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The Effect of a Predictive Model of Bowel Preparation Based on Procedure-related Factors

A

Air Force Military Medical University of People's Liberation Army

Status

Completed

Conditions

Predictive Model
Bowel Preparation
Colonoscopy

Treatments

Drug: Polyethylene glycol

Study type

Interventional

Funder types

Other

Identifiers

NCT04434625
KY20200614-3

Details and patient eligibility

About

The rate of adequate bowel preparation is one of important quality indicators of colonoscopy. Inadequate bowel preparation negatively affects the outcomes of colonoscopy. If patients with inadequate bowel preparation were identified before the procedure, enhanced strategy could be offered to achieve better bowel cleaning. Currently, there were three predicting models of inadequate bowel preparation established based on patient-related factors. So far, none of predictive models have been tested in other than their validation cohort populations, and no study has attempted to apply a different regimen to patients presenting with risk factors for inadequate colon cleanliness. In previous studies, we established a prediction model based on procedure-related factors, which has better accuracy and can better predict the quality of bowel preparation.

The aim of this study is to compare the quality of bowel preparation by using a predictive model based on procedure-related factors versus the criterion group in unsedation patients

Enrollment

900 patients

Sex

All

Ages

18 to 75 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Age: 18~75 years
  • Patients undergoing morning colonoscopy

Exclusion criteria

  • colon resection;
  • suspected bowel obstruction;
  • moderate or severe complications related to drinking the 1st or 2rd dose of PEG
  • hemodynamically unstable;
  • lactating or pregnant women;
  • no need to reach the ileocecal segment
  • unwilling to provided informed content.

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

900 participants in 2 patient groups

control group
No Intervention group
Description:
Colonoscopy was performed in the control group directly.
model-based interference group
Experimental group
Description:
Patients with score ≥3 were asked to taking another dose of PEG (1.5L) within 1-2 hours. Colonoscopy was performed in afternoon (about 4h after drinking PEG). Patients with score\<3 in IM group colonoscopy directly.
Treatment:
Drug: Polyethylene glycol

Trial contacts and locations

5

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Data sourced from clinicaltrials.gov

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