snapshot

Phase
Not Applicable
Status
Completed
Sponsor
Enrollment
320
Locations
1
Primary Endpoint
Quality of Bowel Preparation

Study Overview

Brief Summary

background:The use of enhanced instruction can improve the efficiency of education for bowel preparation regimens. Researchers hypothesized that face-to-face instruction and personalized intervention for inpatient could improve successful bowel preparation rate and patient's compliance with regimens.

Methods:This was an endoscopist-blind,randomized controlled trial. 320inpatients were randomized 1:1 in one of the two study groups. The intervention group received face-to-face instruction and personalized intervention for bowel preparation protocol, while control group received the standard bowel preparation protocol. Patients'demographics, bowel preparation quality, colonoscopy completion and attendance were recorded. Logistic regression was performed to identify predictors of bowel preparation failure.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Diagnostic
Masking
Single (Outcomes Assessor)

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Inpatients undergoing colonoscopy.
  • patients older than 18 years.

Exclusion Criteria

  • prior surgery of colorectal resection;
  • suspected colonic stricture or perforation;
  • incomplete or complete bowel obstruction;
  • use of prokinetic agents or purgatives within 7 days;
  • Patients with severe gastrointestinal diseases, such as intestinal obstruction or perforation, active ulcerative colitis, toxic colitis and toxic megacolon;;
  • pregnancy or lactation;
  • Inability to prepare bowel;
  • unable to give informed consent.

Arms & Interventions

PEG-FFI prep

Experimental

On the day before colonoscopy, an experienced researcher would go to the ward to have a face-to-face conversation with the patient to know if patients have the risk factors for bowel preparation failure.

The bowel preparation regimens for patients with risk factors would be optimized. In addition to drink single dose of 120g Polyethylene Glycol (PEG-4000) with 3L water 4-6 h before colonoscopy at a rate of 250 ml every 15 min, the patient also drink single dose of 60g Polyethylene Glycol (PEG-4000) with 1L water at 20:00- 21:00 hours on the day before the colonoscopy. Patients without risk factors drink single dose of 120g Polyethylene Glycol (PEG-4000) with 3L water 4-6 h before colonoscopy at a rate of 250 ml every 15 min.

Patients would received a booklet to explain the details of diet restriction, preparation method and the pictures of bowel preparation of results.The researcher would give a detailed oral explanation of the booklet.

Intervention: PEG-FFI (Drug)

PEG-nonFFI prep

Active Comparator

Patients in the PEG-nonFFI group would only receive routine patient education on bowel preparation of colonoscopy, which was completed by ward nurse. all the patients drink single dose of 120g Polyethylene Glycol (PEG-4000) with 3L water 4-6 h before colonoscopy at a rate of 250 ml every 15 min.

Intervention: PEG-nonFFI (Drug)

Outcomes

Primary Outcomes

Quality of Bowel Preparation

Time Frame: 1 Day of colonoscopy

The BBPS is a validated scoring system with scores between 0 and 9, where 9 is the best score. The score comprises a sub score 0-3 for each colon segment: right, transverse and left colon. For all participants, BBPS score will be used when colonscopy is withdrawing.

Secondary Outcomes

  • adverse events(The day of colonoscopy and the day before)
  • cecal intubation rate(1 Day of colonoscopy)
  • polyp detection rate(1 Day of colonoscopy)
  • cecal intubation time(1 Day of colonoscopy)
  • withdrawal time(1 Day of colonoscopy)

Investigators

Sponsor
Ningbo No. 1 Hospital
Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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